CA2266543C - Methods and compositions for identifying receptor effectors - Google Patents

Methods and compositions for identifying receptor effectors Download PDF

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CA2266543C
CA2266543C CA002266543A CA2266543A CA2266543C CA 2266543 C CA2266543 C CA 2266543C CA 002266543 A CA002266543 A CA 002266543A CA 2266543 A CA2266543 A CA 2266543A CA 2266543 C CA2266543 C CA 2266543C
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yeast
receptor
gene
assay
cell
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CA2266543A1 (en
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Joshua Trueheart
Jeremy I. Paul
Hans A. Fuernkranz
Debra Nathan
Scott Holmes
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Cadus Pharmaceutical Corp
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    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q1/00Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/02Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving viable microorganisms
    • C12Q1/025Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving viable microorganisms for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K14/00Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/37Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from fungi
    • C07K14/39Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from fungi from yeasts
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09Recombinant DNA-technology
    • C12N15/63Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
    • C12N15/79Vectors or expression systems specially adapted for eukaryotic hosts
    • C12N15/80Vectors or expression systems specially adapted for eukaryotic hosts for fungi
    • C12N15/81Vectors or expression systems specially adapted for eukaryotic hosts for fungi for yeasts
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q1/00Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6897Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids involving reporter genes operably linked to promoters

Abstract

The present invention makes available a rapid, effective assay for screening and identifying pharmaceutically effective compounds that specifically interact with and modulate the activity of a cellular protein, e.g., a receptor or ion channel. The subject assay enables rapid screening of large numbers of compounds to identify those which act as an agonist or antagonist to the bioactivity of the cellular protein. The subject assay is particularly amenable for identifying surrogate ligands for receptors especially from small molecule or peptide libraries or from peptides produced by an autocrine system. Identification can be achieved via activation of a yeast signalling pathway, specially the yeast pheromone system pathway.

Description

CPI-031 C2PC , METHODS AND COMPOSITIONS FOR IDENTIFYING
RECEPTOR EFFECTORS
s Background OjThe Invention The identification of biological activity in new molecules has historically been accomplished through the use of in vitro assays or whole animals. Intact biological entities, either cells or whole organisms, have been used to screen for anti-bacterial, anti-fungal, anti-parasitic and anti-viral agents in vitro. Cultured mammalian cells have also io been used in screens designed to detect potential therapeutic compounds. A
variety of bioassay endpoints have been exploited in cell screens including the stimulation of growth or differentiation of cells, changes in cell motility, the production of particular metabolites, the expression of specific proteins within cells, altered protein function, and altered conductance properties. Cytotoxic compounds used in cancer chemotherapy is have been identified through their ability to inhibit the growth of tumor cells in vitro and in vivo. In addition to cultures of dispersed cells, whole tissues have served in bioassays, as in those based on the contractility of muscle.
In vitro testing is a preferred methodology in that it permits the design of high throughput screens: small quantities of large numbers of compounds can be tested in a
2 o short period of time and at low expense. Optimally, animals are reserved for the latter stages of compound evaluation and are not used in the discovery phase; the use of whole animals is labor-intensive and extremely expensive.
The search for agonists and antagonists of cellular receptors has been an intense area of research aimed at drug discovery due to the elegant specificity of these molecular 2 s targets. Drug screening has been carried out using whole cells expressing functional receptors (Manfredi, J.P. et al. (1996) Molecular and Cellular Biology 16(9):4700-4709) and, recently, binding assays employing membrane fractions or purified receptors have been designed to screen compound libraries for competitive ligands.
The heterologous expression of recombinant mammalian G protein-coupled a o receptors in mammalian cells which do not normally express those receptors has been described as a means of studying receptor function for the purpose of identifying agonists and antagonists of those receptors. For example, the human muscarinic receptor (HM 1 ) has been functionally expressed in mouse cells (Harpold et al. US Pat.
5,401,629). The rat V lb vasopressin receptor has been found to stimulate
3 s phosphotidylinositol hydrolysis and intracellular Ca2+ mobilization in Chinese hamster ovary cells upon agonist simulation (Lolait et al. (1995) Proc Nat1 Acad Sci.
USA
92:6783-6787). These types of ectopic expression studies have enabled researchers to AMENDED SHEET

study receptor signaling mechanisms and to perform mutagenisis studies which have been useful in identifying portions of receptors that are critical for ligand binding or signal transduction.
Experiments have also been undertaken to express functional G protein coupled receptors in yeast cells. For example, U.S. Patent 5,482,835 to King et al.
describes a transformed yeast cell which is incapable of producing a yeast G protein a subunit, but which has been engineered to produce both a mammalian G protein a-subunit and a mammalian receptor which is "coupled to" (i.e., interacts with) the aforementioned mammalian G protein a-subunit. Specifically, U.S. Patent 5,482,835 reports expression of the human beta-2 adrenergic receptor ((32AR), a seven transmembrane receptor (STR), in yeast, under control of the GAL 1 promoter, with the (32AR gene modified by replacing the first 63 base pairs of coding sequence with 11 base pairs of noncoding and 42 base pairs of coding sequence from the STE2 gene. (STE2 encodes the yeast a-factor receptor). The Duke researchers found that the modified ~32AR was functionally integrated into the membrane, as shown by studies of the ability of isolated membranes to interact properly with various known agonists and antagonists of (32AR. The ligand binding affinity for yeast-expressed ~32AR was said to be nearly identical to that observed for naturally produced ~i2AR.
U.5. Patent 5,482,835 describes co-expression of a rat G protein a-subunit in the same cells, yeast strain 8C, which lacks the cognate yeast protein. Ligand binding resulted in G protein-mediated signal transduction. U.5. Patent 5,482,835 teaches that these cells may be used in screening compounds for the ability to affect the rate of dissociation of Ga from G(3y in a cell. For this purpose, the cell further contains a pheromone-responsive promoter (e.g. BAR 1 or FUS I ), linked to an indicator gene (e.g.
HIS3 or LacZ). The cells are placed in mufti-titer plates, and different compounds are placed in each well. The colonies are then scored for expression of the indicator gene.
Summary of the Invention The present invention relates to novel, rapid, reliable and effective assays for screening and identifying pharmaceutically effective compounds that specifically interact with and modulate the activity of a cellular receptor or ion channel of a cell.
The present invention provides for the use of any type of cell in the subject assays, whether prokaryotic or eukaryotic. In preferred embodiments, the cells of the present invention are eukaryotic. In certain preferred embodiments the cells are mammalian cells. In other preferred embodiments the cells are yeast cells, with cells from the genera Saccharomyces or Schizosaccharomyces being more preferred. The host cells can be derived from primary cells, or transformed and/or immortalized cell lines.
The subject assays provide a means for detecting the ability of compounds to modulate the signal transduction activity of the target receptor by scoring for up or down-regulation of a detection signal. Signal trasduction can be measured in a variety of ways. For example, endogenous yeast second messenger generation (e.g., GTP
hydrolysis, calcium mobilization, or phospholipid hydrolysis) or increased transcription of an endogenous gene can be detected directly. Alternatively, the use of a reporter or indicator gene can provide a convenient readout. By whatever means measured, a change (e.g., a statistically significant change) in the detection signal can be used to facilitate isolation of those cells from the mixture which have received a signal via the target receptor, and thus can be used to identify novel compounds which function as receptor agonists or antagonists.
In one embodiment of the present invention the reagent cells express the receptor of interest endogenously. In other embodiments, the cells are engineered to express a heterlogous receptor protein. In either of these embodiments, it may be desirable to inactivate one or more endogenous genes of the host cells. For example, certain preferred embodiments in which a heterlogous receptor is provided utilize host cells in which the gene for the homologous receptor has been inactivated. Likewise, other proteins involved in transducing signals from the target receptor can be inactivated, or complemented with an ortholog or paralog from another organism, e.g., yeast G
protein subunits can be complemented by mammalian G protein subunits in yeast cells also engineered to express a mammalian G protein coupled receptor. Other complementations include, for example, expression of heterologous MAP kinases or erk kinases, MEKs or MKKs (MAP kinase kinases), MEKKs (MEK kinases), ras, raf, STATs, JAKs and the like.
In one embodiment, the assay of the present invention can be used to screen compounds which are exogenously added to cells in order to identify potential receptor effector compounds. In another embodiment the subject assays enable rapid screening of large numbers of polypeptides in a library expressed in the cell in order to identify those polypeptides which agonize or antagonize receptor bioactivity, creating an autocrine system. The autocrine assay is characterized by the use of a library of recombinant cells, each cell of which includes a target receptor protein whose signal transduction activity can be modulated by interaction with an extracellular signal, the transduction activity being able to generate a detectable signal, and an expressible recombinant gene encoding an exogenous test polypeptide from a polypeptide library.
By the use of a gene library, the mixture of cells collectively express a population of test
-4-polypeptides. In preferred embodiments, the polypeptide library includes at least 103 different polypeptides, though more preferably at least 105, 106, or 10' different (variegated) polypeptides. The polypeptide library can be generated as a random peptide library, as a semi-random peptide library (e.g., based on combinatorial mutagenesis of a known ligand), or as a cDNA library.
In another embodiment of the assay, if a test compound does not appear to directly induce the activity of the receptor protein, the assay may be repeated and modified by the introduction of a step in which the cell is first contacted with a known activator of the target receptor to induce the signal transduction pathways from the receptor. Thus, a test compound can be assayed for its ability to antagonize, e.g., inhibit or block the activity of the activator.
Alternatively, the assay can score for compounds which potentiate the induction response generated by treatment of the cell with a known activator. As used herein, an "agonist" refers to agents which either induce activation of receptor signaling pathways, e.g., such as by mimicking a ligand for the receptor, as well as agents which potentiate the sensitivity of the receptor to a ligand, e.g., lower the concentrations of ligand required to induce a particular level of receptor-dependent signaling.
In one aspect, the invention pertains to an assay for identifying a compound that modulates a heterologous receptor expressed by a yeast cell. The subject assays comprise the steps of: (i) providing a yeast cell in which a heterologous receptor is functionally integrated into an endogenous yeast signaling pathway, wherein said yeast cell comprises an endogenous gene operatively linked to a heterologous promoter at the natural location of said endogenous gene in said yeast cell, said promoter being responsive to signals produced by said yeast signaling pathway; (ii) contacting the yeast cell with a test compound; and (iii) detecting an alteration in a signal produced by the endogenous yeast signaling pathway thereby identifying a compound that modulates the heterologous receptor.
The invention also provides an assay for identifying a compound that modulates a heterologous orphan G protein-coupled receptor expressed by a yeast cell comprising:
i) providing a yeast cell which expresses a heterologous orphan G protein-coupled receptor which is functionally integrated into an endogenous yeast signaling pathway, wherein said yeast cell comprises an endogenous gene operatively linked to a heterologous promoter at the natural location of said endogenous gene in said yeast cell, said promoter being responsive to signals produced by said yeast signaling pathway;

- 4a-ii) contacting the yeast cell with a non-peptidic test compound; and iii) detecting an alteration in a signal produced by the endogenous yeast gene;
to thereby identify a non-peptidic compound that modulates the heterologous orphan G-protein coupled receptor.
The invention further provides an assay for identifying a compound that modulates a heterologous receptor expressed by a yeast cell comprising:
i) providing a yeast cell which expresses a heterologous receptor which is functionally integrated into an endogenous yeast pheromone response pathway, wherein said yeast cell comprises an endogenous gene operatively linked to a heterologous promoter at the natural location of said endogenous gene in said yeast cell, said endogenous gene encoding a protease, and said promoter being responsive to signals produced by said pheromone response pathway;
ii) contacting the yeast cell wit a test compound; and iii) detecting an alteration in a signal produced by the protease; to thereby identify a compound that modulates the heterologous receptor.
The invention additionally provides an assay for identifying a compound that modulates a human FPRL-1 receptor expressed by a yeast cell comprising:
i) providing a yeast cell which expresses a human FPRL-1 receptor which is functionally integrated into an endogenous yeast signaling pathway;
ii) contacting the yeast cell with a non-peptidic test compound; and iii) detecting an alteration in a signal produced by the endogenous yeast signaling pathway;
to thereby identify a non-peptidic compound that modulates a human FPRL-1 receptor.
In preferred embodiments, the signaling pathway is a yeast pheromone system pathway.
In other preferred embodiments, the step of detecting comprises measuring the transcription of a gene which encodes an endogenous yeast protein. The transcription of a gene can be measured directly or indirectly. In addition, in other embodiments, the amount or activity of an endogenous yeast protein can be assayed.
The compounds to be tested in the subject assays can be derived from a number of sources. In a preferred embodiment, the test compound is derived from a peptide library. In another preferred embodiment, the test compound is derived from a library of non-peptidic compounds.

- 4b-In the embodiments of the subject assays in which the activity of an endogenous yeast protein is assayed, the endogenous yeast protein can be encoded by an endogenous yeast gene which is operatively linked to a promoter which is responsive to signals produced by a yeast pheromone system. In one embodiment, the promoter is naturally
-5-occurring. In yet another embodiment, the promoter is non-naturally occurring.
Such non-naturally occurring promoters can be derived by modifying a naturally-occurring promoter, e.g., by mutating a naturally-occurring promoter. In yet other embodiments of the assay, the promoter is a heterologous promoter operatively linked to the endogeneous yeast gene.
In preferred embodiments, the endogenous yeast gene to be assayed is the BAR1 gene. In other preferred embodiments, the promoter which regulates expression of the endogenous yeast gene is a pheromone responsive promoter. Examples of preferred pheromone-responsive promoters include the Fusl promoter and the Fus 2 promoter, which, in certain embodiments, are operatively linked to a heterologous endogenous gene.
In yet another embodiment, the subject assays utilize yeast cells which comprise a chimeric nucleic acid construct. This chimeric construct encodes a fusion protein that modulates the expression of an endogenous gene, wherein this expression is assayable.
The chimeric constructs of the invention comprise a first segment derived from a first gene, which encodes a polypeptide that is activated by the yeast pheromone system pathway, and a second segment which encodes a polypeptide that binds a DNA
sequence in the regulatory region of an endogenous gene of interest. Such constructs render the gene of interest responsive to activation by the yeast pheromone system pathway.
In preferred embodiments, the first segment of such a construct encodes Ste 12.
In other preferred embodiments, the second segment encodes Pho4 (or a DNA
binding domain thereof). In yet another preferred embodiment, the endogenous yeast gene to be assayed is a PhoS gene (which contains a Pho4 binding site within its regulatory region).
Thus, upon expression of the Ste 12-Pho4 fusion protein (whose expression is pheromone responsive), the fusion protein binds to the Pho4 site in the PhoS
gene, thereby activating expression of the PhoS gene. The PhoS gene encodes an acid phosphatase whose expression is readily assayable. In a particularly preferred embodiment, the first segment of the chimeric construct encodes a polypeptide comprising amino acids 1-688 of Ste 12. In another particularly preferred embodiment, the second segment encodes a polypeptide comprising amino acids 227-312 of Pho4. In yet another preferred embodiment, the yeast cell to be used in the assay also comprises a mutation in its endogenous Pho4 gene. In a preferred embodiment, the detecting step of an assay of the present invention comprises detecting the activity of PHOS
acid phosphatase.
In yet another embodiment of the subject assays, the detecting step comprises detecting a change in the activity of an endogenous enzyme expressed by said yeast cell -b-m response to a signal produced by the endogenous yeast signaling pathway.
Preferably, the endogenous yeast signaling pathway is a yeast pheromone system pathway. A
change in the activity of an endogenous enzyme can be detected by, for example, measuring the enzymatic activity of the enzyme. In a preferred embodiment, the assay comprises detecting the activity of BARI protease.
The activity of BAR1 protease can be detected in a variety of ways. For example, the cleavage of a substrate having a BAR1 peptide recognition sequence can be monitored. In a preferred embodiment, the BAR1 substrate comprises at least one detectable label. In one embodiment, the substrate is naturally occurring. In yet another embodiment, the substrate is not naturally occurring. In a preferred embodiment, the substrate comprises the compound of SEQ ID N0:4. In yet another preferred embodiment the substrate comprises the compound of SEQ ID NO:S.
In still another embodiment, the substrate is a chimeric substrate comprising a first polypeptide which, upon cleavage by BARI, exposes an amino terminal Lys;
and a second polypeptide linked to the carboxy terminus of said first polypeptide.
In a particularly preferred embodiment the step of detecting comprises measuring the stability of the chimeric substrate.
BARI activity also can be detected by measuring the effect of the enzyme on the growth of a test yeast strain which does not express a functional BAR1 enzyme.
Thus, medium from BARI-expressing cells that have been contacted with a test compound can be cultured with the test yeast strain to thereby detect the presence of BAR1 activity in the medium.
In another aspect, the invention provides an assay for identifying a compound that modulates a receptor in a cell comprising the steps of (i) providing a cell which expresses a receptor which is functionally integrated into an endogenous signaling pathway of the cell; (ii) contacting the cell with a library of non-peptidic compounds;
and (iii) detecting an alteration in a signal produced by the endogenous signaling pathway. In a preferred embodiment, the cell is a yeast cell. In yet another preferred embodiment, the signaling pathway is a yeast pheromone system pathway. The step of measuring can comprise, for example, measuring the transcription of an endogenous gene or the activity of an endogenous protein in the cell.
In another aspect, the invention privides an assay for identifying a compound that modulates a receptor in a cell comprising the steps of (i) providing a cell which expresses a receptor which is functionally integrated into an endogenous signaling pathway of the cell; (ii) contacting the cell with a library of test polypeptides, wherein said library of test polypeptides is expressed by the cell; and (iii) detecting an alteration in a signal produced by the endogenous signaling pathway. In a preferred embodiment, _'7_ the cell is a yeast cell. In yet another preferred embodiment, the signaling pathway is a yeast pheromone system pathway. The step of measuring can comprise, for example, measuring the transcription of an endogenous gene or the activity of an endogenous protein in the cell.
In yet another aspect the invention provides an assay for identifying a compound that modulates a pheromone system protein surrogate in a yeast cell comprising the steps of: (i) providing a yeast cell which comprises a pheromone system protein surrogate which is functionally integrated into an endogenous pheromone system signaling pathway of the yeast cell; (ii) contacting the cell with a library of non-peptidic compounds; and (iii) measuring an alteration in a signal produced by the endogenous pheromone signaling pathway of the yeast cell.
In a preferred embodiment, the step of measuring comprises measuring the transcription of an endogenous gene or the activity of an endogenous protein in the cell.
In a preferred embodiment, the pheromone system protein surrogate to be assayed is selected from the group consisting of G protein-coupled receptors, G proteins, proteases, kinases, farnesyltransferases, carboxymethyltransferases, ABC transporters and cyclins.
In another aspect, the invention provides an assay for identifying a compound that modulates a pheromone system protein surrogate in a yeast cell comprising the steps of: (i) providing a yeast cell which comprises a pheromone system protein surrogate which is functionally integrated into an endogenous pheromone system signaling pathway of the yeast cell; (ii) contacting the cell with a library of test polypeptides, wherein said library of test polypeptides is expressed by the cell; and (iii) measuring an alteration in a signal produced by the endogenous pheromone signaling pathway of the yeast cell.
In a preferred embodiment, the step of measuring comprises measuring the transcription of an endogenous gene or the activity of an endogenous protein in the cell.
In a preferred embodiment, the pheromone system protein surrogate to be assayed is selected from the group consisting of G protein-coupled receptors, G proteins, proteases, kinases, farnesyltransferases, carboxymethyltransferases, ABC transporters and cyclins.
The invention also provides substrates for a BAR1 enzyme. In preferred embodiments, the substrate comprises the compound of SEQ ID NO: 4 or SEQ ID
NO:S.
The invention also provides a chimeric substrate for a BAR1 enzyme, the chimeric substrate comprising: a first polypeptide segment derived from mature yeast a-factor and a second polypeptide segment derived from a second, different polypeptide, wherein upon cleavage of said first polypeptide segment by BARI a change in the stability of said second polypeptide segment is detectable.

_g_ In preferred embodiments, the second polypeptide segment is derived from LacZ. In yet another preferred embodiment, the second polypeptide segment is derived from a protein which is essential for yeast cell growth. In yet another preferred embodiment the second polypeptide segment is derived from a yeast repressor protein.
In another aspect the invention provides a chimeric nucleic acid construct comprising: a first segment comprising an nucleotide sequence encoding a polypeptide which is activated by a yeast pheromone system pathway; and a second segment comprising a nucleotide sequence encoding a Pho4 polypeptide. In a preferred embodiment the first segment encodes a Ste 12 polypeptide.
The invention also provides a yeast cell which comprises a chimeric nucleic acid construct of the invention.
Receptor proteins for use in the present invention can be any receptor or ion channel which interacts with an extracellular molecule (i.e. hormone, growth factor, peptide, ion) to modulate a signal in the cell. To illustrate the receptor can be a cell surface receptor, or in other embodiments can be an intracellular receptor. In preferred embodiments, the receptor is a cell surface receptor, such as: a receptor tyrosine kinase, e.g., an EPH receptor; an ion channel; a cytokine receptor; an multisubunit immune recognition receptor, a chemokine receptor; a growth factor receptor, or a G-protein coupled receptor, such as a chemoattracttractant peptide receptor, a neuropeptide receptor, a light receptor, a neurotransmitter receptor, or a polypeptide hormone receptor.
Preferred G protein coupled receptors include: a 1 A-adrenergic receptor, oc 1 B-adrenergic receptor, a2-adrenergic receptor, a,2B-adrenergic receptor, (31-adrenergic receptor, X32-adrenergic receptor, (33-adrenergic receptor, m 1 acetylcholine receptor (AChR), m2 AChR, m3 AChR, m4 AChR, m5 AChR, D 1 dopamine receptor, D2 dopamine receptor, D3 dopamine receptor, D4 dopamine receptor, DS dopamine receptor, A 1 adenosine receptor, A2b adenosine receptor, 5-HT 1 a receptor, 5-HT1 b receptor, SHT1-like receptor, 5-HTld receptor, SHTId-like receptor, SHTld beta receptor, substance K (neurokinin A) receptor, fMLP receptor, fMLP-like receptor, angiotensin II type 1 receptor, endothelin ETA receptor, endothelin ETB
receptor, thrombin receptor, growth hormone-releasing hormone (GHRH) receptor, vasoactive intestinal peptide receptor, oxytocin receptor, somatostatin SSTR1 and SSTR2, SSTR3, cannabinoid receptor, follicle stimulating hormone (FSH) receptor, leutropin (LH/HCG) receptor, thyroid stimulating hormone (TSH) receptor, thromboxane A2 receptor, platelet-activating factor (PAF) receptor, CSa anaphylatoxin receptor, Interleukin 8 (IL-8) IL-BRA, IL-8RB, Delta Opioid receptor, Kappa Opioid receptor, mip-1/RANTES
receptor, Rhodopsin, Red opsin, Green opsin, Blue opsin, metabotropic glutamate mGluRl-6, histamine H2 receptor, ATP receptor, neuropeptidt Y receptor, arnyloid protein precursor receptor, insulin-like growth factor Il receptor, bradykinin receptor, gonadotropin-releasing hormone receptor, cholecystokinin receptor, melanocyte stimulating hormone receptor. antidiuretic hormone receptor, g1 ucagon receptor, and adrenoconicotropic hormone II receptor.
Preferred I=PH receptors include eph, elk, eck, sek, mek4, hek, hrk2, eek, erk, ryrol, ryroa, ryro5, ryro6, ryroll, cek.~, cek5, cek6, cek7, cek8, cek9, cekl0, bsk, rtkl, rrk,2, rrk3, mykl, rr~yk2, ehkl, ehk2, pagliaccio, hrk, erk and nuk receptors.
In addition, the subject assay can be used to identifying ligands for an orphan receptor, i.e., a receptor with no known ligand, regardless of the class of receptors to which it belongs.
In those embodiments wherein the target receptor is a cell surface receptor, and the cell expresses a peptide library, in certain embodiments, it will be desirable for the peptides in the library to express a signal seduence to ensure chat they are processed in the appropriate secretory pathway and thus are available to interact with receptors on the cell surface.
In other embodiments, the host cell harbors a reporter construct containing a reporter gene in operative linkage with one or more tcanseriptional regulatory elements responsive to the signal transduction activity of the receptor protein.
Exemplary reporter genes include en2ymes, seen as luciferase, phosphatase, or ~3-galactosidase which can produce a specuometrieally active label, e.g.. changes in color, fluorescence or luminescence, or a gene product which alters a cellular phenotype, e.g., cell growth, drug resistance or auxotrophy. In preferred embodiments: the reporter gene encodes a gene product selected from the group consisting of chloramphenicol acetyl transferase, beta-galactosidase and secreted alkaline phosphatase. In still other embodiments, the reporter gene encodes a gene product which confers a growth signal. In yet other embodiments, the reporter gene encodes a gene product for growth in media containing aminotriazole or canavanine or cycloheximide.
.Brief Description of tire Draf,~ings Figure 1 is a sequence alignment ofN-terminal rCgions ofCa subunits and N-terminal sequences of GPA41-Ga hybrid proteins.
Detailed Description ofthe Invention Proliferation, differentiation and death of Cukaryotic cells are controlled by a variety of extracellular signals, such as hormones, neurotransmitters, and polypeptide WO 98!13513 PCT/US97/17159 factors. These diffusible ligands allow cells to influence and be influenced by environmental cues. The study of receptor-ligand interaction has revealed a great deal of information about how cells respond to external stimuli, and this knowledge has led to the development of therapeutically important compounds.
The present invention makes available a rapid, effective assay for screening and identifying pharmaceutically effective compounds that specifically interact with and modulate the activity of a cellular receptor or ion channel. The subject assay enables rapid screening of large numbers of compounds (including, for example, polypeptides in an expression library) to identifying compounds which induce or antagonize receptor bioactivity.
In general, the assay is characterized by the use of a mixture of cells to sample a battery of compounds for receptor/channel agonists or antagonists. As described with greater detail below, the reagent cells express a target receptor protein or ion channel capable of transducing a detectable signal in the reagent cell. The receptor/channel protein can be either endogenous or heterologous. In combination with the disclosed detection means, a culture of the instant reagent cells will provide means for detecting agonists or antagonists of receptor function.
In certain embodiments, a test compound is exogenously added, and its ability to modulate the activity of the target receptor or ion channel is scored in the assay. In other embodiments, the cells are engineered to additionally express a test polypeptide which can be assayed for its ability to interact with the receptor or ion channel. In those embodiments, the assay provides a population of cells which express a library peptides which include potential receptor/channel effectors, and those peptides of the library which either agonize or antagonize the receptor or channel function can be selected and identified by sequence.
The assay of the present invention provides a convenient format for discovering drugs which can be useful to modulate cellular function, as well as to understand the pharmacology of compounds that specifically interact with cellular receptors or ion channels. Moreover, the subject assay is particularly amenable to identifying ligands, natural or artificial, for receptors and ion channels.
I. Definitions Before further description of the invention, certain terms employed in the specification, examples and appended claims are, for convenience, collected here.
As used herein, "heterologous DNA" or "heterologous nucleic acid" includes -i l-DNA that does not occur naturally as part of the genome in which it is present or which is found in a location or locations in the genome that differs from that in which it occurs in nature. Heterologous DNA is not naturally occurring in that position or is not endogenous to the cell into which it is introduced, but has been obtained from another cell. Generally, although not necessarily, such DNA encodes proteins that are not normally produced by the cell in which it is expressed. Heterologous DNA can be from the same species, although in preferred embodiments, it is from a different species. In particularly preferred embodiments, it is mammalian, e.g., human. Heterologous DNA
may also be referred to as foreign DNA. Any DNA that one of skill in the art would recognize or consider as heterologous or foreign to the cell in which is expressed is herein encompassed by the term heterologous DNA. Examples of heterologous DNA
include, but are not limited to, DNA that encodes test polypeptides, receptors, reporter genes, transcriptional and translational regulatory sequences, or selectable or traceable marker proteins, such as a protein that confers drug resistance.
The terms "heterologous protein", "recombinant protein", and "exogenous protein" are used interchangeably throughout the specification and refer to a polypeptide which is produced by recombinant DNA techniques, wherein generally, DNA
encoding the polypeptide is inserted into a suitable expression vector which is in turn used to transform a host cell to produce the heterologous protein. That is, the polypeptide is expressed from a heterologous nucleic acid.
As used herein, "recombinant cells" include any cells that have been modified by the introduction of heterologous DNA. Control cells include cells that are substantially identical to the recombinant cells, but do not express one or more of the proteins encoded by the heterologous DNA, e.g., do not include or express the reporter gene construct, heterologous receptor or test polypeptide.
As used herein, "cell surface receptor" refers to molecules that occur on the surface of cells, interact with the extracellular environment, and transmit or transduce the information regarding the environment intracellularly in a manner that may modulate intracellular second messenger activities or transcription of specific promoters, resulting in transcription of specific genes. A "heterologous receptor" is a specific embodiment of a "heterologous protein", wherein the heterologous receptor is encoded by heterologous DNA and, upon expression of this heterologous DNA in a recombinant cell, the heterologous receptor is expressed in the recombinant cell.
As used herein, the term "extracellular signal" is intended to encompass molecules and changes in the environment that are transduced intracellularly via cell surface proteins that interact, directly or indirectly, with the extracellular signal. An extracellular signal or effector molecule includes any compound or substance that in some manner alters the activity of a cell surface protein. Examples of such signals include, but are not limited to, molecules such as acetylcholine, growth factors and hormones, lipids, sugars and nucleotides that bind to cell surface and/or intracellular receptors and ion channels and modulate the activity of such receptors and channels.
The term, "extracellular signal" also includes as yet unidentified substances that modulate the activity of a cellular receptor, and thereby influence intracellular functions.
Such extracellular signals are potential pharmacological agents that may be used to treat specific diseases by modulating the activity of specific cell surface receptors.
The term "signal transduction" is intended to encompass the processing of physical or chemical signals from the extracellular environment through the cell membrane and into the cell, and may occur through one or more of several mechanisms, such as activation/inactivation of enzymes (such as proteases, or other enzymes which may alter phosphorylation patterns or other post-translational modifications), activation of ion channels or intracellular ion stores, effector enzyme activation via guanine nucleotide binding protein intermediates, formation of inositol phosphate, activation or inactivation of adenylyl cyclase, direct activation (or inhibition) of a transcriptional factor and/or activation. A "signaling pathway" refers to the components involved in "signal transduction" of a particular signal into a cell. The term "endogenous signaling pathway" indicates that some or all of the components of the signaling pathway are naturally-occurring components of the cell. An example of such a pathway is the endogenous pheromone system pathway of yeast.
The term "functionally integrated" (as in a receptor that is "functionally integrated into a signaling pathway in a cell" or "functionally integrated into an endogenous yeast signaling pathway") is intended to refer to the ability of the receptor to be expressed at the surface of the cell and the ability of the expressed receptor to bind to modulators (e.g., a ligand of the receptor) and transduce signals into the cell via components of a signaling pathway of the cell. For example, a G protein coupled receptor (GPCR) which is functionally integrated into an endogenous pheromone response pathway of a yeast cell is expressed on the surface of the yeast cell, couples to a G protein of the pheromone response pathway within the yeast cell and transduces a signal in that yeast cell upon binding of a modulator to the receptor.
The term "endogenous gene" is intended to refer to a gene in a cell that is naturally part of the genome of the cell and which, most preferably, is present in its natural location in the genome (as opposed to "heterologous" DNA which has been introduced into the cell). Likewise, the term "endogenous protein" is intended to include proteins of a cell that are encoded by endogenous genes of the cell.
An endogenous gene may comprise the natural regulatory elements of the gene (e.g.,. the native promoter/enhancer elements that naturally regulate expression of the gene) or the endogenous gene can be "operatively linked to" (i.e., functionally coupled to) a "heterologous promoter" (or other heterologous regulatory elements). A
"heterologous promoter" refers to a promoter that does not naturally regulate the gene to which the heterologous promoter is operatively linked. For example, an endogenous yeast gene that is not normally pheromone-responsive can be operatively linked to a heterologous promoter that is responsive to signals produced by the yeast pheromone system to thereby confer pheromone responsiveness on the endogenous yeast gene (described in further detail below).
The term "detecting an alteration in a signal produced by an endogenous signaling pathway" (e.g., an endogenous yeast signaling pathway) is intended to encompass the detection of alterations in endogenous second messengers produced upon activation of components of the endogenous signaling pathway, alterations in endogenous gene transcription induced upon activation of components of the endogenous signaling pathway, and/or alterations in the activity of an endogenous proteins) upon activation of components of the endogenous signaling pathway.
The terns "detecting an alteration in a signal produced by an endogenous signaling pathway is not, however, intended to encompass detecting alterations in the level of expression of an exogenous reporter gene that has been introduced into the cell or the activity of the reporter gene product. Moreover, the term "detecting an alteration in a signal produced by an endogenous signaling pathway" is not intended to encompass assaying general, global changes to the cell such as changes in cell growth or cell morphology.
Rather, this term indicates that a specific signal associated with the endogenous signaling pathway is assayed.
The term "modulation", as in "modulation of a (heterologous) receptor" and "modulation of a signal transduction activity of a receptor protein" is intended to encompass, in its various grammatical forms, induction and/or potentiation, as well as inhibition and/or downregulation of receptor activity and/or one or more signal transduction pathways downstream of a receptor.
The term "compound" as used herein (e.g., as in "test compound") is meant to include both exogenously added test compounds and peptides endogenously expressed from a peptide library. For example, in certain embodiments, the reagent cell also produces the test compound which is being screened. For instance, the reagent cell can produce. e.g., a test polypeptide, a test nucleic acid and/or a test carbohydrate which is screened for its ability to modulate the receptor/channel activity. In such embodiments, a culture of such reagent cells will collectively provide a library of potential effector molecules and those members of the library which either agonize or antagonize the receptor or ion channel function can be selected and identified. Moreover, it will be apparent that the reagent cell can be used to detect agents which transduce a signal via the receptor or channel of interest.
In other embodiments, the test compound is exogenously added. In such embodiments the test compound is contacted with the reagent cell. Exemplary compounds which can be screened for activity include, but are not limited to, peptides, nucleic acids, carbohydrates, small organic molecules, and natural product extract libraries. In such embodiments, both compounds which agonize or antagonize the receptor- or channel-mediated signaling function can be selected and identified.
The term "non-peptidic compound" is intended to encompass compounds that are comprised, at least in part, of molecular structures different from naturally-occurring L-amino acid residues linked by natural peptide bonds. However, "non-peptidic compounds" are intended to include compounds composed, in whole or in part, of peptidomimetic structures, such as D-amino acids, non-naturally-occurring L-amino acids, modified peptide backbones and the like, as well as compounds that are composed, in whole or in part, of molecular structures unrelated to naturally-occurring L-amino acid residues linked by natural peptide bonds. "Non-peptidic compounds" also are intended to include natural products.
The term "chimeric nucleic acid construct" is intended to refer to a nucleic acid molecule, preferably DNA, composed of at least two discrete segments, a first segment derived from a first gene and a second segment derived from a second gene. The term "derived from" is intended to indicate that the first and second segments have the same or a substantially homologous nucleotide sequence as all or a part of the first and second genes, respectively. Each of the first and second segments encodes a functional polypeptide and are operatively linked such that upon expression of the construct, a fusion protein is produced, the fusion protein comprising a first polypeptide encoded by the first segment and a second polypeptide encoded by the second segment. In a preferred embodiment, the first segment of the chimeric construct encodes a yeast transcription factor that is responsive to signals transduced via the pheromone system pathway and the second segment encodes a DNA binding protein that binds to a DNA
sequence in the regulatory region of an endogenous gene of interest.
A "chimeric substrate" (as in a "chimeric substrate of a BAR1 enzyme) is intended to refer to a substrate composed of two distinct polypeptides, linked to each other, wherein at least one of the polypeptides is cleavable by BAR1.
Preferably the first polypeptide of the chimeric substrates exposes an N-terminal lysine residue upon cleavage by BARI and the second polypeptide is linked to the C-terminus of the first polypeptide. In a preferred embodiment, the first polypeptide is a yeast a-factor polypeptide.
The term "pheromone system protein surrogate" (abbreviated as "PSP
surrogate") is intended to refer to a heterologous protein in a yeast cell which is functionally homologous to a yeast protein of the pheromone system pathway (i.e.,. the PSP surrogate is functionally integrated into the yeast pheromone system pathway).
Examples of PSP surrogates, and methods of preparing yeast cells comprising such PSP
surrogates are described in detail in PCT Publication WO 94/23025. Preferred PSP
surrogates include G protein-coupled receptors, G proteins, proteases, kinases, farnesyltransferases, carboxymethyltransferases, ABC transporters and cyclins.
The term "receptor effector" is intended to include agonists and antagonists that modulate signal transduction via a receptor. Receptor effector molecules are capable of binding to the receptor, though not necessarily at the binding site of the natural ligand.
Receptor effectors can modulate signal transduction when used alone, i.e. can be surrogate ligands, or can alter signal transduction in the presence of the natural ligand, either to enhance or inhibit signaling by the natural ligand. For example, "antagonists"
are molecules that block or decrease the signal transduction activity of receptor, e.g., they can competitively, noncompetitively, and/or allosterically inhibit signal transduction from the receptor, whereas "agonists" potentiate, induce or otherwise enhance the signal transduction activity of a receptor. The terms "receptor activator"
and "surrogate ligand" refer to an agonist which induces signal transduction from a receptor.
"Orphan receptors" is a designation given to a receptors for which no specific natural ligand has been described and/or for which no function has been determined.
The term "indicator gene" generically refers to an expressible (e.g., able to transcribed and (optionally) translated) DNA sequence which is expressed in response to a signal transduction pathway modulated by a target receptor or ion channel.
Exemplary indicator genes include unmodified endogenous genes of the host cell, modified endogenous genes, or a reporter gene of a heterologous construct, e.g., as part of a reporter gene construct.
As used herein, a "reporter gene construct" is a nucleic acid that includes a "reporter gene" operatively linked to at least one transcriptional regulatory sequence.
Transcription of the reporter gene is controlled by these sequences to which they are linked. The activity of at least one or more of these control sequences is directly or indirectly regulated by the target receptor protein. Exemplary transcriptional control sequences are promoter sequences. A reporter gene is meant to include a promoter-reporter gene construct which is heterologously expressed in a cell.
The term "substantially homologous", when used in connection with amino acid sequences, refers to sequences which are substantially identical to or similar in sequence, giving rise to a homology in conformation and thus to similar biological activity. The term is not intended to imply a common evolution of the sequences.
Typically, "substantially homologous" sequences are at least 50%, more preferably at least 80%, identical in sequence, at least over any regions known to be involved in the desired activity. Most preferably, no more than five residues, other than at the termini, are different. Preferably, the divergence in sequence, at least in the aforementioned regions, is in the form of "conservative modifications".
The term "autocrine cell", as used herein, refers to a cell which produces a substance which can stimulate a receptor located on or within the same cell as that which produces the substance. For example, wild-type yeast MATa and MATa cells are not autocrine. However, a yeast cell which produces both a-factor and a-factor receptor, or both a-factor and a-factor receptor, in functional form, is autocrine. By extension, cells which produce a peptide which is being screened for the ability to activate a receptor (e.g., by activating a G protein-coupled receptor) and also express the receptor are called "autocrine cells". In some instances, such cells can also be referred to as "putative autocrine cells" since some of the cells will express peptides from the library which will not activate the receptor which is expressed. In a library of such cells, in which a multitude of different peptides are produced, it is likely that one or more of the cells will be "autocrine" in the stricter sense of the term.
II. General Overview of Assay As set out above, the present invention relates to methods for identifying effectors of a receptor protein or complex thereof. In general, the assay is characterized by the use of a test cell which includes a target receptor or ion channel protein whose signal transduction activity can be modulated by interaction with an extracellular signal, the transduction activity being able to generate a detectable signal. In preferred embodiments, the cell also includes a detection means, such as a reporter gene or an indicator gene, for detecting signals produced by the receptor. In the most preferred embodiments of the invention, an alteration in a signal produced by an endogenous signaling pathway of the cell is detected.
The ability of particular compounds to modulate a signal transduction activity of target receptor or channel can be scored for by detecting up or down-regulation of an endogenous detection signal. For example, second messenger generation (e.g.
GTPase activity, phospholipid hydrolysis, or protein phosphorylation patterns as examples) can be measured directly. In other embodiments, transcription of an endogenous gene or activity of an endogenous protein is used as a detectabel readout.
Alternatively, the use of an indicator gene can provide a convenient readout.
In other embodiments a detection means consists of a reporter gene. In any event, a statistically significant change in the detection signal can be used to facilitate identification of compounds which modulate receptor or ion channel activities.
By this method, compounds which induce a signal pathway from a particular receptor or channel can be identified. If a test compound does not appear to induce the activity of the receptor/channel protein, the assay may be repeated and modified by the introduction of a step in which the reagent cell is first contacted with a known activator of the target receptor/channel to induce signal transduction, and the test compound can be assayed for its ability to inhibit the activated receptor/channel, e.g., to identify antagonists. In yet other embodiments, batteries of compounds can be screened for agents which potentiate the response to a known activator of the receptor.
In developing the subject assays, it was recognized that a frequent result of receptor-mediated responses to extracellular signals was the transcriptional activation or inactivation of specific genes after exposure of the cognate receptor to an extracellular signal that induces such activity. Thus, transcription of genes controlled by receptor-responsive transcriptional elements often reflects the activity of the surface protein by virtue of transduction of an intracellular signal. To illustrate, the intracellular signal that is transduced can be initiated by the specific interaction of an extracellular signal, particularly a ligand, with a cell surface receptor on the cell. This interaction sets in motion a cascade of intracellular events, the ultimate consequence of which is a rapid and detectable change in the transcription or translation of a gene. By selecting transcriptional regulatory sequences that are responsive to the transduced intracellular signals and operatively linking the selected promoters to indicator genes, whose transcription or translation is readily detectable and measurable, a transcription based assay provides a rapid indication of whether a specific receptor or ion channel interacts with a test compound in any way that modulates intracellular transduction.
Expression of the indicator gene, thus, provides a valuable screening tool for the development of compounds that act as agonists or antagonists of a cell receptor or ion channel.

Indicator or reporter gene based assays of this invention measure the end stage of the above described cascade of events, e.g., transcriptionaI modulation.
Accordingly, in practicing one embodiment of the assay, a reporter gene construct is inserted into the reagent cell in order to generate a detection signal dependent on receptor signaling.
Typically, the reporter gene construct will include a reporter gene in operative linkage with one or more transcriptional regulatory elements responsive to the signal transduction activity of the target receptor, with the level of expression of the reporter gene providing the receptor-dependent detection signal. As described below, certain endogenous genes can provide a detectable signal in response to a signal transduetion from a receptor or ion channel, i.e., act as indicator genes. In either embodiment, the amount of transcription from the indicator gene may be measured using any method known to those of skill in the art to be suitable. For example, specific mRNA
expression may be detected using Northern blots or specific protein product may be identified by a characteristic stain or an intrinsic activity.
In preferred embodiments, the gene product of the indicator or reporter gene is detected by an intrinsic activity associated with that product. For instance, the indicator gene may encode a gene product that, e.g., by enzymatic activity, gives rise to a detection signal based on, for example, color, fluorescence, or luminescence.
The amount of expression from the indicator gene is then compared to the amount of expression in either the same cell in the absence of the test compound or it may be compared with the amount of transcription in a substantially identical cell that lacks the specific receptors. A control cell may be derived from the same cells from which the test cell was prepared but which had not been treated with the compound.
Alternatively, it may be a cell in which the receptor of interest are removed.
Any statistically or otherwise significant difference in the amount of transcription indicates that the test compound has in some manner altered the activity of the specific receptor or ion channel.
In other preferred embodiments, the indicator gene provides a selection method such that cells in which activation (or inactivation) of one or more signal pathways of a receptor or ion channel provides a growth advantage to the treated cell. For example, expression of the indicator gene could enhance cell viability, relieve a cell nutritional requirement, and/or provide resistance to a drug.
In other embodiments, changes in intracellular second messenger pathways can be detected biochemically rather than biologically. For example, changes in intracellular Ca+2, phophorylation states of proteins, activities of intracellular enzymes, and the like can be detected. Still other detection techniques include micorphysiometric devices which permit detection of small changes in, e.g., ions or intracellular pH.
With respect to the receptor or ion channel, it may be endogenously expressed by the host cell, or it may be expressed from a heterologous gene that has been introduced into the cell. Methods for introducing heterologous DNA into eukaryotic cells are well known in the art and any such method may be used. In addition, DNA encoding various receptor proteins is known to those of skill in the art or it may be cloned by any method known to those of skill in the art. In certain embodiments, such as when an exogenous receptor is expressed, it may be desirable to inactivate, such as by deletion, a homologous receptor present in the cell.
The subject assay is useful for identifying compounds that interact with any receptor protein whose activity ultimately induces a signal transduction cascade in the host cell which can be exploited to produce a detectable signal. In particular, the assays can be used to test functional ligand-receptor or ligand-ion channel interactions for cell surface-localized receptors and channels, and also for cytoplasmic and nuclear receptors.
As described in more detail below, the subject assay can be used to identify effectors of, for example, G protein-coupled receptors, receptor tyrosine kinases, cytokine receptors, and ion channels, as well as steroid hormone, or other nuclear receptors. In certain embodiments the method described herein is used for identifying ligands for "orphan receptors" for which no ligand is known.
In embodiments utilizing an "autocrine cell" of the present invention, and in which cell surface receptors are the assay targets, it will be desirable for each of the peptides of the peptide library to include a signal sequence for secretion. In certain embodiments the expression of such a signal sequence may ensure appropriate transport of the peptide to the endoplasmic reticulum, the golgi, and ultimately to the cell surface.
When a yeast cell is the host cell, in certain embodiments, the signal sequence will transport peptides to the periplasmic space, however, such transport may not be necessary to achieve autocrine stimulation. .
Any transfectable cell that can express the desired cell surface protein in a manner such the protein functions to intracellularly transduce an extracellular signal may be used. Similarly, any cell surface protein that is known to those of skill in the art or that may be identified by those of skill in the art may used in the assay.
The cell surface protein may endogenously expressed on the selected cell or it may be expressed from cloned DNA.

III. Host Cells Suitable host cells for generating the subject assay include prokaryotes, yeast, or higher eukaryotic cells, including plant and animal cells, especially mammalian cells.
Prokaryotes include gram negative or gram positive organisms. Examples of suitable mammalian host cell lines include the COS-7 line of monkey kidney cells (ATCC
CRL
1651) (Gluzman (1981) Cell 23:175) CV-1 cells (ATCC CCL 70), L cells, C127, 3T3, Chinese hamster ovary (CHO), HeLa, HEK-293, SWISS 3T3, and BHK cell lines.
1f yeast cells are used, the yeast may be of any species which are cultivable and in which an exogenous receptor can be made to engage the appropriate signal transduction machinery of the host cell. Suitable species include Kluyverei lactis, Schizosaccharomyces pombe, and Ustilaqo maydis; Saccharomyces cerevisiae is preferred. Other yeast which can be used in practicing the present invention are Neurospora crassa, Aspergillus niger, Aspergillus nidulans, Pichia pastoris, C'andida tropicalis, and Hansenula polymorpha. The term "yeast", as used herein, includes not only yeast in a strictly taxonomic sense, i.e., unicellular organisms, but also yeast-like multicellular fungi or filamentous fungi.
The choice of appropriate host cell will also be influenced by the choice of detection signal. For instance, reporter constructs, as described below, can provide a selectable or screenable trait upon transcriptional activation (or inactivation) in response to a signal transduction pathway coupled to the target receptor. The reporter gene may be an unmodified gene already in the host cell pathway, such as the genes responsible for growth arrest in yeast. It may be a host cell gene that has been operably linked to a "receptor-responsive" promoter. Alternatively, it may be a heterologous gene (e.g., a "reporter gene construct") that has been so linked. Suitable genes and promoters are discussed below. In other embodiments, second messenger generation can be measured directly in the detection step, such as mobilization of intracellular calcium or phospholipid metabolism are quantitated. In yet other embodiments indicator genes can be used to detect receptor-mediated signaling.
Accordingly, it will be understood that to achieve selection or screening, the host cell must have an appropriate phenotype. For example, generating a pheromone-responsive chimeric HIS3 gene in a yeast that has a wild-type HIS3 gene would frustrate genetic selection. Thus, to achieve nutritional selection, an auxotrophic strain is preferred.
A variety of complementations for use in the subject assay can be constructed.
Indeed, many yeast genetic complementation with mammalian signal transduction proteins have been described in the art. For example, Mosteller et aI. ( 1994) Mol Cell Biol 14:1104-12 demonstrates that human Ras proteins can complement loss of ras mutations in S. cerevisiae. Moreover, Toda et al. ( 1986) Princess Takamatsu Symp 17:
253-60 have shown that human ras proteins can complement the loss of RAS I and RAS2 proteins in yeast, and hence are functionally homologous. Both human and yeast RAS proteins can stimulate the magnesium and guanine nucleotide-dependent adenylate cyclase activity present in yeast membranes. Ballester et al. (1989) Cell 59:

describe a vector to express the mammalian GAP protein in the yeast S.
cerevisiae.
When expressed in yeast, GAP inhibits the function of the human ras protein, and complements the loss of IRA1. IRA/ is a yeast gene that encodes a protein with homology to GAP and acts upstream of RAS. Mammalian GAP can therefore function in yeast and interact with yeast RAS. Wei et al. (1994) Gene 151: 279-84 describes that a human Ras-specific guanine nucleotide-exchange factor, Cdc25GEF, can complement the loss of CDC25 function in S. cerevisiae. Martegani et al. (1992) EMBO J
11: 2151-7 describe the cloning by functional complementation of a mouse cDNA encoding a homolog of CDC25, a Saccharomyces cerevisiae RAS activator. Vojtek et al.
(1993) J
Cell Sci 105: 777-85 and Matviw et al. (1992) Mol Cell Biol 12: 5033-40 describe how a mouse CAP protein, e.g., an adenylyl cyclase associated protein associated with ras-mediated signal transduction, can complements defects in S. cerevisiae.
Papasavvas et al. (1992) Biochem Biophys Res Commun 184:1378-85 also suggest that inactivated yeast adenyl cyclase can be complemented by a mammalian adenyl cyclase gene.
Hughes et al. (1993) Nature 364: 349-52 describe the complementation of byrl in fission yeast by mammalian MAP kinase kinase (MEK). Parissenti et al. (1993) Mol Cell Endocrinol 98: 9-16 describes the reconstitution of bovine protein kinase C (PKC) in yeast. The Ca(2+)- and phospholipid-dependent Ser/Thr kinase PKC plays important roles in the transduction of cellular signals in mammalian cells. Marcus et al. (1995) PNAS 92: 6180-4 suggests the complementation of shkl null mutations in S.
pombe by the either the structurally related S. cerevisiae Ste20 or mammalian p65PAK
protein kinases.
"Inactivation", with respect to genes of the host cell, means that production of a functional gene product is prevented or inhibited. Inactivation may be achieved by deletion of the gene, mutation of the promoter so that expression does not occur, or mutation of the coding sequence so that the gene product is inactive.
Inactivation may be partial or total.
"Complementation", with respect to genes of the host cell, means that at least partial function of inactivated gene of the host cell is supplied by an exogenous nucleic acid. For instance, yeast cells can be "mammalianized", and even "humanized", by complementation of receptor and signal transduction proteins with mammalian homologs. To illustrate, inactivation of a yeast Byr2/Stel 1 gene can be complemented by expression of a human MEKK gene.
IV. Expression Systems Ligating a polynucleotide coding sequence into a gene construct, such as an expression vector, and transforming or transfecting into hosts, either eukaryotic (yeast, avian, insect or mammalian) or prokaryotic (bacterial cells), are standard procedures used in producing other well-known proteins, including sequences encoding exogenous receptor and peptide libraries. Similar procedures, or modifications thereof, can be employed to prepare recombinant reagent cells of the present invention by tissue-culture technology in accord with the subject invention.
In general, it will be desirable that the vector be capable of replication in the host cell. It may be a DNA which is integrated into the host genome, and thereafter is replicated as a part of the chromosomal DNA, or it may be DNA which replicates autonomously, as in the case of a plasmid. In the latter case, the vector will include an origin of replication which is functional in the host. In the case of an integrating vector, the vector may include sequences which facilitate integration, e.g., sequences homologous to host sequences, or encoding integrases.
Appropriate cloning and expression vectors for use with bacterial, fungal, yeast, and mammalian cellular hosts are known in the art, and are described in, for example, Powels et al. (Cloning Vectors: A Laboratory Manual, Elsevier, New York, 1985).
Mammalian expression vectors may comprise non-transcribed elements such as an origin of replication, a suitable promoter and enhancer linked to the gene to be expressed, and other 5' or 3' flanking nontranscribed sequences, and 5' or 3' nontranslated sequences, such as necessary ribosome binding sites, a poly-adenyIation site, splice donor and acceptor sites, and transcriptional termination sequences.
Preferred mammalian expression vectors contain both prokaryotic sequences, to facilitate the propagation of the vector in bacteria, and one or more eukaryotic transcription units that are expressed in eukaryotic cells. The pcDNAI/amp, pcDNAI/neo, pRc/CMV, pSV2gpt, pSV2neo, pSV2-dhfr, pTk2, pRSVneo, pMSG, pSVT7, pko-neo and pHyg derived vectors are examples of mammalian expression vectors suitable for transfection of eukaryotic cells. Some of these vectors are modified with sequences from bacterial plasmids, such as pBR322, to facilitate replication and drug resistance selection in both prokaryotic and eukaryotic cells.
Alternatively, derivatives of viruses such as the bovine papillomavirus (BPV-1 ), or Epstein-Barr virus (pHEBo, pREP-derived and p205) can be used for transient expression of proteins in eukaryotic cells. The various methods employed in the preparation of the plasmids and transformation of host organisms are well known in the art. For other suitable expression systems for both prokaryotic and eukaryotic cells, as well as general recombinant procedures, see Molecular Cloning A Laboratory Manual, 2nd Ed., ed. by Sambrook, Fritsch and Maniatis (Cold Spring Harbor Laboratory Press: 1989) Chapters 16 and 17.
Transcriptional and translational control sequences in expression vectors to be used in transforming mammalian cells may be provided by viral sources. For example, commonly used promoters and enhancers are derived from Polyoma, Adenovirus 2, Simian Virus 40 (SV40), and human cytomegalovirus. DNA sequences derived from the SV40 viral genome, for example, SV40 origin, early aiZd late promoter, enhancer, splice, and polyadenylation sites may be used to provide the other genetic elements required for expression of a heterologous DNA sequence. The early and late promoters are particularly useful because both are obtained easily from the virus as a fragment which also contains the SV40 viral origin of replication (Fiers et a1.(1978) Nature 273:1 I I ) Smaller or larger SV40 fragments may also be used, provided the approximately 250 by sequence extending from the Hind III site toward the Bgl I site located in the viral origin of replication is included. Exemplary vectors can be constructed as disclosed by Okayama and Berg (1983, Mol. Cell Biol. 3:280). A
useful system for stable high level expression of mammalian receptor cDNAs in CI27 murine mammary epithelial cells can be constructed substantially as described by Cosman et al (1986, Alol. Immunol. 23:930. Other expression vectors for use in mammalian host cells are derived from retroviruses.
In other embodiments, the use of viral transfection can provide stably integrated copies of the expression construct. In particular, the use of retroviral, adenoviral or adeno-associated viral vectors is contemplated as a means for providing a stably transfected cell line which expresses an exogenous receptor, and/or a polypeptide library.
A number of vectors exist for the expression of recombinant proteins in yeast.
For instance, YEP24, YIPS, YEP51, YEP52, pYES2, and YRP17 are cloning and expression vehicles useful in the introduction of genetic constructs into S.
cerevi,riae (see, for example, Broach et al. (1983) in Experimental tLlanipulation of Gene Expression, ed. M. Inouye Academic Press, p. 83).
These vectors can replicate in E. coli due the presence of the pBR322 ori, and in S.
cerevisiae due to the replication determinant of the yeast 2 micron plasmid.
In addition, drug resistance markers such as ampicillin can be used. Moreover, if yeast are used as a host cell, it will be understood that the expression of a gene in a yeast cell requires a promoter which is functional in yeast. Suitable promoters include the promoters for metallothionein, 3-phosphoglycerate kinase (Hitzeman et al., J. Biol. Chem.
255, 20?3 ( 1980) or other glycolytic enzymes (Hess et al., J. Adv. Enzyme Req. 7, 149 ( 1968); and Holland et al. Biochemistry 17, 4900 ( 1978)), such as enolase, glyceraldehyde-3-phosphate dehydrogenase, hexokinase, pyruvate decarboxylase, phospho-fructokinase, glucose-6-phosphate isomerase, 3-phosphoglycerate mutase, pyruvate kinase, triosephosphate isomerase, phospho-glucose isomerase, and glucokinase.
Suitable vectors and promoters for use in yeast expression are further described in R.
Hitzeman et al., European patent No. 73,657B 1 published on 2-7 December 1990.
Other promoters, which have the additional advantage of transcription controlled by growth conditions, are the promoter regions for alcohol dehydrogenase 2, isocytochrome C, acid phosphatase, degradative enzymes associated with nitrogen metabolism, and the aforementioned metallothionein and glyceraldehyde-3-phosphate dehydrogenase, as well as enzymes responsible for maltose and galactose utilization. Finally, promoters that are active in only one of the two haploid mating types may be appropriate in certain circumstances. Among these haploid-specific promoters, the pheromone promoters MFaI
and MFaI are of particular interest.
In some instances, it may be desirable to use insect cells ase the host cells.
In such embodiments, recombinant polypeptides can be expressed by the use of a baculovirus expression system. Examples of such baculovirus expression systems include pVL-derived vectors (such as pVL1392, pVL1393 and pVL941), pAeUW-derived vectors (such as pAcUW1), and pl3lueBac-derived vectors (such as the (3-gal containing pBlueBac'III).
In constructing suitable expression plasmids, the termination sequences associated with these genes, or with other genes which are efficiently expressed in yeast, may also be ligated into the expression vector 3' of the heterologous coding sequences to provide polyadenylation and termination of the mRNA.
I! Periulasmic Secretion In embodiments in which yeast cells are used as the host cell and the compounds tested are endogenously expressed from a library, it will be noted that the yeast cell is bounded by a lipid bilayer called the plasma membrane. Between this plasma membrane and the cell wall is the periplasmic space. Peptides secreted by yeast cells cross the plasma membrane through a variety of mechanisms and thereby enter the periplasmic * Trade-mark space. The secreted peptides are then free to interact with other molecules that are present in the periplasm or displayed on the outer surface of the plasma membrane. The peptides then either undergo re-uptake into the cell, diffuse through the cell wall into the medium, or become degraded within the periplasmic space.
The test polypeptide library may be secreted into the periplasm by any of a number of exemplary mechanisms, depending on the nature of the expression system to which they are linked. In one embodiment, the peptide may be structurally linked to a yeast signal sequence, such as that present in the a-factor precursor, which directs secretion through the endoplasmic reticulum and Golgi apparatus. Since this is the same route that the receptor protein follows in its journey to the plasma membrane, opportunity exists in cells expressing both the receptor and the peptide library for a specific peptide to interact with the receptor during transit through the secretory pathway. This has been postulated to occur in mammalian cells exhibiting autocrine activation. Such interaction could yield activation of the response pathway during transit, which would still allow identification of those cells expressing a peptide agonist.
For situations in which peptide antagonists to externally applied receptor agonist are sought, this system would still be effective, since both the peptide antagonist and receptor would be delivered to the outside of the cell in concert. Thus, those cells producing an antagonist would be selectable, since the peptide antagonist would be properly and timely situated to prevent the receptor from being stimulated by the externally applied agonist.
An alternative mechanism for delivering peptides to the periplasmic space is to use the ATP-dependent transporters of the STE6/MDRl class. This transport pathway and the signals that direct a protein or peptide to this pathway are not as well characterized as is the endoplasmic reticulum-based secretory pathway.
Nonetheless, these transporters apparently can efficiently export certain peptides directly across the plasma membrane, without the peptides having to transit the ER/Golgi pathway.
It is anticipated that at least a subset of peptides can be secreted through this pathway by expressing the library in context of the a-factor prosequence and terminal tetrapeptide.
The possible advantage of this system is that the receptor and peptide do not come into contact until both are delivered to the external surface of the cell. Thus, this system strictly mimics the situation of an agonist or antagonist that is normally delivered from outside the cell. Use of either of the described pathways is within the scope of the invention.
The present invention does not require periplasmic secretion, or, if such secretion is provided, any particular secretion signal or transport pathway.

VI. Receptors Cytokine Receptors In one embodiment the target receptor is a cytokine receptor. Cytokines are a family of soluble mediators of cell-to-cell communication that includes interleukins, interferons, and colony-stimulating factors. The characteristic features of cytokines lie in their functional redundancy and pleiotropy. Most of the cytokine receptors that constitute distinct superfamilies do not possess intrinsic protein tyrosine kinase domains, yet receptor stimulation usually invokes rapid tyrosine phosphorylation of intracellular proteins, including the receptors themselves. Many members of the cytokine receptor superfamily acitvate the Jak protein tyrosine kinase family, with resultant phosphorylation of the STAT transcriptional activator factors. IL-2, IL-7, IL-2 and Interferon y have all been shown to activate Jak kinases (Frank et al (1995) Proc Natl Acad Sci USA 92:7779-7783); Scharfe et al. (1995) Blood 86:2077-2085); (Bacon et al.
(1995) Proc Natl Acad Sci USA 92:7307-7311); and (Sakatsume et al (1995) J.
Biol Chem 270:17528-17534). Events downstream of Jak phosphorylation have also been elucidated. For example, exposure of T lymphocytes to IL-2 has been shown to lead to the phosphorylation of signal transducers and activators of transcription (STAT) proteins STATIa, STAT2(3, and STAT3, as well as of two STAT-related proteins, p94 and p95. The STAT proteins were found to translocate to the nucleus and to bind to a specific DNA sequence, thus suggesting a mechanism by which IL-2 may activate specific genes involved in immune cell function (Frank et al. supra). Jak3 is associated with the gamma chain of the IL-2, IL-4, and IL-7 cytokine receptors (Fujii et al. (1995) Proc Natl Acad ,Sci 92:5482-5486) and (Musso et al (1995) J Exp Med. 181:1425-1431 ). The Jak kinases have also been shown to be activated by numerous ligands that signal via cytokine receptors such as, growth hormone and erythropoietin and (Kishimoto {1994) Stem cells Suppl 12:37-44).
Signal transduction which may be detected in the instant assays, in addition to direct detection of second messengers, (e.g., by measuring changes in phosphorylation) includes reporter constructs or indicator genes which include transcriptionaI
regulatory elements responsive to the STAT proteins. Described infra.
Multisubunit Immune Recognition Receptor (MIRR).
In another embodiment the receptor is a multisubunit receptor. Receptors can be comprised of multiple proteins referred to as subunits, one category of which is referred to as a multisubunit receptor is a multisubunit immune recognition receptor (MIRR).
MIRRs include receptors having multiple noncovalently associated subunits and are capable of interacting with src-family tyrosine kinases. MIRRs can include, but are not limited to, B cell antigen receptors, T cell antigen receptors, Fc receptors and CD22.
One example of an MIRR is an antigen receptor on the surface of a B cell. To further illustrate, the MIRR on the surface of a B cell comprises membrane-bound immunoglobulin (mIg) associated with the subunits Ig-a and Ig-~i or Ig-y, which forms a complex capable of regulating B cell function when bound by antigen. An antigen receptor can be functionally linked to an amplifier molecule in a manner such that the amplifier molecule is capable of regulating gene transcription.
Src-family tyrosine kinases are enzymes capable of phosphorylating tyrosine residues of a target molecule. Typically, a src-family tyrosine kinase contains one or more binding domains and a kinase domain. A binding domain of a src-family tyrosine kinase is capable of binding to a target molecule and a kinase domain is capable of phosphorylating a target molecule bound to the kinase. Members of the src family of tyrosine kinases are characterized by an N-terminal unique region followed by three regions that contain different degrees of homology among all the members of the family.
These three regions are referred to as src homology region 1 (SH1), src homology region 2 (SH2) and src homology region 3 (SH3). Both the SH2 and SH3 domains are believed to have protein association functions important for the formation of signal transduction complexes. The amino acid sequence of an N-terminal unique region, varies between each src-family tyrosine kinase. An N-terminal unique region can be at least about the first 40 amino acid residues of the N-terminal of a src-family tyrosine kinase.
Syk-family kinases are enzymes capable of phosphorylating tyrosine residues of a target molecule. Typically, a syk-family kinase contains one or more binding domains and a kinase domain. A binding domain of a syk-family tyrosine kinase is capable of binding to a target molecule and a kinase domain is capable of phosphorylating a target molecule bound to the kinase. Members of the syk- family of tyrosine kinases are characterized by two SH2 domains for protein association function and a tyrosine kinase domain.
A primary target molecule is capable of further extending a signal transduction pathway by modifying a second messenger molecule. Primary target molecules can include, but are not limited to, phosphatidylinositol 3-kinase (PI-3K), P2lrasGAPase-activating protein and associated P190 and P62 protein, phospholipases such as PLCyl and PLCy2, MAP kinase, Shc and VAV. A primary target molecule is capable of producing second messenger molecule which is capable of further amplifying a transduced signal. Second messenger molecules include, but are not limited to diacylglycerol and inositol 1,4,5-triphosphate (IP3). Second messenger molecules are capable of initiating physiological events which can lead to alterations in gene transcription. For example, production of IP3 can result in release of intracellular calcium, which can then lead to activation of calmodulin kinase II, which can then lead to serine phosphorylation of a DNA binding protein referred to as ets-1 proto-onco-protein. Diacylglycerol is capable of activating the signal transduction protein, protein kinase C which affects the activity of the AP 1 DNA binding protein complex.
Signal transduction pathways can lead to transcriptional activation of genes such as c-fos, egr-1, and c-myc.
Shc can be thought of as an adapter molecule. An adapter molecule comprises a protein that enables two other proteins to form a complex (e.g., a three molecule complex). Shc protein enables a complex to form which includes Grb2 and SOS.
Shc comprises an SH2 domain that is capable of associating with the SH2 domain of Grb2.
Molecules of a signal transduction pathway can associate with one another using recognition sequences. Recognition sequences enable specific binding between two molecules. Recognition sequences can vary depending upon the structure of the molecules that are associating with one another. A molecule can have one or more recognition sequences, and as such can associate with one or more different molecules.
Signal transduction pathways for MIRR complexes are capable of regulating the biological functions of a cell. Such functions can include, but are not limited to the ability of a cell to grow, to differentiate and to secrete cellular products.
MIRR-induced signal transduction pathways can regulate the biological functions of specific types of cells involved in particular responses by an animal, such as immune responses, inflammatory responses and allergic responses. Cells involved in an immune response can include, for example, B cells, T cells, macrophages, dendritic cells, natural killer cells and plasma cells. Cells involved in inflammatory responses can include, for example, basophils, mast cells, eosinophils, neutrophils and macrophages.
Cells involved in allergic responses can include, for example mast cells, basophils, B cells, T
cells and macrophages.
In exemplary embodiments of the subject assay, signal transduction is measured by detection of second messengers, such as a phosphorylated src-like protein, includes reporter constructs or indicator genes which include transcriptional regulatory elements such as serum response element (SRE}, 12-O-tetradecanoyl-phorbol-13-acetate response element, cyclic AMP response element, c- fos promoter, or a CREB-responsive element.

Nuclear Receptors.
In another embodiment, the target receptor is a nuclear receptor. The nuclear receptors may be viewed as ligand-dependent transcription factors. These receptors provide a direct link between extracellular signals, mainly hormones, and transcriptional responses. Their transcriptional activation function is regulated by endogenous small molecules, such as steroid hormones, vitamin D, ecdysone, retinoic acids and thyroid hormones, which pass readily through the plasma membrane and bind their receptors inside the cell (Laudet and Adelmant (1995) Current Biology 5:124). The majority of these receptors appear to contain three domains: a variable amino terminal domain; a highly conserved, DNA-binding domain and a moderately conserved, carboxyl-terminal ligand-binding domain (Power et al. (1993) Curr. Opin. Cell Biol. 5:499-504).
Examples include the estrogen, progesterone, androgen, thyroid hormone and mineralocorticoid receptors. In addition to the known steroid receptors, at least 40 orphan members of this superfamily have been identified. (Laudet et al., ( 1992) EMBO
J. 11:1003-1013). There are at least four groups of orphan nuclear receptors represented by NGF1, FTZ-F1, Rev-erbs, and RARs, which are by evolutionary standards, only distantly related to each other (Laudet et al. supra). While the steroid hormone receptors bind exclusively as homodimers to a palindrome of their hormone responsive element other nuclear receptors bind as heterodimers. Interestingly, some orphan receptors bind as monomers to similar response elements and require for their function a specific motif that is rich in basic amino-acid residues and is located corboxy-terminal to the DNA-binding domain (Laudet and Adelmant supra.) In preferred embodiments, the subject assay utilizes a hormone-dependent reporter construct for selection. For instance, glucocorticoid response elements (GREs) and thyroid receptor enhancer-like DNA sequences (TREs) can be used to drive expression of reporter construct in response to hormone binding to hormone receptors.
GRE's are enhancer-like DNA sequences that confer glucocorticoid responsiveness via interaction with the glucocorticoid receptor. See Payvar, et al. (1983) Cell 35:381 and Schiedereit et al. (1983) Nature 304:749. TRE's are similar to GRE's except that they confer thyroid hormone responsiveness via interaction with thyroid hormone receptor. It is known that a steroid or thyroid hormone enters cells by facilitated diffusion and binds to its specific receptor protein, initiating an allosteric alteration of the protein. As a result of this alteration, the hormone/receptor complex is capable of binding to certain specific sites on transcriptional regulatory sequence with high affinity.
Many of the primary effects of steroid and thyroid hormones involve increased transcription of a subset of genes in specific cell types. Moreover, there is evidence that activation of transcription {and, consequently, increased expression) of genes which are responsive to steroid and thyroid hormones (through interaction of chromatin with hormone receptor/hormone complex) is effected through binding of the complex to enhancers associated with the genes.
A number of steroid hormone and thyroid hormone responsive transcriptional control units, some of which have been shown to include enhancers, have been identified. These include the mouse mammary tumor virus 5'-long terminal repeat (MMTV LTR}, responsive to glucocorticoid, aldosterone and androgen hormones;
the transcriptional control units for mammalian growth hormone genes, responsive to glucocorticoids, estrogens, and thyroid hormones; the transcriptional control units for mammalian prolactin genes and progesterone receptor genes, responsive to estrogens;
the transcriptional control units for avian ovalbumin genes, responsive to progesterones;
mammalian metallothionein gene transcriptional control units, responsive to glucocorticoids; and mammalian hepatic alpha 2u -globulin gene transcriptional control units, responsive to androgens, estrogens, thyroid hormones and glucocorticoids. Such steroid hormone and thyroid hormone responsive transcriptional control units can be used to generate reporter constructs or indicator genes which are sensitive to agonists and antagonists of the steroid hormone and/or thyroid hormone receptors. See, for example, U.S. Patents 5,298,429 and 5,071,773, both to Evans, et. al.
Moreover, the art describes the functional expression of such receptors in yeast. See also for example, Caplan et al. (1995) JBiol Chem 270:5251-7; and Baniahmad et al. (1995) Mol Endocrinol 9: 34-43.
Receptor tyrosine kinases.
In still another embodiment, the target receptor is a receptor tyrosine kinase. The receptor tyrosine kinases can be divided into five subgroups on the basis of structural similarities in their extracellular domains and the organization of the tyrosine kinase catalytic region in their cytoplasmic domains. Sub-groups I (epidermal growth factor (EGF) receptor-like), II (insulin receptor-like) and the eph/eck family contain cysteine-rich sequences (Hirai et al., (1987) Science 238:1717-1720 and Lindberg and Hunter, (1990) Mol. Cell. Biol. 10:6316-6324). The functional domains of the kinase region of these three classes of receptor tyrosine kinases are encoded as a contiguous sequence Hanks et al. ( 1988} Science 241:42-52). Subgroups III (platelet-derived growth factor (PDGF} receptor-like) and IV (the fibro-blast growth factor (FGF) receptors) are characterized as having immunoglobulin (Ig)-like folds in their extracellular domains, as well as having their kinase domains divided in two parts by a variable stretch of unrelated amino acids (Yanden and Ullrich (1988) supra and Hanks et al. (1988) supra).
The family with by far the largest number of known members is the EPH family.
Since the description of the prototype, the EPH receptor (Hirai et al. (1987) Science 238:1717-1720), sequences have been reported for at least ten members of this family, not counting apparently orthologous receptors found in more than one species.
Additional partial sequences, and the rate at which new members are still being reported, suggest the family is even larger (Maisonpierre et al. (1993) Oncogene 8:3277-3288;
Andres et al. ( 1994) Oncogene 9:1461-1467; Henkemeyer et a1. ( I 994) Oncogene 9:1001-1014; Ruiz et al. ( I 994) Mech Dev 46:87-100; Xu et al. ( 1994) Development 120:287-299; Zhou et al. (1994).INeurosci Res 37:129-143; and references in Tuzi and Gullick ( I 994) Br J Cancer 69:417-421 ). Remarkably, despite the large number of members in the EPH family, all of these molecules were identified as orphan receptors without known ligands.
The expression patterns determined for some of the EPH family receptors have implied important roles for these molecules in early vertebrate development.
In particular, the timing and pattern of expression of sek, mek=l and some of the other receptors during the phase of gastrulation and early organogenesis has suggested functions for these receptors in the important cellular interactions involved in patterning the embryo at this stage (Gilardi-Hebenstreit et al. ( 1992) Oncogene 7:2499-2506; Nieto et al. (1992) Development 116:1137-1150; Henkemeyer et aL, .supra; Ruiz et al., supra;
and Xu et al., supra). Sek, for example, shows a notable early expression in the two areas of the mouse embryo that show obvious segmentation, namely the somites in the mesoderm and the rhombomeres of the hindbrain; hence the name sek, for segmentally expressed kinase (Gilardi-Hebenstreit et al., supra; Nieto et al., supra). As in Drosophila, these segmental structures of the mammalian embryo are implicated as important elements in establishing the body plan. The observation that Sek expression precedes the appearance of morphological segmentation suggests a role for sek in forming these segmental structures, or in determining segment-specific cell properties such as lineage compartmentation (Nieto et al., supra). Moreover, EPH
receptors have been implicated, by their pattern of expression, in the development and maintenance of nearly every tissue in the embryonic and adult body. For instance, EPH
receptors have been detected throughout the nervous system, the testes, the cartilaginous model of the skeleton, tooth primordia, the infundibular component of the pituitary, various epithelia tissues, lung, pancreas, liver and kidney tissues. Observations such as this have been indicative of important and unique roles for EPH family kinases in development and physiology, but further progress in understanding their action has been severely limited by the lack of information on their ligands.
As used herein, the terms "EPH receptor" or "EPH-type receptor" refer to a class of receptor tyrosine kinases, comprising at least eleven paralogous genes, though many more orthologs exist within this class, e.g. homologs from different species.
EPH
receptors, in general, are a discrete group of receptors related by homology and easily recognizable, e.g., they are typically characterized by an extracellular domain containing a characteristic spacing of cysteine residues near the N-terminus and two fibronectin type III repeats (Hirai et al. ( 1987) Science 238: I 717-1720; Lindberg et al. { 1990) Mol Cell Biol 10:6316-6324; Chan et al. ( I 991 ) Oncogene 6:1057-1061;
Maisonpierre et al.
( 1993 ) Oncogene 8:3277-3288; Andres et al. ( / 994) Oncogene 9:1461-1467;
Henkemeyer et al. ( I 994) Oncogene 9:1001-1014; Ruiz et al. ( 1994) Mech Dev 46:87-100; Xu et al. (1994) Development 120:287-299; Zhou et al. (1994) JNeurosci Res 37: I 29-143; and references in Tuzi and Gullick ( 1994) Br J Cancer 69:417-421 ).
Exemplary EPH receptors include the eph, elk, eck, sek, mek4, hek, hek2, eek, erk, tyrol, tyro, tyros, tyro6, tyroll, cek=l, cek5, cek6, cek7, cek8, cek9, cekl0, bsk, rtkl, rtk2, rtk3, mykl , myk2, ehkl , ehk2, pagliaccio, htk, erk and nuk receptors. The term "EPH
receptor" refers to the membrane form of the receptor protein, as well as soluble extracellular fragments which retain the ability to bind the ligand of the present invention.
In exemplary embodiments, the detection signal is provided by detecting phosphorylation of intracellular proteins, e.g., MEKKs, MEKs, or Map kinases, or by the use of reporter constructs or indicator genes which include transcriptional regulatory elements responsive to c-fos and/or c-jun. Described infra.
G Protein-Coupled Receptors One family of signal transduction cascades found in eukaryotic cells utilizes heterotrimeric "G proteins." Many different G proteins are known to interact with receptors. G protein signaling systems include three components: the receptor itself, a GTP-binding protein (G protein), and an intracellular target protein. The cell membrane acts as a switchboard. Messages arriving through different receptors can produce a single effect if the receptors act on the same type of G protein. On the other hand, signals activating a single receptor can produce more than one effect if the receptor acts on different kinds of G proteins, or if the G proteins can act on different effectors.
In their resting state, the G proteins, which consist of alpha (a), beta ((3) and gamma (y) subunits, are complexed with the nucleotide guanosine diphosphate (GDP) and are in contact with receptors. When a hormone or other first messenger binds to receptor, the receptor changes conformation and this alters its interaction with the G
protein. This spurs the a subunit to release GDP, and the more abundant nucleotide guanosine triphosphate (GTP), replaces it, activating the G protein. The G
protein then dissociates to separate the a subunit from the still complexed beta and gamma subunits.
Either the Ga subunit, or the G~3y complex, depending on the pathway, interacts with an effector. The effector (which is often an enzyme) in turn converts an inactive precursor molecule into an active "second messenger," which may diffuse through the cytoplasm, triggering a metabolic cascade. After a few seconds, the Ga converts the GTP
to GDP, thereby inactivating itself. The inactivated Ga may then reassociate with the G(3y complex.
Hundreds, if not thousands, of receptors convey messages through heterotrimeric G proteins, of which at least 17 distinct forms have been isolated. Although the greatest variability has been seen in the a subunit, several different (3 and y structures have been reported. There are, additionally, several different G protein-dependent effectors.
Most G protein-coupled receptors are comprised of a single protein chain that is threaded through the plasma membrane seven times. Such receptors are often referred to as seven-transmembrane receptors (STRs). More than a hundred different STRs have been found, including many distinct receptors that bind the same ligand, and there are likely many more STRs awaiting discovery.
In addition, STRs have been identified for which the natural ligands are unknown; these receptors are termed "orphan" G protein-coupled receptors, as described above. Examples include receptors cloned by Neote et al. (1993) Cell 72, 415;
Kouba et al. FEBS Lett. (1993) 321, 173; Birkenbach et a1.(1993) J. Virol. 67, 2209.
The "exogenous receptors" of the present invention may be any G
protein-coupled receptor, preferably exogenous to the cell, which is to be genetically engineered for the purpose of the present invention. This receptor may be a plant or animal cell receptor. Screening for binding to plant cell receptors may be useful in the development of, e.g., herbicides. In the case of an animal receptor, it may be of invertebrate or vertebrate origin. If an invertebrate receptor, an insect receptor is preferred, and would facilitate development of insecticides. The receptor may also be a vertebrate, more preferably a mammalian, still more preferably a human, receptor. The exogenous receptor is also preferably a seven transmembrane segment receptor.
Known ligands for G protein coupled receptors include: purines and nucleotides, such as adenosine, cAMP, ATP, UTP, ADP, melatonin and the like; biogenic amines (and related natural ligands), such as 5-hydroxytryptamine, acetylcholine, dopamine, adrenaline, adrenaline, adrenaline., histamine, noradrenaline, noradrenaline, noradrenaline., tyramine/octopamine and other related compounds; peptides such as adrenocorticotrophic hormone (acth), melanocyte stimulating hormone (msh), melanocortins, neurotensin (nt), bombesin and related peptides, endothelins, cholecystokinin, gastrin, neurokinin b (nk3), invertebrate tachykinin-like peptides, substance k (nk2), substance p (nkl), neuropeptide y (npy), thyrotropin releasing-factor (trf), bradykinin, angiotensin ii, beta-endorphin, c5a anaphalatoxin, calcitonin, chemokines (also called intererines), corticotrophic releasing factor (crf), dynorphin, endorphin, fmlp and other formylated peptides, follitropin (fsh), fungal mating pheromones, galanin, gastric inhibitory polypeptide receptor (gip), glucagon-like peptides (glps), glucagon, gonadotropin releasing hormone (gnrh), growth hormone releasing hormone(ghrh), insect diuretic hormone, interleukin-8, leutropin (lh/hcg), met-enkephalin, opioid peptides, oxytocin, parathyroid hormone (pth) and pthrp, pituitary adenylyl cyclase activating peptide (pacap), secretin, somatostatin, thrombin, thyrotropin (tsh), vasoactive intestinal peptide (vip), vasopressin, vasotocin; eicosanoids such as ip-prostacyclin, pg-prostaglandins, tx-thromboxanes; retinal based compounds such as vertebrate 11-cis retinal, invertebrate 11-cis retinal and other related compounds;
lipids and lipid-based compounds such as cannabinoids, anandamide, lysophosphatidic acid, platelet activating factor, leukotrienes and the like; excitatory amino acids and ions such as calcium ions and glutamate.
Examples of G-protein coupled receptors include, but are not limited to, dopaminergic, muscarinic choIinergic, a-adrenergic, b-adrenergic, opioid (including delta and mu), cannabinoid, serotoninergic, and GABAergic receptors. Preferred receptors include the SHT family of receptors, dopamine receptors,CSa receptor and FPRL-I receptor, cyclo-histidyl-proline-diketoplperazine receptors, melanocyte stimulating hormone release inhibiting factor receptor, and receptors for neurotensin, thyrotropin releasing hormone, calcitonin, cholecytokinin-A, neurokinin-2, histamine-3, cannabinoid, melanocortin, or adrenomodulin, neuropeptide-Y 1 or galanin.
Other G
protein coupled receptors (GPCRs) are listed in the art. The term "receptor,"
as used herein, encompasses both naturally occurring and mutant receptors.
Many of these G protein-coupled receptors, like the yeast a- and a-factor receptors, contain seven hydrophobic amino acid-rich regions which are assumed to lie within the plasma membrane. Specific human G protein-coupled STRs for which genes have been isolated and for which expression vectors could be constructed include those listed herein and others known in the art. Thus, the gene would be operably linked to a promoter functional in the cell to be engineered and to a signal sequence that also functions in the cell. For example in the case of yeast, suitable promoters include Ste2, Ste3 and ag 110. Suitable signal sequences include those of Ste2, Ste3 and of other genes which encode proteins secreted by yeast cells. Preferably, when a yeast cell is used, the codons of the gene would be optimized for expression in yeast. See Hoekema et a1.,(1987) Mol. Cell. Biol., 7:2914-24; Sharp, et al., (1986)14:5125-43.
The homology of STRs is discussed in Dohlman et al., Ann. Rev. Biochem., ( 1991 ) 60:b53-88. When STRs are compared, a distinct spatial pattern of homology is discernible. The transmembrane domains are often the most similar, whereas the N- and C-terminal regions, and the cytoplasmic loop connecting transmembrane segments V
and VI are more divergent.
The functional significance of different STR regions has been studied by introducing point mutations (both substitutions and deletions) and by constructing chimeras of different but related STRs. Synthetic peptides corresponding to individual segments have also been tested for activity. Affinity labeling has been used to identify ligand binding sites.
In certain embodiments, if the wild-type exogenous G protein-coupled receptor cannot be made functional in yeast, it may be mutated for this purpose. A
comparison would be made of the amino acid sequences of the exogenous receptor and of the yeast receptors, and regions of high and low homology identified. Trial mutations would then be made to distinguish regions involved in ligand or G protein binding, from those necessary for functional integration in the membrane. The exogenous receptor would then be mutated in the latter region to more closely resemble the yeast receptor, until functional integration was achieved. If this were insufficient to achieve functionality, mutations would next be made in the regions involved in G protein binding.
Mutations would be made in regions involved in ligand binding only as a last resort, and then an effort would be made to preserve ligand binding by making conservative substitutions whenever possible. For example, the V-VI loop of a heterologous G protein coupled receptor could be replaced with that of the yeast STE2 or STE3 receptor),.
In yet another embodiment, a compatible G protein can be provided. A
compatable G proem for use in the instant assays can include a heterologous or chimeric G protein subunit (or subunits) such as those described in the art (see e.g., PCT
PCT/US94/03143) and as discussed in more detail below.
Preferably, the yeast genome is modified so that it is unable to produce the yeast receptors which are homologous to the exogenous receptors in functional form.

A. Chemoattractant receptors An exemplary GPCR is the N-formyl peptide receptor, a classic example of a calcium mobilizing GPCR expressed by neutrophils and other phagocytic cells of the mammalian immune system (Snyderman et al. (1988) In Inflammation: Basic Principles and Clinical Correlates, pp. 309-323). N-formyl peptides of bacterial origin bind to the receptor and engage a complex activation program that results in directed cell movement, release of inflammatory granule contents, and activation of a latent NADPH oxidase which is important for the production of metabolites of molecular oxygen. This pathway initiated by receptor-ligand interaction is critical in host protection from pyogenic infections. Similar signal transduction occurs in response to the inflammatory peptides CSa and IL-8.
Two other formyl peptide receptor like (FPRL) genes have been cloned based on their ability to hybridize to a fragment of the NFPR cDNA coding sequence.
These have been named FPRL 1 (Murphy et al. ( 1992) .I. Biol Chem. 267:7637-7643) and FPRL2 (Ye et al. ( 1992) Biochem Biophys Res. Comm. I 84:582-589). FPRL2 was found to mediate calcium mobilization in mouse fibroblasts transfected with the gene and exposed to formyl peptide. In contrast, although FPRLI was found to be 69%
identical in amino acid sequence to NFPR, it did not bind prototype N-formyl peptides ligands when expressed in heterologous cell types. This lead to the hypothesis of the existence of an as yet unidentified ligand for the FPRL 1 orphan receptor (Murphy et al.
supra).
B. G proteins In the case of an exogenous G-protein coupled receptor, the yeast cell must be able to produce a G protein which is activated by the exogenous receptor, and which can in turn activate the yeast effector(s). The art suggests that the endogenous yeast Ga subunit (e.g., GPA) will be often be sufficiently homologous to the "cognate"
Ga subunit which is natively associated with the exogenous receptor for coupling to occur.
More likely, it will be necessary to genetically engineer the yeast cell to produce a foreign Ga subunit which can properly interact with the exogenous receptor.
For example, the Ga subunit of the yeast G protein may be replaced by the Ga subunit natively associated with the exogenous receptor.
Dietzel and Kurjan, ( I 987) Cell, 50:1001 ) demonstrated that rat Gas functionally coupled to the yeast G(3y complex. However, rat Gai2 complemented only when substantially overexpressed, while Ga0 did not complement at all. Kang, et al., Mol. Cell. Biol., (1990)10:2582). Consequently, with some foreign Ga subunits, it is WO 98/13513 PCT/US97t17159 not feasible to simply replace the yeast Ga.
If the exogenous G protein coupled receptor is not adequately coupled to yeast G[3y by the Ga subunit natively associated with the receptor, the Ga subunit may be modified to improve coupling. These modifications often will take the form of mutations which increase the resemblance of the Ga subunit to the yeast Ga while decreasing its resemblance to the receptor-associated Ga. For example, a residue may be changed so as to become identical to the corresponding yeast Ga residue, or to at least belong to the same exchange group of that residue. After modification, the modified Ga subunit might or might not be "substantially homologous" to the foreign and/or the yeast Ga subunit.
The modifications are preferably concentrated in regions of the Ga which are likely to be involved in G~3y binding. In some embodiments, the modifications will take the form of replacing one or more segments of the receptor-associated Ga with the corresponding yeast Ga segment(s), thereby forming a chimeric Ga subunit. In other embodiments, point mutations may be sufficient.
This chimeric Ga subunit will interact with the exogenous receptor and the yeast G(3y complex, thereby permitting signal transduction. While use of the endogenous yeast G(3y is preferred, if a foreign or chimeric G~iy is capable of transducing the signal to the yeast effector, it may be used instead.
C. Ga Structure Some aspects of Ga structure are relevant to the design of modified Ga subunits. The amino terminal 66 residues of GPA1 are aligned with the cognate domains of human Gas, Gai2, Gai3, Gal6 and transducin. In the GPA4IGa hybrids, the amino terminal 41 residues (derived from GPA 1 ) are identical, end with the sequence-LEKQRDKNE- and are underlined for emphasis. All residues following the glutamate (E) residue at position 41 are contributed by the human Ga subunits, including the consensus nucleotide binding motif -GxGxxG-. Periods in the sequences indicate gaps that have been introduced to maximize alignments in this region.
Codon bias is mammalian. For alignments of the entire coding regions of GPA1 with Gas, Gai, and GaO, Gaq and Gaz, see Dietzel and Kurjan (1987, Cell 50:573) and Lambright, et al. (1994, Nature 369:621-628). Additional sequence information is provided by Mattera, et al. ( 1986, FEBS Lett 206:36-41 ), Bray, et al. ( 1986, Proc.
Natl. Acad Sci USA 83:8893-8897) and Bray, et al. (1987, Proc Natl. Acad Sci USA 84:5115-5119).
The gene encoding a G protein homolog of S. cerevisiae was cloned independently by Dietzel and Kurjan (supra) (SCGI) and by Nakafuku, et al.
(1987 Proc Natl Acad Sci 84:2140-2144) (GPA 1 ). Sequence analysis revealed a high degree of homology between the protein encoded by this gene and mammalian Ga. GPA1 encodes a protein of 472 amino acids, as compared with approximately 340-350 a.a. for most mammalian Ga subunits in four described families, Gas, Gai, Gaq and Gal2/13.
Nevertheless, GPA 1 shares overall sequence and structural homology with all Ga proteins identified to date. The highest overall homology in GPAI is to the Gai family {48% identity, or 65% with conservative substitutions) and the lowest is to GQS (33%
identity, or 5 I % with conservative substitutions) (Nakafuku, et al., supra).
The regions of high sequence homology among Ga subunits are dispersed throughout their primary sequences, with the regions sharing the highest degree of homology mapping to sequence that comprises the guanine nucleotide binding/GTPase domain. This domain is structurally similar to the a(3 fold of ras proteins and the protein synthesis elongation factor EF-Tu. This highly conserved guanine nucleotide-binding domain consists of a six-stranded (3 sheet surrounded by a set of five a-helices. It is within these (3 sheets and a helices that the highest degree of conservation is observed among all Ga proteins, including GPAI. The least sequence and structural homology is found in the intervening loops between the (3 sheets and a helices that define the core GTPase domain. There are a total of four "intervening loops" or "inserts"
present in all Ga subunits. In the crystal structures reported to date for the GDP- and GTPyS-liganded forms of bovine rod transducin (Noel, et al. (1993) Nature 366:654-663);
(Lambright, et al. (1994) Nature 369:621-628), the loop residues are found to be outside the core GTPase structure. Functional roles for these loop structures have been established in only a few instances. A direct role in coupling to phosphodiesterase-y has been demonstrated for residues within inserts 3 and 4 of Gat (Rarick, et al. (1992) Science 256:1031-1033); (Artemyev, et al. (1992) J. Biol. Chem. 267:25067-25072), while a "GAP-like" activity has been ascribed to the largely a-helical insert 1 domain of GaS
(Markby, et al. ( I 993) Science 262:1805-1901 ).
While the amino- and carboxy-termini of Ga subunits do not share striking homology either at the primary, secondary, or tertiary levels, there are several generalizations that can be made about them. First, the amino termini of Ga subunits have been implicated in the association of Ga with G(3y complexes and in membrane association via N-terminal myristoylation. In addition, the carboxy-termini have been implicated in the association of Ga(3y heterotrimeric complexes with G protein-coupled receptors (Sullivan, et al. (1987) Nature 330:758-760); West, et al. (1985) J.
Biol. Chem.
260:14428-14430); (Conklin, et al. (1993)Nature 363:274-276); (Kallal and Kurjan.
1997. Mol. Cell. Biol. 17:2897). Data in support of these generalizations about the function of the N-terminus derive from several sources, including both biochemical and genetic studies.
Figure 1 shows the amino terminal 66 residues of GPA 1 aligned with the cognate domains of human Gas, Gai2, Gai3, Ga 16 and transducin. In the GPA4IGa hybrids, the amino terminal 41 residues (derived from GPA1) are identical, end with the sequence-LEKQRDKNE- (SEQ ID NO: 47). All residues following the glutamate (E) residue at position 41 are contributed by the human Ga subunits, including the consensus nucleotide binding motif shown in the amino acid sequence -GxGxxG-.
Periods in the sequences indicate gaps that have been introduced to maximize alignments in this region. Codon bias is mammalian. For alignments of the entire coding regions of GPA I with Gas, Gai, and GaO, Gaq and Gaz, see Dietzel and Kurjan ( 1987, Cell 50:573) and Lambright, et al. ( 1994, Nature 369:621-628).
Additional sequence information is provided by Mattera, et al. ( 1986, FEBS Lett 206:36-41 ), Bray, et al. (1986, Proc. Natl. Acad. Sci USA 83:8893-8897) and Bray, et al. (1987, Proc Natl.
Acad Sci USA 84:5115-5119).
In other biochemical studies aimed at examining the role of the amino-terminus of Ga in driving the association between Ga and G(3y subunits, proteolytically or genetically truncated versions of Ga subunits were assayed for their ability to associate with Gay complexes, bind guanine nucleotides and/or to activate effector molecules. In all cases, Ga subunits with truncated amino termini were deficient in all three functions (Graf, et al. ( 1992) J. Biol. Chem. 267:24307-24314); (Journot, et al. ( 1990) J. Biol.
Chem. 265:9009-9015); and (Veer, et al. (1988) J. Biol. Chem 263:8996-9000).
Slepak, et al. (1993, J. Biol. Chem. 268:1414-1423) reported a mutational analysis of the N-terminal 56 a.a. of mammalian Gao expressed in Escherichia colt. Molecules with an apparent reduced ability to interact with exogenously added mammalian G(3y were identified in the mutant library. As the authors pointed out, however, the assay used to screen the mutants the extent of ADP-ribosylation of the mutant Ga by pertussis toxin was not a completely satisfactory probe of interactions between Ga and G(3y.
Mutations identified as inhibiting the interaction of the subunits, using this assay, may still permit the complexing of Ga and G~3y while sterically hindering the ribosylation of Ga by toxin. Genetic studies examined the role of amino-terminal determinants of Ga in heterotrimer subunit association have been carried out in both yeast systems using GPAI-mammalian Ga hybrids (Kang, et al. {1990) Mol. Cell. Biol. 10:2582-2590) and in mammalian systems using Gai/Gas hybrids (Russell and Johnson (1993) Mol.
Pharmacol. 44:255-263). In the former studies, gene fusions, composed of yeast GPAI
and mammalian Ga sequences were constructed by Kang, et al. (supra) and assayed for their ability to complement a gpal null phenotype (i.e., constitutive activation of the pheromone response pathway) in S. cerevisiae. Kang, et al. demonstrated that wild type mammalian Gas, Gai but not Gao proteins are competent to associate with yeast Ga and suppress the gpal null phenotype, but only when overexpressed. Fusion proteins containing the amino-terminal 330 residues of GPAI sequence linked to 160, 143, or 142 residues of the mammalian Gas, Gai and Gao carboxyl-terminal regions, respectively, also coupled to the yeast mating response pathway when overexpressed on high copy plasmids with strong inducible (CUP) or constitutive (PGK) promoters. All three of these hybrid molecules were able to complement the gpal null mutation in a growth arrest assay, and were additionally able to inhibit afactor responsiveness and mating in tester strains. These last two observations argue that hybrid yeast-mammalian Ga subunits are capable of interacting directly with, yeast G~iy, thereby disrupting the normal function of the yeast heterotrimer. Fusions containing the amino terminal domain of Gas, Gai or Gao, however, did not complement the gpal null phenotype, indicating a requirement for determinants in the amino terminal 330 amino acid residues of GPAI for association and sequestration of yeast G(3y complexes. Taken together, these data suggest that determinants in the amino terminal region of Ga subunits determine not only the ability to associate with G(3y subunits in general, but also with specific G(3~y subunits in a species-restricted manner.
Hybrid Gai/Gas subunits have been assayed in mammalian expression systems (Russell and Johnson (supra). In these studies, a large number of chimeric Ga subunits were assayed for an ability to activate adenylyl cyclase, and therefore, indirectly, for an ability to interact with G(3y(i.e., coupling of Ga to G~3y= inactive cyclase;
uncoupling of Ga from G(3y = active cyclase). From these studies a complex picture emerged in which determinants in the region between residues 25 and 96 of the hybrids were found to determine the state of activation of these alleles as reflected in their rates of guanine nucleotide exchange and GTP hydrolysis and the extent to which they activated adenylyl cyclase in vivo. These data could be interpreted to support the hypothesis that structural elements in the region between the amino terminal methionine and the ~I sheet identif ed in the crystal structure of Gat (see Noel, et al. supra and Lambright, et al.
supra) are involved in determining the state of activity of the heterotrimer by (1) driving association/dissociation between Ga and G(3y subunits; (2) driving GDP/GTP
exchange.
While there is no direct evidence provided by these studies to support the idea that residues in this region of Ga and residues in G(3~y subunits contact one another, the data nonetheless provide a positive indication for the construction of hybrid Ga subunits that retain function. There is, however, a negative indicator that derives from this work in that some hybrid constructs resulted in constitutive activation of the chimeric proteins (i.e., a loss of receptor-dependent stimulation of G~3y dissociation and effector activation).
D. Construction of chimeric Ga subunits.
In designing Ga subunits capable of transmitting, in yeast, signals originating at mammalian G protein-coupled receptors, two general desiderata were recognized.
First, the subunits should retain as much of the sequence of the native mammalian proteins as possible. Second, the level of expression for the heterologous components should approach, as closely as possible, the level of their endogenous counterparts.
The results described by King, et al. (1990, Science 250:121-123) for expression of the human ~32-adrenergic receptor and Gas in yeast, taken together with negative results obtained by Kang, et al. (supra) with full-length mammalian Ga subunits other than Gas, led us to the following preferences for the development of yeast strains in which mammalian G
protein-coupled receptors could be linked to the pheromone response pathway.
1. Mammalian Ga subunits will be expressed using the native sequence of each subunit or, alternatively, as minimal gene fusions with sequences from the amino-terminus of GPA1 replacing the homologous residues from the mammalian Ga subunits.
2. Mammalian Ga subunits will be expressed from the GPA1 promoter either on low copy plasmids or after integration into the yeast genome as a single copy gene.
3. Endogenous G~3y subunits will be provided by the yeast STE4 and STE 18 loci.
E Site-Directed Mutagenesis versus Random Mutagenesis There are two general approaches to solving structure-function problems of the sort presented by attempts to define the determinants involved in mediating the association of the subunits that comprise the G protein heterotrimer. The first approach, discussed above with respect to hybrid constructs, is a rational one in which specific mutations or alterations are introduced into a molecule based upon the available experimental evidence. In a second approach, random mutagenesis techniques, coupled with selection or screening systems, are used to introduce large numbers of mutations into a molecule, and that collection of randomly mutated molecules is then subjected to a selection for the desired phenotype or a screen in which the desired phenotype can be observed against a background of undesirable phenotypes. With random mutagenesis one can mutagenize an entire molecule or one can proceed by cassette mutagenesis. In the former instance, the entire coding region of a molecule is mutagenized by one of several methods (chemical, PCR, doped oligonucleotide synthesis) and that collection of randomly mutated molecules is subjected to selection or screening procedures.
Random mutagenesis can be applied in this way in cases where the molecule being studied is relatively small and there are powerful and stringent selections or screens available to discriminate between the different classes of mutant phenotypes that will inevitably arise. In the second approach, discrete regions of a protein, corresponding either to defined structural (i.e. a-helices, /3 -sheets, turns, surface loops) or functional determinants (e.g., catalytic clefts, binding determinants, transmembrane segments) are subjected to saturating or semi-random mutagenesis and these mutagenized cassettes are re-introduced into the context of the otherwise wild type allele. Cassette mutagenesis is most useful when there is experimental evidence available to suggest a particular function for a region of a molecule and there is a powerful selection and/or screening approach available to discriminate between interesting and uninteresting mutants.
Cassette mutagenesis is also useful when the parent molecule is comparatively large and the desire is to map the functional domains of a molecule by mutagenizing the molecule in a step-wise fashion, i.e. mutating one linear cassette of residues at a time and then assaying for function.
The present invention contemplates applying random mutagenesis in order to further delineate the determinants involved in Ga-G(3y association. Random mutagenesis may be accomplished by many means, including:
1. PCR mutagenesis, in which the error prone Taq polymerase is exploited to generate mutant alleles of Ga subunits, which are assayed directly in yeast for an ability to couple to yeast G~3y.
2. Chemical mutagenesis, in which expression cassettes encoding Ga subunits are exposed to mutagens and the protein products of the mutant sequences are assayed directly in yeast for an ability to couple to yeast G ~3y.
3. Doped synthesis of oligonucleotides encoding portions of the Ga gene.
4. In vivo mutagenesis, in which random mutations are introduced into the coding region of Ga subunits by passage through a mutator strain of E coli, XLl-Red (mutDS mutS mutT) (Stratagene, Menasa, WI).
The random mutagenesis may be focused on regions suspected to be involved in Ga-G(3y association as discussed in the next section. Random mutagenesis approaches are feasible for two reasons. First, in yeast one has the ability to construct stringent screens and facile selections (growth vs. death, transcription vs. lack of transcription) that are not readily available in mammalian systems. Second, when using yeast it is possible to screen efficiently through thousands of transformants rapidly.
Cassette mutagenesis is immediately suggested by the observation (see infra) that the hybrids couple to the pheromone response pathway. This relatively small region of Ga subunits represents a reasonable target for this type of mutagenesis. Another region that may be amenable to cassette mutagenesis is that defining the surface of the switch region of Ga subunits that is solvent-exposed in the crystal structures of Gai and transducin. From the data described below, this surface may contain residues that are in direct contact with yeast Gj3y subunits, and may therefore be a reasonable target for mutagenesis.
F. Rational Design of Chimeric Ga Subunits Several classes of rationally designed GPAI-mammalian Ga hybrid subunits have been tested for the ability to couple to yeast ~y. The first, and largest, class of hybrids are those that encode different lengths of the GPAI amino terminal domain in place of the homologous regions of the mammalian Ga subunits. This class of hybrid molecules includes GPAgAMHI ~ GPA41, GPAID, and GPALW hybrids, described below. The rationale for constructing these hybrid Ga proteins is based on results, described above, that bear on the importance of the amino terminal residues of Ga in mediating interaction with G~3y.
Preferably, the yeast Ga subunit is replaced by a chimeric Ga subunit in which a portion, e.g., at least about 20, more preferably at least about 40, amino acids, which is substantially homologous with the corresponding residues of the amino terminus of the yeast Ga, is fused to a sequence substantially homologous with the main body of a mammalian (or other exogenous) Ga. While 40 amino acids is the suggested starting point, shorter or longer portions may be tested to determine the minimum length required for coupling to yeast G(3y and the maximum length compatible with retention of coupling to the exogenous receptor. It is presently believed that only the final 10 or 20 amino acids at the carboxy terminus of the Ga subunit are required for interaction with the receptor.
GPABAMH 1 h-- b~~ Kang et al. supra. described hybrid G a subunits encoding the amino terminal 310 residues of GPAI fused to the carboxyl terminal 160, 143 and 142 residues, respectively, of GaS, Gai2, and Gao. In all cases examined by Kang et al., the hybrid proteins were able to complement the growth arrest phenotype of gpal strains. These findings have been confirmedand, in addition, have constructed and tested hybrids between GPAI and Gai3, Gaq and Gal6. All hybrids of this type that have been tested functionally complement the growth arrest phenotype of gpal strains.

GPA41 h~rbrids. The rationale for constructing a minimal hybrid encoding only 41 amino acids of GPAI relies upon the biochemical evidence for the role of the amino-terminus of Ga subunits discussed above, together with the following observation. G (3 and Gy subunits are known to interact via a- helical domains at their respective amino-termini (Pronin, et al. ( 1992) Proc. Natl. Acad. Sci. USA
89:6220-6224); Garritsen, et a1.1993). The suggestion that the amino termini of Ga subunits may form an helical coil and that this helical coil may be involved in association of Ga with G~3y (Masters et al (1986) Protein Engineering 1:47-54); Lupas et a1.(1992) FEBS Lett.
314:105-108) leads to the hypothesis that the three subunits of the G-protein heterotrimer interact with one another reversibly through the winding and unwinding of their amino-terminal helical regions. A mechanism of this type has been suggested, as well, from an analysis of leucine zipper mutants of the GCN4 transcription factor (Harbury, et al. (1993) Science 262:1401-1407). The rationale for constructing hybrids like those described by Kang, et al. supra., that contain a majority of yeast sequence and only minimal mammalian sequence, derives from their ability to function in assays of coupling between Ga and G(3y subunits. However, these chimeras had never been assayed for an ability to couple to both mammalian G protein-coupled receptors and yeast G(3y subunits, and hence to reconstitute a hybrid signaling pathway in yeast.
GPA41 hybrids that have been constructed and tested include Gas, Gai2, Gai3, Gaq, Gaoa, Gaob and Ga 16. Hybrids of Gas, Gai2, Gai3, and Ga 16 functionally complement the growth arrest phenotype of gpal strains, while GPA41 hybrids of Gaoa and Gaob do not. In addition to being tested in a growth arrest assay, these constructs have been assayed in the more sensitive transcriptional assay for activation of a fuslp-HIS3 gene. In both of these assays, the GPA41-Gas hybrid couples less well than the GPa41-i2, -i3, and -16 hybrids, while the GPa41 -oa, and -ob hyrids do not function in either assay.
Several predictive algorithms indicate that the amino terminal domain up to the highly conserved sequence motif LLLLGAGESG- (SEQ ID N0:46) (the first L in this motif is residue 43 in GPAl) forms a helical structure with amphipathic character.
Assuming that a heptahelical repeat unit, the following hybrids between GPA1 and GaS
can be used to define the number of helical repeats in this motif necessary for hybrid function:
GPAI-7/GasB-394 GPA 1-14/Gas 15-394 GPAI-21 /Gas22-3 94 GPAI-28/Gas29-394 GPA 1-35/Gas36-394 GPAI-42/Gas43-394 In these hybrids, the prediction is that the structural repeat unit in the amino terminal domain up to the tetra-leucine motif is 7, and that swapping sequences in units of 7 will in effect amount to a swap of unit turns of turns of the helical structure that comprises this domain.
A second group of "double crossover"' hybrids of this class are those that are aligned on the first putative heptad repeat beginning with residue G I 1 in GPA 1. In these hybrids, helical repeats are swapped from GPA 1 into a GaS backbone one heptad repeat unit at a time.
GaS I -10/GPA 11- I 7/Gas 18-3 94 Ga S 1- I 7/GPA I 8-24/GaS25-394 GaS I -17/GPA25-31 /GaS32-394 GaS?-17/GPA32-38/GaS39-394 The gap that is introduced between residues 9 and 10 in the GaS sequence is to preserve the alignment of the -LLLLGAGE- (amino acids 1-8 of SEQ ID NO: 46) sequence motif. This class of hybrids can be complemented by cassette mutagenesis of each heptad repeat followed by screening of these collections of "heptad"
libraries in standard coupling assays.
A third class of hybrids based on the prediction that the amino terminus forms a helical domain with a heptahelical repeat unit are those that effect the overall hydrophobic or hydrophilic character of the opposing sides of the predicted helical structure (See Lupas et al. supra). In this model, the a and d positions of the heptad repeat abcdefg are found to be conserved hydrophobic residues that define one face of the helix, while the a and g positions define the charged face of the helix.
In this class of hybrids, the sequence of the GaS parent is maintained except for specific substitutions at one or more of the following critical residues to render the different helical faces of GaS
more "GPA I -like"

+I-10 EIOG

EISP

This collection of single mutations could be screened for coupling efficiency to yeast G(3y and then constructed in combinations (double and greater if necessary).
A fourth class of hybrid molecules that span this region of GPA1-Ga hybrids are those that have junctions between GPAI and Ga subunits introduced by three primer PCR. In this approach, the two outside primers are encoded by sequences at the initiator methionine of GPA 1 on the 5' side and at the tetraleucine motif of GaS (for example) on the 3' side. A series of functional primers spanning different functional points can be mixed with the outside primers to make a series of molecules each with different amounts of GPA 1 and GaS sequences, respectively.
GPAID and GPALW h brids. The regions of high homology among G(3y subunits that have been identified by sequence alignment are interspersed throughout the molecule. The G 1 region containing the highly conserved -GSGESGDST- motif is followed immediately by a region of very low sequence consevation, the "i1" or insert I
region. Both sequence and length vary considerably among the i1 regions of the Ga subunits. By aligning the sequences of Ga subunits, the conserved regions bounding the i1 region were identified and two additional classes of GPAI-Ga hybrids were constructed. The GPAID hybrids encode the amino terminal 102 residues of GPA1 (up to the sequence -QARKLGIQ-) fused in frame to mammalian Ga subunits, while the GPALW hybrids encode the amino terminal 244 residues of GPAI (up to the sequence -LIHEDIAKA- in GPA 1 ). The reason for constructing the GPAID and GPALW hybrids was to test the hypothesis that the i1 region of GPAI is required for mediating the interaction of GPAI with yeast G(3y subunits, for the stable expression of the hybrid molecules, or for function of the hybrid molecules. The GPAID hybrids contain the amino terminal domain of GPAI fused to the i1 domain of mammalian subunits, and therefore do not contain the GPA1 i1 region, while the GPALW hybrids contain the amino terminal 244 residues of GPA 1 including the entire i1 region (as defined by sequence alignments). Hybrids of both GPAID and GPALW classes were constructed for GaS, C-ai2, Gai3, Gaoa, and Ga 16; none of these hybrids complemented the gpal growth arrest phenotype.
Subsequent to the construction and testing of the GPAID and GPALW classes of hybrids, the crystal structures of Gtransducin in both the GDP and GTPyS-liganded form, and the crystal structure of several Gail variants in the GTP~yS-liganded and GDP-A1F4 forms were reported (Noel et al. supra; Lambright et al. supra; and Coleman et a1.(1994) Science 265:1405-1412). The crystal structures reveal that the ilregion defined by sequence alignment has a conserved structure that is comprised of six alpha helices in a rigid array, and that the junctions chosen for the construction of the GPAID
and GPALw hybrids were not compatible with conservation of the structural features of the i1 region observed in the crystals. The junction chosen for the GPAID
hybrids falls in the center of the long aA helix; chimerization of this helix in all likelihood destabilizes it and the protein structure in general. The same is true of the junction chosen for the GPALW hybrids in which the crossover point between GPA1 and the mammalian Ga subunit falls at the end of the short aC helix and therefore may distort it and destabilize the protein.
The failure of the GPAID and GPALw hybrids is predicted to be due to disruption of critical structural elements in the i1 region as discussed above. Based upon new alignments and the data presented in Noel et al (supra), Lambright et al (supra), and Coleman et al (supra), this problem can be averted with the ras-like core domain and the i1 helical domain are introduced outside of known structural elements like alpha-helices.
Hybrid A GaSI-67/GPA66-299/GaS203-394 This hybrid contains the entire i1 insert of GPAI interposed into the GaS sequence.
Hybrid B GPAI-41/GaS4443-67/GPA66-299/GaS203-394 This hybrid contains the amino terminal 41 residues of GPA1 in place of the 42 amino terminal residues of GaS found in Hybrid A.
Gas Hybrids. There is evidence that the "switch region" encoded by residues 171-237 of Ga transducin (using the numbering of (Noel et al (supra) also plays a role in G(3y coupling. First, the G226A mutation in GaS prevents the GTP-induced conformational change that occurs with exchange of GDP for GTP upon receptor activation by ligand. This residue maps to the highly conserved sequence -DVGGQ-, present in all Ga subunits and is involved in GTP hydrolysis. In both the Gat and Ga i1 crystal structures, this sequence motif resides in the loop that connects the ~3 sheet and the a2 helix in the guanine nucleotide binding core. In addition to blocking the conformational change that occurs upon GTP binding, this mutation also prevents dissociation of GTP-liganded Gas from G(3y. Second, crosslinking data reveals that a highly conserved cysteine residue in the a2 helix (C215 in Gao, C210 in Gat) can be crosslinked to the carboxy terminal region of G(3 subunits. Finally, genetic evidence (Whiteway et al. (1993) Mol Cell Biol. 14:3233-3239) identifies an important single residue in GPA1 (E307) in the j32 sheet of the core structure that may be in direct contact with ~iy. A mutation in the GPA 1 protein at this position suppresses the constitutive signalling phenotype of a variety of STE4 (G(3) dominant negative mutations that are also known to be defective in Ga-G[3y association (as assessed in two-hybrid assay in yeast as well as by more conventional genetic tests).
The hypothesis that there are switch region determinants involved in the association of Ga with G(3y has been tested by constructing a series of hybrid Ga proteins encoding portions of GPAI and GaS in different combinations.
Two conclusions may be drawn. First, in the context of the amino terminus of GaS, the GPAI switch region suppresses coupling to yeast G(3y (SGS), while in the context of the GPA 1 amino terminus the GPA1 switch region stabilizes coupling with G(3y (GP~3y-SGS). This suggests that these two regions of GPA1 collaborate to allow interactions between Ga subunits and G(3y subunits. This conclusion is somewhat mitigated by the observation that the GPA41-Gas hybrid that does not contain the GPAI
switch region is able to complement the growth arrest phenotype of gpal strains. A
quantitative difference between the behavior of the GPA41-Gas allele and the GPA~I-SGS allele has not been noted, but if this interaction is somewhat degenerate, then it may be difficult to quantitate this accurately. The second conclusion that can be drawn from these results is that there are other determinants involved in stabilizing the interaction of Ga with G~3y beyond these two regions as none of the GPAI/Gas hybrid proteins couple as efficiently to yeast G/3y as does native GPA1.
The role of the surface-exposed residues of this region may be crucial for effective coupling to yeast G(3y, and can be incorporated into hybrid molecules as follows below.
GaS-GPA-Switch GaS 1-202/GPA298-350/GaS 253-394 This hybrid encodes the entire switch region of GPA 1 in the context of GaS.
GaS-GPA-a2 GQS 1-226/GPA322-332/GQS 238-394 This hybrid encodes the a2 helix of GPAI in the context of GaS.

GPA41-GaS-GPA-a2GPAl-41/GQS43-226/GPA322-332/GQS238-394 This hybrid encodes the 41 residue amino terminal domain of GPAI and the a2 helix of GPA1 in the context of GaS.
Finally, the last class of hybrids that will be discussed here are those that alter the surface exposed residues of the X32 and J33 sheets of aS so that they resemble those of the GPA1 QS helix. These altered a2 helical domains have the following structure.
(The positions of the altered residues correspond to GaS.) These single mutations can be engineered into a GaS backbone singly and in pairwise combinations. In addition, they can be introduced in the context of both the full length GaS and the GPA41-GaS hybrid described previously. All are predicted to improve the coupling of Ga subunits to yeast G(3y subunits by virtue of improved electrostatic and hydrophobic contacts between this region and the regions of G~3 defined by Whiteway and coworkers (Whiteway et al (supra) that define sites) that interact with GPA 1 ).
In summary, the identification of hybrid Ga subunits that couple to the yeast pheromone pathway has led to the following general observations. First, all GPAgAMH 1 hybrids associate with yeast G(3y, therefore at a minimum these hybrids contain the determinants in GPA 1 necessary for coupling to the pheromone response pathway. Second, the amino terminal 41 residues of GPA 1 contain sufficient determinants to facilitate coupling of Ga hybrids to yeast G(3y in some, but not all, instances, and that some Ga subunits contain regions outside of the first 41 residues that are sufficiently similar to those in GPA 1 to facilitate interaction with GPA
1 even in the absence of the amino terminal 41 residues of GPA 1. Third, there are other determinants in the first 310 residues of GPAI that are involved in coupling Ga subunits to yeast G(3y subunits.
The various classes of hybrids noted above are not mutually exclusive. For example, a GPAl containing GPA1-41 could also feature the L203K mutation.
While, for the sake of simplicity, hybrids of yeast GPA1 and a mammalian Gas have been described, it will be appreciated that hybrids may be made of other yeast Ga subunits and/or other mammalian Ga subunits, notably mammalian Gai subunits.

Moreover, while the described hybrids are constructed from two parental proteins, hybrids of three or more parental proteins are also possible.
As shown in the Examples, chimeric Ga subunits have been especially useful in coupling receptors to Gai species.
G. Expression of Ga Kang et al. supra reported that several classes of native mammalian G~
subunits were able to interact functionally with yeast a subunits when expression of Ga was driven from a constitutively active, strong promoter (PGK) or from a strong inducible promoter (CUP). These authors reported that rat GaS, Gai2 or Gao expressed at high level coupled to yeast (3y. High level expression of mammalian Ga (i.e.
non-stoichiometric with respect to yeast (3y) is not desirable for uses like those described in this application. Reconstruction of G protein- coupled receptor signal transduction in yeast requires the signalling component of the heterotrimeric complex (G(3y) to be present stoichiometrically with Ga subunits. An excess of Ga subunits (as was required for coupling of mammalian Gait and Gao to yeast G(3y in Kang et al.) would dampen the signal in systems where G(3y subunits transduce the signal. An excess of Ga subunits raises the background level of signaling in the system to unacceptably high levels. Preferably, levels of Ga and G/3y subunits are balanced. For example, heterologous Ga subunits may be expressed from a low copy (CEN ARS) vector containing the endogenous yeast GPAI promoter and the GPA1 3' untranslated region.
The minimum criterion, applied to a heterologous Ga subunit with respect to its ability to couple functionally to the yeast pheromone pathway, is that it complement a gpal genotype when expressed from the GPAI promoter on low copy plasmids or from an integrated, single copy gene. In the work described in this application, all heterologous Ga subunits have been assayed in two biological systems. In the first assay heterologous Ga subunits are tested for an ability to functionally complement the growth arrest phenotype of gpal strains. In the second assay the transcription of a fusl-HISS reporter gene is used to measure the extent to which the pheromone response pathway is activated, and hence the extent to which the heterologous Ga subunit sequesters the endogenous yeast G(3y complex. Mammalian Gas, Gait, Gai3, Gaq, Ga 11, Ga 16, Gaoa, Gaob, and Gaz from rat, murine or human origins were expressed from a low copy, CEN ARS vector containing the GPAI promoter. Functional complementation of gpal strains was not observed in either assay system with any of these full-length Ga constructs with the exception of rat and human GaS.

H. Chimeric Yeast (3y subunits An alternative to the modification of a mammalian Ga subunit for improved signal transduction is the modification of the pertinent sites in the yeast G~
or Gy subunits. The principles discussed already with respect to Ga subunits apply, mutatis mutandis, to yeast G(3 or Gy.
For example, in certain embodiments the yeast Ste4p G(3subunit can be targetedwith cassette mutagenesis. Specifically, the region of Ste4p that encodes several of the dominant negative, signaling-defective mutations would be an excellent target for cassette mutagenesis when looking for coupling of yeast G(3y to specific mammalian Ga subunits.
V. Test Compounds Exogenously added compounds A recent trend in medicinal chemistry includes the production of mixtures of compounds, referred to as libraries. While the use of libraries of peptides is well established in the art, new techniques have been developed which have allowed the production of mixtures of other compounds, such as benzodiazepines (Bunin et al. 1992.
J. Am. Chem. Soc. 114:10987; DeWitt et al. 1993. Proc. Natl. Acad. Sci. USA
90:6909) peptoids (Zuckermann. 1994. J. Med. Chem. 37:2678) oligocarbamates (Cho et al.
1993. Science. 261:1303), and hydantoins (DeWitt et al. supra). Rebek et al.
have described an approach for the synthesis of molecular libraries of small organic molecules with a diversity of 104-105 (Carell et al. 1994. Angew. Chem. Int.
Ed. Engl.
33:2059; Carell et al. Angew. Chem. Int. Ed. Engl. 1994. 33:2061 ).
The compounds of the present invention can be obtained using any of the numerous approaches in combinatorial library methods known in the art, including:
biological libraries; spatially addressable parallel solid phase or solution phase libraries, synthetic library methods requiring deconvolution, the 'one-bead one-compound' library method, and synthetic library methods using affinity chromatography selection.
The biological library approach is limited to peptide libraries, while the other four approaches are applicable to peptide, non-peptide oligomer or small molecule libraries of compounds (Lam, K.S. Anticancer Drug Des. 1997. 12:145).
In one embodiment, the test compound is a peptide or peptidomimetic. In another, preferred embodiment, the compounds are small, organic non-peptidic compounds.
Other exemplary methods for the synthesis of molecular libraries can be found in -sz-the art, for exartiple in: Erb et al. 1994. Proc. Nail. Acad. Sci. USA
91:114??, HorwCll et al. 1996 Immunopharmacology 33:68; and in Gallop et al. 1994. J. Med. Chem.
37;1233. In addition, libraries such as chose described in the commonly owned U-S. Patent 6,037,340 can be used to provide compounds for testing in the present invention.
Libraries of compounds may be presznted in solution (e.g., Houghten (199?) Biorech~riques 13:412-421 ), or on beads (irarrl ( 199I ) Narure 354.82-84), chips (Fodor (I993~ Naeure 364:55$-s56), bacteria (Ladner USP 5,223,409), spores (Ladner USP
'409), plasmids (Cull et al. (1992) Proc Narl Acad Sci USA 89:1865-~ 869) or on phage (SCOTT and Smith (I99p) Science 249:388-390); (Devlin (I99b~Science 249:404-406);
(Cwirla et aI. (I99U) Proc. Narl. Acad Sci. 87:6378-6382); (Felici ( 1991 ) J
Mol_ Blol.
?3?:30I-310); (Ladnersupra.).
in certain embodiments, the test compounds are exogznously added to the yeast cells expressing a recombinant receptor' and compounds that modulate signal uansduction via the receptor are selected. In other embodiments, the yeast cells express the compounds to be tested. For example, a culture of the subject yeast cells cart be further modified to collectively express a peptide library as described in more detail in PCT Publication WO 94/23025 the contents of which is expressly incorporated herein by this reference.
Other types of peptide libraries may also be expressed, see, for example, U.S.
Patents 5,370,181 and 5,292,646; and PCT publication W094/ 03502). In still another embodiment, the combinatorial polypeptides arc produced from a cANA library.
Exemplary compounds which cart be screened for activity Include, but are not limited to, peptides, nucleic acids, carbohydrates, small organic molecules, and natural product exuact libraries. In such embodiments, both compounds which agonize or antagonize the receptor- or channel-mediated signaling function can be selected and identified.
Peptide Libraries In certain embodiments, yeast cells can be engineered to product the compounds to be tested. This assay system has the advantage of increasing the effective concentration of the compound to be tested. In one embodiment, a rnzthod such as that described in WO 94/?30?5 can be utilized.
Other methods can also be used. Far example, peptide libraries are systems which simultaneously display, in a form which permits interaction with a target, a highly diverse and numerous collection of peptides. These peptides may be presented in solution (Houghten ( 1992) Biotechnigues I 3 :4 I 2-421 ), or on beads (Lam ( 1991 ) Nature 354:82-84), chips (Fodor {1993) Nature 364:555-556), bacteria (Ladner USP
5,223,409), spores (Ladner USP '409), plasmids (Cull et al. (1992) Proc Natl Acad Sci USA 89:1865-1869) or on phage (Scott and Smith (1990) Science 249:386-390);
(Devlin (1990)Science 249:404-406); (Cwirla et al. (1990) Proc. Nat). Acad. Sci.
87:6378-6382); (Felici ( I 991 ) J. Mol. Biol. 222:301-310); (Ladner supra. ). Many of these systems are limited in terms of the maximum length of the peptide or the composition of the peptide (e.g., Cys excluded). Steric factors, such as the proximity of a support, may interfere with binding. Usually, the screening is for binding in vitro to an artificially presented target, not for activation or inhibition of a cellular signal transduction pathway in a living cell. While a cell surface receptor may be used as a target, the screening will not reveal whether the binding of the peptide caused an allosteric change in the conformation of the receptor.
The Ladner et al. patent, USSN 5,096,815, describes a method of identifying novel proteins or polypeptides with a desired DNA binding activity. Semi-random ("variegated") DNA encoding a large number of different potential binding proteins is introduced, in expressible form, into suitable yeast cells. The target DNA
sequence is incorporated into a genetically engineered operon such that the binding of the protein or polypeptide will prevent expression of a gene product that is deleterious to the gene under selective conditions. Cells which survive the selective conditions are thus cells which express a protein which binds the target DNA. While it is taught that yeast cells may be used for testing, bacterial cells are preferred. The interactions between the protein and the target DNA occur only in the cell (and then only in the nucleus), not in the periplasm or cytoplasm, and the target is a nucleic acid, and not a receptor protein.
Substitution of random peptide sequences for functional domains in cellular proteins permits some determination of the specific sequence requirements for the accomplishment of function. Though the details of the recognition phenomena which operate in the localization of proteins within cells remain largely unknown, the constraints on sequence variation of mitochondria) targeting sequences and protein secretion signal sequences have been elucidated using random peptides (Lemire et al., J.
Biol. Chem.(1989) 264, 20206 and Kaiser et al. (1987) Science 235:312, respectively).
In certain embodiments of the instant invention, the compounds tested are in the form of peptides from a peptide library. The peptide library of the present invention takes the form of a cell culture, in which essentially each cell expresses one, and usually only one, peptide of the library. While the diversity of the library is maximized if each cell produces a peptide of a different sequence, it is usually prudent to construct the library so there is some redundancy. Depending on size, the combinatorial peptides of the library can be expressed as is, or can be incorporated into larger fusion proteins. The fusion protein can provide, for example, stability against degradation or denaturation, as well as a secretion signal if secreted. In an exemplary embodiment of a library for intracellular expression, e.g., for use in conjunction with intracellular target receptors, the polypeptide library is expressed as thioredoxin fusion proteins (see, for example, U.S. Patents 5,270,181 and 5,292,646; and PCT publication W094/ 02502). The combinatorial peptide can be attached one the terminus of the thioredoxin protein, or, for short peptide libraries, inserted into the so-called active loop.
In one embodiment, the peptide library is derived to express a combinatorial library of polypeptides which are not based on any known sequence, nor derived from cDNA. That is, the sequences of the library are largely random. In preferred embodiments, the combinatorial polypeptides are in the range of 3-100 amino acids in length, more preferably at least 5-50, and even more preferably at least 10, 13, 15, 20 or 25 amino acid residues in length. Preferably, the polypeptides of the library are of uniform length. It will be understood that the length of the combinatorial peptide does not reflect any extraneous sequences which may be present in order to facilitate expression, e.g., such as signal sequences or invariant portions of a fusion protein.
In another embodiment, the peptide library is derived to express a combinatorial library of polypeptides which are based at least in part on a known polypeptide sequence or a portion thereof (not a cDNA library). That is, the sequences of the library is semi-random, being derived by combinatorial mutagenesis of a known sequence. See, for example, Ladner et al. PCT publication WO 90/02909; Garrard et al., PCT
publication WO 92/09690; Marks et al. (1992) J. Biol. Chem. 267:16007-16010; Griffths et al.
(1993) EMBO J 12:725-734; Clackson et al. (1991) Nature 352:624-628; and Barbas et al. ( 1992) PNAS 89:4457-4461. Accordingly, polypeptide(s) which are known ligands for a target receptor can be mutagenized by standard techniques to derive a variegated library of polypeptide sequences which can further be screened for agonists and/or antagonists. For example, the surrogate ligand identified for FPRL-1, e.g., the Ser-Leu-Leu-Trp-Leu-Thr-Cys-Arg-Pro-Trp-Glu-Ala-Met peptide, can be mutagenized to generate a library of peptides with some relationship to the original tridecapeptide. This library can be expressed in a reagent cell of the present invention, and other receptor activators can be isolated from the library. This may permit the identification of even more potent FPRL-1 surrogate ligands.
Alternatively, the library can be expressed under conditions wherein the cells are -5 $-in contact with the original tridecapeptide, e.g., the FPRL-1 receptor is being induced by that surrogate ligand. Peptides from an expressed library can be isolated based on their ability to potentiate the induction, or to inhibit the induction, caused by the surrogate ligand. The latter of course will identify potential antagonists of chemoattractant receptors. In still other embodiments, the surrogate ligand can be used to screen exogenous compound libraries (peptide and non-peptide) which, by modulating the activity of the identified surrogate, will presumably also similarly effect the native ligand's effect on the target receptor. In such embodiments, the surrogate ligand can be applied to the cells, though is preferably produced by the reagent cell, thereby providing an autocrine cell.
In still another embodiment, the combinatorial polypeptides are produced from a cDNA library.
In a preferred embodiment of the present invention, the yeast cells collectively produce a "peptide library", preferably including at least 103 to 10~
different peptides, so that diverse peptides may be simultaneously assayed for the ability to interact with the exogenous receptor. In an especially preferred embodiment, at least some peptides of the peptide library are secreted into the periplasm, where they may interact with the "extracellular" binding sites) of an exogenous receptor. They thus mimic more closely the clinical interaction of drugs with cellular receptors. This embodiment optionally may be further improved (in assays not requiring pheromone secretion) by preventing pheromone secretion, and thereby avoiding competition between the peptide and the pheromone for signal peptidase and other components of the secretion system.
In certain embodiments of the present invention, the peptides of the library are encoded by a mixture of DNA molecules of different sequence. Each peptide-encoding DNA molecule is ligated with a vector DNA molecule and the resulting recombinant DNA molecule is introduced into a yeast cell. Since it is a matter of chance which peptide encoding DNA molecule is introduced into a particular cell, it is not predictable which peptide that cell will produce. However, based on a knowledge of the manner in which the mixture was prepared, one may make certain statistical predictions about the mixture of peptides in the peptide library.
The peptides of the library can be composed of constant and variable residues.
If the nth residue is the same for all peptides of the library, it is said to be constant. If the nth residue varies, depending on the peptide in question, the residue is a variable one.
The peptides of the library will have at least one, and usually more than one, variable residue. A variable residue may vary among any of two to all twenty of the genetically encoded amino acids; the variable residues of the peptide may vary in the same or dif ferent manner. Moreover, the frequency of occurrence of the allowed amino acids at a particular residue position may be the same or different. The peptide may also have one or more constant residues.
There are two principal ways in which to prepare the required DNA mixture. In one method, the DNAs are synthesized a base at a time. When variation is desired, at a base position dictated by the Genetic Code, a suitable mixture of nucleotides is reacted with the nascent DNA, rather than the pure nucleotide reagent of conventional polynucleotide synthesis.
The second method provides more exact control over the amino acid variation.
First, trinucleotide reagents are prepared, each trinucleotide being a codon of one (and only one) of the amino acids to be featured in the peptide library. When a particular variable residue is to be synthesized, a mixture is made of the appropriate trinucleotides and reacted with the nascent DNA. Once the necessary "degenerate" DNA is complete, it must be joined with the DNA sequences necessary to assure the expression of the peptide, as discussed in more detail below, and the complete DNA construct must be introduced into the yeast cell.
In embodiments in which the test compounds it may be desirable to express such peptides in the context of a leader sequence. Yeast cells are bounded by a lipid bilayer called the plasma membrane. Between this plasma membrane and the cell wall is the periplasmic space. Peptides secreted by yeast cells cross the plasma membrane through a variety of mechanisms and thereby enter the periplasmic space. The secreted peptides are then free to interact with other molecules that are present in the periplasm or displayed on the outer surface of the plasma membrane. The peptides then either undergo re-uptake into the cell, diffuse through the cell wall into the medium, or become degraded within the periplasmic space.
The test polypeptide library may be secreted into the periplasm by any of a number of exemplary mechanisms, depending on the nature of the expression system to which they are linked. In one embodiment, the peptide may be structurally linked to a yeast signal sequence, such as that present in the a-factor precursor, which directs secretion through the endoplasmic reticulum and Golgi apparatus. Since this is the same route that the receptor protein follows in its journey to the plasma membrane, opportunity exists in cells expressing both the receptor and the peptide library for a specific peptide to interact with the receptor during transit through the secretory pathway. This has been postulated to occur in mammalian cells exhibiting autocrine activation. Such interaction could yield activation of the response pathway during transit, which would still allow identification of those cells expressing a peptide agonist.

For situations in which peptide antagonists to externally applied receptor agonist axe sought, this system would still be effective, since both the peptide antagonist and receptor would be delivered to the outside of the cell in concert. Thus, those cells producing an antagonist would be selectable, since the peptide antagonist would be properly and timely situated to prevent the receptor from being stimulated by the externally applied agonist.
An alternative mechanism for delivering peptides to the periplasmic space is to use the ATP-dependent transporters of the STE6/MDRl class. This transport pathway and the signals that direct a protein or peptide to this pathway are not as well characterized as is the endoplasmic reticulum-based secretory pathway.
Nonetheless, these transporters apparently can efficiently export certain peptides directly across the plasma membrane, without the peptides having to transit the ER/Golgi pathway.
It is anticipated that at least a subset of peptides can be secreted through this pathway by expressing the library in context of the a-factor prosequence and terminal tetrapeptide.
The possible advantage of this system is that the receptor and peptide do not come into contact until both are delivered to the external surface of the cell. Thus, this system strictly mimics the situation of an agonist or antagonist that is normally delivered from outside the cell. Use of either of the described pathways is within the scope of the invention. The present invention does not require periplasmic secretion, or, if such secretion is provided, any particular secretion signal or transport pathway.
VI. Screening and Selection The ability of particular test compounds to modulate a signal transduction activity of the receptor of interest can be scored for by detecting up or down-regulation of a detection signal. For example, alterations in the endogenous yeast second messenger generation (e.g. GTPase activity, phospholipid hydrolysis, or protein phosphorylation patterns or enzyme activity) can be measured directly.
Alternatively, the use of an indicator gene or a heterologous reporter gene can provide a convenient readout. In any event, a change in the detection signal can be used to facilitate identification of compounds which modulate signaling via the receptor.
Second Messenger Production In certain embodiments, changes in intracellular second messenger pathways can be detected biochemically, i.e., by measuring changes in second messengers produced by the modulation of an endogenous yeast signaling pathway. For example, changes in intracellular Ca+2, phophorylation states of proteins, activities of intracellular enzymes, and the like can be detected. Still other detection techniques include micorphysiometric devices which permit detection of small changes in, e.g., ions or intracellular pH. In other exemplary embodiments, modulation of, e.g., adenylyl cyclase, cyclic GMP, phosphodiesterases, phosphoinositidases, phosphoinositol kinases, and phospholipases, as well as a variety of ions can be assayed.
In one embodiment, the GTPase enzymatic activity by G proteins can be measured in plasma membrane preparations by determining the breakdown of y32P
GTP
using techniques that are known in the art (For example, see Signal Transduction: A
Practical Approach. G. Milligan, Ed. Oxford University Press, Oxford England).
When receptors that modulate cAMP are tested, it will be possible to use standard techniques for cAMP detection, such as competitive assays which quantitate [3H]CAMP
in the presence of unlabelled cAMP.
Certain receptors and ion channels stimulate the activity of phospholipase C
which stimulates the breakdown of phosphatidylinositol 4,5, bisphosphate to 1,4,5-IP3 (which mobilizes intracellular Ca++) and diacylglycerol (DAG) (which activates protein kinase C). Inositol lipids can be extracted and analyzed using standard lipid extraction techniques. DAG can also be measured using thin-layer chromatography. Water soluble derivatives of all three inositol lipids (IPI, IP2, IP3) can also be quantitated using radiolabelling techniques or HPLC.
The other product of PIP2 breakdown, DAG can also be produced from phosphatidyl choline. The breakdown of this phospholipid in response to receptor-mediated signaling can also be measured using a variety of radiolabelling techniques.
The activation of phospholipase A2 can easily be quantitated using known techniques, including, for example, the generation of arachadonate in the cell.
In other embodiments, e.g., in the case of certain receptors and ion channels, it may be desirable to screen for changes in cellular phosphorylation. Such assay formats may be useful when the receptor of interest is a receptor kinase or phosphatase. For example, immunoblotting (Lyons and Nelson ( 1984) Proc. Natl. Acad. Sci. USA
81:7426-7430) using anti-phosphotyrosine, anti-phosphoserine or anti-phosphothreonine antibodies. In addition, tests for phosphorylation could be also useful when the receptor itself may not be a kinase, but activates protein kinases or phosphatase that function downstream in the signal transduction pathway.
One such cascade is the MAP kinase pathway that appears to mediate both mitogenic, differentiation and stress responses in different cell types.
Stimulation of growth factor receptors results in Ras activation followed by the sequential activation of c-Raf, MEK, and p44 and p42 MAP kinases (ERK 1 and ERK2). Activated MAP kinase then phosphorylates many key regulatory proteins, including p90RSK and Elk-I
that are phosphorylated when MAP kinase translocates to the nucleus. Homologous pathways exist in mammalian and yeast cells. For instance, an essential part of the S.
cerevisiae pheromone signaling pathway is comprised of a protein kinase cascade composed of the products of the STEI l, STE7, and FUS3/KSS1 senes (the latter pair are distinct and functionally redundant). Accordingly, phosphorylation and/or activation of members of this kinase cascade can be detected and used to quantitate receptor engagement.
Phosphotyrosine specific antibodies are available to measure increases in tyrosine phosphorylation and phospho-specific antibodies are commercially available (New England Biolabs, Beverly, MA).
In still other embodiments, the detectable signal can be produced by use of enzymes or chromogenic/fluorescent probes whose activities are dependent on the concentration of a second messenger, e.g., such as calcium, hydrolysis products of inositol phosphate, cAMP, etc. For example , the mobilization of intracellular calcium or the influx of calcium from outside the cell can be measured using standard techniques. The choice of the appropriate calcium indicator, fluorescent, bioluminescent, metallochromic, or Ca++-sensitive microelectrodes depends on the cell type and the magnitude and time constant of the event under study (Borle ( 1990) Environ Health Perspect 84:45-56). As an exemplary method of Ca++ detection, cells could be loaded with the Ca++sensitive fluorescent dye fura-2 or indo-I, using standard methods, and any change in Ca++ measured using a fluorometer.
Detection of Transcription or Transcription Products In addition to directly measuring second messenger production, the signal transduction activity of a receptor can be measured by detection of a transcription product, e.g., by detecting receptor/channel-mediated transcriptional activation (or repression) of an endogenous gene(s). Detection of the transcription product includes detecting the gene transcript, detecting the product directly (e.g., by immunoassay) or detecting an activity of the protein (e.g., such as an enzymatic activity or chromogenic/fluorogenic activity); each of which is generally referred to herein as a means for detecting expression of the indicator gene. The indicator gene may be an unmodified endogenous gene of the yeast cell or a modified endogenous gene.
In one embodiment, the indicator gene is an unmodified endogenous gene. For example, the instant method can rely on detecting the transcriptional level of such pheromone system pathway responsive endogenous genes as the Barl or Fusl, Fus 2, mating factor, Ste3 Stel3, Kexl, Ste2, Ste6, Ste7, sSst2, or Chsl. (Appletauer and Zchstetter. 1989. Eur. J. Biochem. 181:243) In other embodiments, the sensitivity of an endogenous indicator gene can be enhanced by manipulating the promoter sequence at the natural locus for the indicator gene. Such manipulation may range from point mutations to the endogenous regulatory elements to gross replacement of all or substantial portions of the regulatory elements.
The previous discussion of mutations with regard to G proteins and G protein coupled receptors is reiterated here.
For example, in the case of the Barl gene, the promoter of the gene can be modified to enhance the transcription of Barl upon activation of the yeast pheromone system pathway. Barl gene transcription is iactivated upon exposure of yeast cells to mating factor. The sequence of the Barl gene is known in the art (see e.g., U.S. patent 4,613,572). Moreover, the sequences required for a,-factor-enhanced expression of the Barl, and other pheromone responsive genes have been identified. (Appeltauer and Achstetter 1989. Eur. J. Biochem. 181:243; Hagen et al. 1991. Mol. Cell. BioI.
11:2952). In an exemplary embodiment, the yeast Barl promoter can be engineered by mutagenesis to be more responsive, e.g., to more strongly promoter gene transcription, upon stimulation of the yeast pheromone pathway. Standard techniques for mutagenizing the promoter can be used. In such embodiments, it is desirable that the conserved oligonucleotide motif described by Appeltaure et al. be conserved.
In another embodiment, the endogenous Barl promoter of a yeast cell can be replaced, e.g., by homologous recombination, with a Barl promoter engineered to cause higher levels of expression of Barl upon pheromone stimulation.
In another exemplary embodiment, the promoter (or other transcriptional regulatory sequences) of the endogenous gene can be "switched out" with a heterologous promoter sequence, e.g., to form a chimeric gene at the indicator endogenous gene locus.
Again, using such techniques as homologous recombination, the regulatory sequence can be so altered at the genomic locus of the indicator gene. For example, the Barl promoter can be replaced, at the Barl locus, with the promoter for the_fusl (or fus2) gene. The,fusl promoter has a higher responsiveness to stimulation by pheromone induction than the Barl promoter and, accordingly can increase the signal-to-noise and dynamic range of the indicator gene. For example, the fusl and fus2 have been substituted for promoters at other loci, such as for the carol promotor. These strains become canavanine sensitive upon expression of the canl gene. A similar approach was used to introduce the full and fus2 promoter upstream of the ura3 gene in place of the ura3 promoter, thus conferring uracil prototrophy in a manner dependent on activation of the yeast pheromone signal pathway. Likewise, the fusl and fus2 promoter regions can be introduced upstream of other genes in order to control their expresion:
gal l (confering deoxygalactose sensitivity or galactose sensitivity due to the concomitant loss of the gal 10 gene); (3-D-glucanase (exgl: an easily assayed extracellular enzyme);
chitinase (ctsl ); asparaginase (ast3: hydrolyzes asparagine to ammonia and aspartate);
and invertase (suc2); secreted acid phosphatase (pho3 or pho5).
In certain embodiments, it may be desirable to increase the level of transcriptional activation of the endogenous indicator gene by the signal pathway in order to, for example, improve the signal-to-noise of the test system, or to adjust the level of response to a level suitable for a particular detection technique. In one embodiment, the transcriptional activation ability of the signal pathway can be amplified by the overexpression of one or more of the proteins involved in the intracellular signal cascade, particularly enzymes involved in the pathway. For example, increased expression of Jun kinases (JNKs) can potentiate the level of transcriptional activation by a signal in an MEKK/JNKK pathway. Likewise, overexpression of one or more signal transduction proteins in the yeast pheromone pathway can increase the level of Fusl, Fus 2 and/or Barl expression. This approach can also be used to potentiate the level of transcription of a heterologous reporter gene (described below) as well.
Enzyme Activation In yet other embodiments, rather than measuring second messenger production or alterations in transcription, the activity of endogenous yeast proteins can be assayed.
For example, in one embodiment, the signal transduction pathway of the receptor upregulates expression or otherwise activates an enzyme which is capable of modifying a substrate which can be added to the cell. The signal can be detected by using a detectable substrate, in which case loss of the substrate signal is monitored, or alternatively, by using a substrate which produces a detectable product. In certain embodiments, the substrate is naturally occurring. Alternatively, the substrate can be non-naturally occurring.
In a preferred embodiment, the enzyme which cleaves the substrate peptide is the product of the BAR/ gene, the expression of which is upregulated by stimulation of the yeast pheromone pathway. Thus, yeast cells which have been generated to exploit the pheromone signal pathway for detection can be contacted with a suitable detection means, i.e., a substrate peptide which can be cleaved by BAR1 to release a detectable fragment, e.g. a detectably labeled fragment, and the level of BAR1 activity thus determined.
Alterations in enzyme activity mediated by the interaction of a test compound and a receptor can be detected by a number of means. In preferred embodiments, the conversion of the substrate is measured using a semi-quantitative plate assay to measure BARIp activity as described in Example 2. As an illustrative embodiment, cells which lack endogenous BAR1 (referred to as a "test yeast strain") can be grown in an appropriate medium. The overnight cultures can then be poured onto medium containing a-factor, allowed to stand a few minutes and poured off. This results in the formation of a confluent and even lawn of test cells. Since the plated lawn of cells lacks the BAR/ gene, it is super-sensitive to a.-factor causing its growth to be arrested on the a, -factor plate. Medium from Barl-induclibe yeast cells, which have been exposed to test compounds, can be tested for its ability to allow growth of the Barl deficient test yeast cells in the lawn. Growth of the lawn of cells indicates that BAR/ is present in the medium and, therefore, that the pheromone system of the Barl-inducible yeast cell has been modulated by contact with the test compound. Using this assay 2-fold differences in BAR1 activity over a 100-fold concentration range can be distinguished.
In more preferred embodiments, the conversion of the substrate to product by the enzyme produces a detectable change in optical characteristics of the test cell, e.g., the substrate and/or product is chromogenically or fluorogenically active. In an illustrative embodiment the signal transduction pathway causes a change in the activity of a proteolytic enzyme, altering the rate at which it cleaves a substrate peptide (or simply activates the enzyme towards the substrate). The substrate peptide can include a fluorogenic donor radical, e.g., a fluorescence emitting radical, and an acceptor radical, e.g., an aromatic radical which absorbs the fluorescence energy of the fluorogenic donor radical when the acceptor radical and the fluorogenic donor radical are covalently held in close proximity. See, for example, USSN 5,527,681, 5,506,11 S, 5,429,766, 5,424,186, and 5,316,691; and Capobianco et al. (1992) Anal Biochem 204:96-102. For example, the substrate peptide has a fluorescence donor group such as 1-aminobenzoic acid (anthranilic acid or ABZ) or aminomethylcoumarin (AMC) located at one position on the peptide and a fluorescence quencher group, such as Lucifer yellow, methyl red or nitrobenzo-2-oxo-1,3-diazole (NBD), at a different position near the distal end of the peptide. A cleavage site for the activated enzyme will be disposed between each of the sites for the donor and acceptor groups. The intramolecular resonance energy transfer from the fluorescence donor molecule to the quencher will quench the fluorescence of the donor molecule when the two are sufficiently proximate in space, e:g., when the peptide is intact. Upon cleavage of the peptide, however, the quencher is separated from the donor group, leaving behind a fluorescent fragment. Thus, activation of the enzyme results in cleavage of the detection peptide, and dequenching of the fluorescent group.
In a preferred embodiment the substrate used to assay for BAR1 activity is conjugated to a fluorescent donor, such as, S-[(2-aminoethyl)amino]naphthalene-1-sulfonic acid (EDANS), and a quenching acceptor, such as 4-(4-dimethylaminophenylazo)benzoic acid (DABCYL). In a preferred embodiment, the substrate consists of an peptide containing the BARIp recognition sequence with a (EDANS), and (DABCYL), attached at the COOH- and NH2-termini, respectively. In another embodiment the substrate further comprises a GABA group between the EDANS group and the first amino acid at the COOH terminus (e.g., the Trp residue). The intrinsic fluorescence of EDANS
is expected to be dramatically reduced in this substrate because of intramolecular fluorescence resonance energy transfer (FRET) to the DABCYL group. Since FRET
becomes insignificant beyond distances of 100 A, the fluorescence of EDANS is restored after cleavage of the substrate (Matayoshi et al, Science, 1990 247:954). Thus, proteolytic activity can be continuously monitored by recording the increase in fluorescence intensity with time.
Alternatively, a benzamidine, benzyloxycarbonyl (Cbz) group can be attached at the N-terminus of the substrate and a Rhodamine group at the C terminus of the substrate. Free Rhodamine or mono-substituted Rhodamine exists primarily as a highly fluorescent quinone. However, bis-substituted Rhodamine exists as a virtually non-fluorescent lactone (McGrath et al, Virology, 1996 217:131 ). Thus, the bis-substituted BARIp substrate has very little fluorescence. The peptides on the substrate are protected from cleavage by aminopeptidases. Cleavage ofthe peptide with BARIp, renders the residual Rhodamine-attached peptide susceptible to aminopeptidase cleavage.
Aminopeptidase removal of the peptide from Rhodamine will result in production of highly fluorescent mono-substituted and free Rhodamine molecules.
In one embodiment, the substrate to be assayed is naturally occurring yeast a-factor. In a preferred embodiment a substrate comprises the compound:
DABCYL-Trp-Leu-Gln-Leu-Lys-Pro-Gly-Gln-Pro-Met-Tyr- EDANS (SEQ ID
N0:4) In yet another embodiment a preferred substrate comprises the compound:
Cbz-Trp-Leu-Gln-Leu-Lys-Pro-Gly-Gln-Pro-Met-Tyr-NH2-Rhodamine (SEQ
ID NO:S).
Zymogen activation In an additional embodiment, Barl activity can be measured by detecting the activation of an enzyme precursor to an active enzyme. Zymogens are enzyme precursors which become active upon specific, limited proteolytic treatment.
In making a zymogen substrate for use in the instant assays, a Barl sensitive site (e.g.
the sequence of approx. 9-10 amino acids from yeast alpha factor including the Leu-Lys sequence) is introduced between the precursor pro-region of a zymogen and the mature (active) protein sequence by standard genetic engineering techniques. Treatment of the zymogen with Barlp then releases active enzyme from the zymogen. Using this method of detection, yeast cells, or supernatants from yeast cells, which have been stimulated by a compound to produce Barl can be tested by measuring the conversion of zymogen to active enzyme, e.g., by detecting cleavage of a substrate which is sensitive to cleavage by the active enzyme. Examples of zymogens which may be useful in such assays include trypsinogen, plasminogen, prothrombin, pepsinogen, fibrinogen and yeast carboxypeptidase Y and methods of assaying for the activity of the active enzymes derived from these zymogens are well known in the art.
The above system can also be adapted for intracellular zymogen processing. In an exemplary embodiment, the Barl protease may be expressed cytoplasmically by excision of the sequences necessary for secretion from the gene resulting in intracellular expression of the mature Barl protein. Cells expressing this intracellular Barlp are then engineered to coexpress an intracellular zymogen with a Barlp sensitive cleavage and activation site as described above.
To detect Barlp activity, i.e., conversion of the zymogen to active enzyme, several assays can be used. For example, the bacterial Lac alpha fragment can be fused with a large peptide or a protein. Such a fusion renders Lac alpha incapable of complementation with the Lac omega fragment. (This complementation is the basis of the blue-white discrimination of in frame insertion clones in Lac alpha vectors).
However, if such a Barl sensitive site is included proximal to the Lac alpha-peptide fusion junction, treatment with Barl p will release the functional Lac alpha peptide which is now capable of Lac alpha-omega complementation. Thus, Barl activity can be read out as a color change in the cell. Beta galactosidase enzyme activity can be detected and measured by any of a wealth of commonly used methods, the most preferred being a chromogenic assay based on indigo dye formation on treatment of the X-gal substrate. In another embodiment, this system may be incorporated into the zymogen embodiment above, allowing both beta-galactosidase and zymogen readouts.
Substrate Stability In yet another embodiment of an assay which is based on the detection of modulation of enzyme activity, an enzyme substrate may be modified such that cleavage by the enzyme results in destabilization of the substrate (an example of which is described further in Example 5}. For example, proteins with Lys at their N-terminus are unstable in yeast (Bachmair and Varshavsky. 1989. Cell. 56:1019). Accordingly, an enzyme substrate which will be cleaved to expose an N-terminal Lys can be fused to an easily assayed detection protein. For instance, the BAR1 substrate, a-factor, can be fused to a detectable gene, e.g. a lacZ gene. In preferred embodiments, it may be desirable to modify the endogenous BARI gene, to remove signals for secretion (present at the N and C-terminus of BARD, thereby enhancing interaction of BAR1 with cytoplasmic substrates. In certain embodiments, the detection protein is an essential protein, thus providing negative selection for BAR1 expression or activity. In other embodiments, a repressor protein can be used as the detection protein, thereby providing a positive readout.
The Use of Chimeric Constructs to Make Endogenous Genes Pheromone Responsive In yet another embodiment chimeric constructs can be used confer pheromone-responsiveness on endogenous yeast genes that are not normally pheromone-responsive as described in Example 6. Such constructs comprise a segment of a gene encoding a pheromone inducible transcription factor, such as the Stel2p transcription factor. For example, in the presence of pheromone signaling, Stel2p becomes a potent transcriptional activator of genes whose promoters contain a well-defined DNA
binding site (the pheromone response element, or PRE). The chimericconstructs further comprise a second segment, encoding a DNA binding domain that binds a DNA
sequence in the promoter of the endogenous gene on which pheromone responsiveness is to be conferred. The gene from which the second segment is derived will be selected based on the desired readout. For example, if the assay is to be constructed using gene A as the readout (because of the ease of assaying for the product of gene A), then the second segment of the chimeric construct encodes a DNA binding domain which binds to the gene A promoter and induces expression of gene A which is to be assayed. For example, in a preferred embodiment, the second segment of the construct encodes the DNA binding domain of Pho4p. Wild-type Pho4p binds and activates the promoter of the PH05, a secreted alkaline phosphatase gene. Upon expression of the chimeric construct, signaling through the pheromone response pathway will activate the Pho4-Stel2 fusion protein encoded by the chimeric construct, and then this Pho4-Stel2 fusion protein will bind to the Pho4 binding site in the PhoS promoter and induce expression of the PHOS gene.
In assays employing chimeric constructs, the modulation of a receptor by a test compound will result in a change in the transcription of a gene, which is not normally pheromone responsive. In preferred embodiments, the gene is easily detectable.
For example, in a preferred embodiment, the subject assay can be used to measure PhoS, a secreted acid phosphatase. Acid phosphatase activity can be measured using standard techniques. For example, the overlay assay of Toh-a et al (J. Bacteriol, 1973) can be used. For example, cells are patched onto the appropriate medium and allowed to grow overnight. For each plate, a mixture of 2 ml of molten 1 % agarose in 50 mM
NaAc pH
4.0, 700 p.1 H20, and 300 p1 a.-napthyl acid phosphate (50 mg/ml) is prepared and applied to the plate. Then lml of D-dianisidine fast blue salt B (SOmg/ml in 50 mM
NaAc pH 4.0) is poured onto the plate. The degree of color development is a measure of the level of acid phosphatase produced by the patch of cells. Such color development is indicative of the modulation of a receptor by a test compound.
In certain embodiments, such chimeric constructs will further comprise a nuclear localization sequence.
As indicated above, in preferred embodiments the DNA binding domain of the construct (i.e., encoded by the second segment of the construct) from the PHO=l DNA
binding domain. The sequence of the PH04 DNA binding domain is known in the art.
The construct can comprise a segment of the naturally occurring PH04 gene, or can comprise a segment which is derived from the naturally occurring PH04 gene, but which has been altered, e.g., by mutation. In preferred embodiments, the second gene segment encodes amino acids 227-312 of the PH04 DNA binding domain.
In other preferred embodiments the pheromone-inducible transcription factor (i.e., encoded by the first gene segment of the construct) is derived from the Stel2 gene.
Any of a number of Stel2 fragments can be used in the subject constructs. The sequence of Sie 12 is known in the art. There are several sources of information regarding the sequence of Stel2 that the skilled artisan can refer to when selecting the segment of Ste 12 to incorporate into the chimeric construct. For example, fusions have been made between the Gal4 DNA binding domain and different regions of Ste 12 (Song et al Genes c& Development, 1991 ). Additionally, deletion and insertion mutants of Stel2 have been constructed and tested for their ability to restore mating and transcriptional activity to a ste120 strain (Kirkman-Correia et al Mol Cell Biol, 1993).
Such experiments provide guidance as to portions of Stel2 which can be incorporated into the constructs and which portions are likely to be amenable to mutation.
The chimeric constructs of the instant invention can comprise a segment derived from a naturally DNA sequence, or the subject constructs can comprise a segment which is homologous to a naturally occurring gene, but which has been altered, e.g., by mutation. Any of the standard methods of making mutations which are known in the art or discussed herein can be used for this purpose.
For example, in preferred embodiments, the first gene segment which is incorporated into the construct comprises a nucleotide sequence which encodes amino acids 1-473 of the naturally occurring Stel2. In another embodiment, the construct comprises a nucleotide sequence which encodes amino acids 214-473 of naturally occurring Stel2. In another embodiment, the construct comprises a nucleotide sequence encoding amino acids 214-688 of naturally occurring Ste 12. In yet another embodiment, the construct comprises a nucleotide sequence encoding amino acids of naturally occurring Stel2.
In yet other embodiments, the segment of the construct derived from the Ste 12 gene can comprise a mutation. For example, in one embodiment, such a mutation can result in the insertion of one or more amino acids, e.g., the insertion of Lys-Leu between amino acids 85 and 86 of Ste 12. In another embodiment, such a mutation can result in an insertion of Ser-Leu between amino acids 103 and 104. In yet another embodiment one or more amino acids can be deleted, for example, amino acids 253-305, 572-669, or 588-669.
In preferred embodiments, the endogenous yeast gene which corresponds to a gene present in the construct is disrupted. For example, in preferred embodiments, yeast cells bearing a Ste 12-PH04 construct can be engineered such that the PH04 gene of the host yeast cell can be disrupted. In other preferred embodiments, the PH03 gene, which also encodes a secreted acid phosphatase, but which is induced under high-phosphate conditions and is further increased by thiamine starvation, can be disrupted.
Heterologous Readouts: Reporter Gene Constructs In yet other embodiments, a heterologous gene construct can be used to detect the modulation of a receptor. By selecting transcriptional regulatory sequences that are responsive to the transduced intracellular signals and operatively linking the selected promoters to reporter genes, whose transcription or translation is readily detectable and measurable, a transcription based assay provides a rapid indication of whether a specific receptor interacts with a test compound in any way that modulates intracellular transduction. Expression of the reporter gene, thus, provides a valuable screening tool for the development of compounds that act as agonists or antagonists of such a receptor.
Reporter gene based assays of this invention measure the end stage of the above described cascade of events, e.g., transcriptional modulation. Accordingly, in practicing one embodiment of the assay, a reporter gene construct is inserted into the reagent cell in order to generate a detection signal dependent on receptor signaling.
Typically, the reporter gene construct will include a reporter gene in operative linkage with one or more transcriptional regulatory elements responsive to the signal transduction activity of the target receptor, with the level of expression of the reporter gene providing the receptor-dependent detection signal. In either embodiment, the amount of transcription from the indicator gene may be measured using any method known to those of skill in the art to be suitable.
In preferred embodiments, the product of the reporter gene is detected by an intrinsic activity associated with that product. For instance, the indicator gene may encode a gene product that, by enzymatic activity, gives rise to a detection signal based on, for example, color, fluorescence, or luminescence.
The amount of expression from the reporter gene is then compared to the amount of expression in either the same cell in the absence of the test compound or it may be compared with the amount of transcription in a substantially identical cell that lacks the specific receptors. A control cell may be derived from the same cells from which the test cell was prepared but which had not been treated with the compound.
Alternatively, it may be a cell in which the receptor of interest is not present. Any change in the amount of transcription (e.g., a statistically significant change) indicates that the test compound has in some manner altered the activity of the specific receptor or ion channel.
In other preferred embodiments, the reporter gene provides a selection method such that cells in which activation (or inactivation) of one or more signal pathways of a receptor or ion channel provides a growth advantage to the treated cell. For example, expression of the indicator gene could enhance cell viability, relieve a cell nutritional requirement, and/or provide resistance to a drug.
Many exemplary reporter genes and transcriptional regulatory elements are known to those of skill in the art and others may be identified or synthesized by methods known to those of skill in the art. Such examples of reporter genes include, but are not limited to CAT (chloramphenicol acetyl transferase) (Alton and Vapnek (1979), Nature 282: 864-869) luciferase, and other enzyme detection systems, such as beta-galactosidase; firefly luciferase (deWet et al. (1987), Mol. Cell. Biol. 7:725-737);
bacterial luciferase (Engebrecht and Silverman (1984), PNAS l: 4154-4158;
Baldwin et al. (1984), Biochemistry 23: 3663-3667); alkaline phosphatase (Toh et al.
(1989) Eur. J.
Biochem. 182: 231-238, Hall et al. (1983) J. Mol. AppI. Gen. 2: 101), human placental secreted alkaline phosphatase (Cullen and Malim (1992) Methods in Enzymol.
216:362-368); (3-lactamase or GST.
Transcriptional control elements for use in the reporter gene constructs, or for modifying the genomic locus of an indicator gene include, but are not limited to, promoters, enhancers, and repressor and activator binding sites. Suitable transcriptional regulatory elements may be derived from the transcriptional regulatory regions of genes whose expression is rapidly induced, generally within minutes, of contact between the cell surface protein and the effector protein that modulates the activity of the cell surface protein. Examples of such genes include, but are not limited to, the immediate early genes (see, Sheng et al. (1990) Neuron 4: 477-485), such as c-fos. Immediate early genes are genes that are rapidly induced upon binding of a ligand to a cell surface protein. The transcriptional control elements that are preferred for use in the gene constructs include transcriptional control elements from immediate early genes, elements derived from other genes that exhibit some or all of the characteristics of the immediate early genes, or synthetic elements that are constructed such that genes in operative linkage therewith exhibit such characteristics. The characteristics of preferred genes from which the transcriptional control elements are derived include, but are not limited to, low or undetectable expression in quiescent cells, rapid induction at the transcriptional level within minutes of extracellular simulation, induction that is transient and independent of new protein synthesis, subsequent shut-off of transcription requires new protein synthesis, and mRNAs transcribed from these genes have a short half life. It is not necessary for all of these properties to be present.
Other promoters and transcriptional control elements, in addition to those described above, include the vasoactive intestinal peptide (VIP) gene promoter (CAMP
responsive; Fink et al. (1988), Proc. Natl. Acad. Sci. 85:6662-6666); the somatostatin gene promoter (CAMP responsive; Montminy et al. ( 1986), Proc. Natl. Acad.
Sci.
8.3:6682-6686); the proenkephalin promoter (responsive to cAMP, nicotinic agonists, and phorbol esters; Comb et al. (1986), Nature 323:353-356); the phosphoenolpyruvate carboxy-kinase gene promoter (CAMP responsive; Short et al. ( 1986), J. Biol.
Chern.
261:9721-9726); the NGFI-A gene promoter (responsive to NGF, cAMP, and serum;
Changelian et al. (1989). Proc. Natl. Acad. Sci. 86:377-381); and others that may be known to or prepared by those of skill in the art.
In the case of receptors which modulate cyclic AMP, a transcriptional based readout can be constructed using the cyclic AMP response element binding protein, CREB, which is a transcription factor whose activity is regulated by phosphorylation at a particular serine (5133). When this serine residue is phosphorylated, CREB
binds to a recognition sequence known as a CRE (CAMP Responsive Element) found to the 5' of promotors known to be responsive to elevated cAMP levels. Upon binding of phosphorylated CREB to a CRE, transcription from this promoter is increased.
Phosphorylation of CREB is seen in response to both increased cAMP levels and increased intracellular Ca levels. Increased cAMP levels result in activation of PKA, which in turn phosphorylates CREB and leads to binding to CRE and transcriptional activation. Increased intracellular calcium levels results in activation of calcium/calmodulin responsive kinase II (CaM kinase II). Phosphorylation of CREB by CaM kinase II is effectively the same as phosphorylation of CREB by PKA, and results in transcriptional activation of CRE containing promotors.
A transcriptionally-based readout can be constructed in cells containing a reporter gene whose expression is driven by a basal promoter containing one or more CRE. Changes in the intracellular concentration of Ca++ (a result of alterations in the activity of the receptor upon engagement with a ligand) will result in changes in the level of expression of the reporter gene if: a) CREB is also co-expressed in the cell, and b) either an endogenous or heterologous CaM kinase phosphorylates CREB in response to increases in calcium or if an exogenously expressed CaM kinase II is present in the same cell. In other words, stimulation of PLC activity may result in phosphorylation of CREB and increased transcription from the CRE-construct, while inhibition of PLC
activity may result in decreased transcription from the CRE-responsive construct.
As described in Bonni et al. (1993) Science 262:1575-1579, the observation that CNTF treatment of SK-N-MC cells leads to the enhanced interaction of STAT/p91 and STAT related proteins with specific DNA sequences suggested that these proteins might be key regulators of changes in gene expression that are triggered by CNTF.
Consistent with this possibility is the finding that DNA sequence elements similar to the consensus DNA sequence required for STAT/p91 binding are present upstream of a number of genes previously found to be induced by CNTF (e.g., Human c-fos, Mouse c-fos, Mouse tisl l, Rat junB, Rat SOD-1, and CNTF). Those authors demonstrated the ability of STAT/p91 binding sites to confer CNTF responsiveness to a non-responsive reporter gene. Accordingly, a reporter construct for use in the present invention for detecting signal transduction through STAT proteins, such as from cytokine receptors, can be generated by using -71 to +109 of the mouse c-fos gene fused to the bacterial chloramphenicol acetyltransferase gene (-71 fosCAT) or other detectable reporter gene.
Induction by a cytokine receptor induces the tyrosine phosphorylation of STAT
and STAT-related proteins, with subsequent translocation and binding of these proteins to the STAT-RE. This then leads to activation of transcription of genes containing this DNA element within their promoters.
In preferred embodiments, the reporter gene is a gene whose expression causes a phenotypic change which is screenable or selectable. If the change is selectable, the phenotypic change creates a difference in the growth or survival rate between cells which express the reporter gene and those which do not. If the change is screenable, the phenotype change creates a difference in some detectable characteristic of the cells, by which the cells which express the reporter may be distinguished from those which do not. Selection is preferable to screening in that it can provide a means for amplifying from the cell culture those cells which express a test polypeptide which is a receptor effector.
The reporter gene is coupled to the receptor signaling pathway so that expression of the reporter gene is dependent on activation of the receptor. This coupling may be achieved by operably linking the reporter gene to a receptor-responsive promoter. The term "receptor-responsive promoter" indicates a promoter which is regulated by some product of the receptor's signal transduction pathway.
Alternatively, the promoter may be one which is repressed by the receptor pathway, thereby preventing expression of a product which is deleterious to the cell.
With a receptor repressed promoter, one screens for agonists by linking the promoter to a deleterious gene, and for antagonists, by linking it to a beneficial gene.
Repression may be achieved by operably linking a receptor- induced promoter to a gene encoding mRNA which is antisense to at least a portion of the mRNA encoded by the reporter gene (whether in the coding or flanking regions), so as to inhibit translation of that mRNA. Repression may also be obtained by linking a receptor-induced promoter to a gene encoding a DNA binding repressor protein, and incorporating a suitable operator site into the promoter or other suitable region of the reporter gene.
In the case of yeast, suitable positively selectable (beneficial) genes include the following: URA3, LYS2, HISS, LEU2, TRPI ; ADEI, 2, 3, 4, 5, 7, 8; ARGI, 3, 4, 5, 6, 8;
HISl , ~, 5; IL VI , 2, 5; THR I , ~t; TRP2, 3, 4, 5; LEUI , ;t; MET2, 3, 4, 8, 9, I 4,16,19;
URA 1, 2, 4, 5,10; HOM3, 6; ASPS; CHOI ; ARO 2, 7; CYS3; OLEI ; INDI , 2, 4;
PROl , 3 Countless other genes are potential selective markers. The above are involved in well-characterized biosynthetic pathways. The imidazoleglycerol phosphate dehydratase (IGP dehydratase) gene (HIS3) is preferred because it is both quite sensitive and can be selected over a broad range of expression levels. In the simplest case, the cell is auxotrophic for histidine (requires histidine for growth) in the absence of activation.
Activation leads to synthesis of the enzyme and the cell becomes prototrophic for histidine (does not require histidine). Thus the selection is for growth in the absence of histidine. Since only a few molecules per cell of IGP dehydratase are required for histidine prototrophy, the assay is very sensitive.
In a more complex version of the assay, cells can be selected for resistance to aminotriazole (AT), a drug that inhibits the activity of IGP dehydratase.
Cells with low, fixed level of expression of HIS3 are sensitive to the drug, while cells with higher levels are resistant. The amount of AT can be selected to inhibit cells with a basal level of HIS3 expression (whatever that level is) but allow growth of cells with an induced level of expression. In this case selection is for growth in the absence of histidine and in the presence of a suitable level of AT.
In appropriate assays, so-called counterselectable or negatively selectable genes may be used. Suitable genes include: URA3 (orotidine-5'-phosphate decarboxylase;
inhibits growth on 5-fluoroorotic acid), LYS2 (2-aminoadipate reductase;
inhibits growth on a-aminoadipate as sole nitrogen source), CYH2 (encodes ribosomal protein L29; cycloheximide-sensitive allele is dominant to resistant allele), CANI
(encodes arginine permease; null allele confers resistance to the arginine analog canavanin), and other recessive drug-resistant markers.
In one example, the reporter gene effects yeast cell growth. The natural response to signal transduction via the yeast pheromone system response pathway is for cells to undergo growth arrest. This is the preferred way to select for antagonists to a ligand/receptor pair that induces the pathway. An autocrine peptide antagonist would inhibit the activation of the pathway; hence, the cell would be able to grow.
Thus, the FAR1 gene may be considered an endogenous counterselectabIe marker. The FARI
gene is preferably inactivated when screening for agonist activity.
The reporter gene may also be a screenable gene. The screened characteristic may be a change in cell morphology, metabolism or other screenable features.
Suitable markers include beta-galactosidase (Xgal, C 12FDG, Salmon-gal, Magenta-Gal (latter two from Biosynth Ag)), alkaline phosphatase, horseradish peroxidase, exo-glucanase (product of yeast exbl gene; nonessential, secreted); luciferase; bacterial green fluorescent protein; (human placental) secreted alkaline phosphatase (SEAP);
and chloramphenicol transferase (CAT). Some of the above can be engineered so that they are secreted (although not (3-galactosidase). A preferred screenable reporter gene is beta-galactosidase; yeast cells expressing the enzyme convert the colorless substrate Xgal into a blue pigment. Again, the promoter may be receptor-induced or receptor-inhibited.
In certain assays it may be desirable to use changes in growth in the screening procedure. For example, one of the consequences of activation of the pheromone signal pathway in wild-type yeast is growth arrest. If one is testing for an antagonist of a G
protein-coupled receptor, this normal response of growth arrest can be used to select cells in which the pheromone response pathway is inhibited. That is, cells exposed to a test compound will be growth arrested if the compound is an agonist, but will grow normally if the compound is neutral or an antagonist. Thus, the growth arrest response can be used to advantage to discover compounds that function as agonists or antagonists.

Moreover, the effect of growth arrest can provide a selective advantage in the presence of an agent which is cytotoxic to mitotic cells. For example, during the growth arrest window, the cytotoxic agent is added to the culture. Cells which proceed through the cell-cycle, e.g., which are not growth arrested, will be killed. At some time after the addition of the cytotoxic agent, it can be washed from the culture, and surviving cells permitted to proceed with proliferation. Cells which were arrested by the test compound will be enriched in the surviving population.
However, in certain embodiments (particularly those in which an autocrine peptide library is employed), the growth arrest consequent to activation of the pheromone response pathway is an undesirable effect since cells that bind agonists stop growing while surrounding cells that fail to bind peptides will continue to grow. The cells of interest, then, will be overgrown or their detection obscured by the background cells, confounding identification of the compound of interest. To overcome this problem the present invention teaches engineering the cell such that: 1 ) growth arrest does not occur as a result of exogenous signal pathway activation (e.g., by inactivating the FAR1 gene); and/or 2) a selective growth advantage is conferred by activating the pathway (e.g., by transforming an auxotrophic mutant with a HIS3 gene under the control of a pheromone-responsive promoter, and applying selective conditions).
It is desirable that the exogenous receptor be exposed on a continuing basis to the peptides. Unfortunately, this is likely to result in desensitization of the pheromone pathway to the stimulus. For example, the mating signal transduction pathway is known to become desensitized by several mechanisms including pheromone degradation and modification of the function of the receptor, G proteins and/or downstream elements of the pheromone signal transduction by the products of the SST2, STE50, AFR1 (Konopka, J.B. (1993) Mol. Cell. Biol. 13:6876-6888) and SGV1, MSGS, and SIG1 genes. Selected mutations in these genes can lead to hypersensitivity to pheromone and an inability to adapt to the presence of pheromone. For example, introduction of mutations that interfere with function into strains expressing heterologous G
protein-coupled receptors constitutes a significant improvement on wild type strains and enables the development of extremely sensitive bioassays for compounds that interact with the receptors. Other mutations e.g. STE50, sgvl,Barl, ste2,ste3,pikl,msg5, sigh and aftl, have the similar effect of increasing the sensitivity of the bioassay. Thus desensitization may be avoided by mutating (which may include deleting) the SST2 gene so that it no longer produces a functional protein, or by mutating one of the other genes listed above.
If a test compound fails to stimulate the activity of a receptor, the assay may be repeated and modified by the introduction of a step in which the reagent cell is first contacted with a known activator of the target receptor/channel to induce signal transduction, and the test compound can be assayed for its ability to inhibit the activated receptor/channel, e.g., to identify antagonists. In yet other embodiments, batteries of compounds can be screened for agents which potentiate the response to a known activator of the receptor.
X11. Genetic Markers in Yeast Strains Yeast strains that are auxotrophic for histidine (HIS3) are known, see Struhl and Hill, (1987) Mol. Cell. Biol., 7:104; Fasullo and Davis, Mol. Cell. Biol., (1988) 8:4370.
The HIS3 (imidazoleglyceroI phosphate dehydratase) gene has been used as a selective marker in yeast. See Sikorski and Heiter, (1989) Genetics, 122:19; Struhl, et al., P.N.A.S. (1979) 76:1035; and, for FUS1-HIS3 fusions, see Stevenson, et al., (1992) Genes Dev., 6:1293.
Xlll. Pharmaceutical Preparations ofldentified Agents After identifying certain test compounds in the subject assay ,e.g.,as potential surrogate ligands, or receptor antagonists, the practioner of the subject assay will continue to test the efficacy and specificity of the selected compounds both in vitro and in vivo. Whether for subsequent in vivo testing, or for administration to an animal as an approved drug, agents identified in the subject assay can be formulated in pharmaceutical preparations for in vivo administration to an animal, preferably a human.
The compounds selected in the subject assay, or a pharmaceutically acceptable salt thereof, may accordingly be formulated for administration with a biologically acceptable medium, such as water, buffered saline, polyol (for example, glycerol, propylene glycol, liquid polyethylene glycol and the like) or suitable mixtures thereof.
The optimum concentration of the active ingredients) in the chosen medium can be determined empirically, according to procedures well known to medicinal chemists. As used herein, "biologically acceptable medium" includes any and all solvents, dispersion media, and the like which may be appropriate for the desired route of administration of the pharmaceutical preparation. The use of such media for pharmaceutically active substances is known in the art. Except insofar as any conventional media or agent is incompatible with the activity of the compound, its use in the pharmaceutical preparation of the invention is contemplated. Suitable vehicles and their formulation inclusive of other proteins are described, for example, in the book Remington's Pharmaceutical Sciences (Remington's Pharmaceutical Sciences. Mack Publishing Company, Easton, Pa., USA i 985). These vehicles include injectable "deposit formulations". Based on the above, such pharmaceutical formulations include, although not exclusively, solutions or freeze-dried powders of the compound in association with one or more pharmaceutically acceptable vehicles or diluents, and contained in buffered media at a suitable pH and isosmotic with physiological fluids. In preferred embodiment, the compound can be disposed in a sterile preparation for topical and/or systemic administration. In the case of freeze-dried preparations, supporting excipients such as, but not exclusively, mannitol or glycine may be used and appropriate buffered solutions of the desired volume will be provided so as to obtain adequate isotonic buffered solutions of the desired pH. Similar solutions may also be used for the pharmaceutical compositions of compounds in isotonic solu~ons of the desired volume and include, but not exclusively, the use of buffered saline-solutions with phosphate or citrate at suitable concentrations so as to obtain at all times isotonic pharmaceutical preparations of the desired pH, (for example, neutral pH).
Exempl fcation The invention now being generally described will be more readily understood by reference to the following examples, which are included merely for purposes of illustration of certain aspects and embodiments of the present invention and are not intended to limit the invention.
Example 1: Development of Assays for Barl Protease Activity This example describes the development of assays to facilitate the use of the Barl protease as a readout for induction of the pheromone-response pathway in S.
cerevisiae. The S. cerevisiae BARI gene encodes a protease that recognizes and cleaves the yeast a-factor peptide pheromone. Barlp cleaves the mature 13 amino acid a-factor peptide between residues 6 and 7 (Leu-Lys), rendering the pheromone inactive.
Barlp has three features that make it potentially useful as a readout system: (1.) The BARI
gene is induced by signaling through the pheromone-response pathway, (2.) Barlp is secreted, and (3.) Barlp is a catalytic enzyme, allowing signal amplification (Reviewed by Sprague and Thorner in The Molecular and Cellular Biology of the Yeast Scaaharomyces. Vol.2. 1992).

Strain Construction To facilitate development of an assay for Barlp activity, the BART gene was cloned into two yeast expression plasmids. One, a low copy number vector in which the gene is under its own promoter and the other, a high copy number vector in which the gene is driven by the strong constitutive S. cerevisiae PGK promoter. Both plasmids contain the S. cerevisiae LEU2 gene to maintain selection in yeast. The primers:
#1- 5' CTAATCTCGAGTTAAGAAGGCCGTT 3' (SEQ ID NO: l) and #2- 5' GTTAAGGATCCTGTACTCCAGATTT 3' (SEQ ID N0:2) were used to amplify bases -480 to I 760 of the BART gene from yeast genomic DNA.
The amplified product bears an Xhol site at its 5' end, a BamI-I1 site at its 3' end, and contains the complete Barl open reading frame as well as all of the promoter elements known to influence BARI expression (Kronstad et al. Cell. 1987). The product was digested with Xho l and BamH 1 and subcloned into a yeast expression vector (pRS415, referred to herein as Cadus 1014; see e.g., Sikorski and Hieter. 1989.
Genetics. 122:19) that had been digested with Xho 1 and BamH 1. The resulting plasmid was designated Cadus 3974.
To create the PGK-BARI expression plasmid, primer #2 and primer #3- 5' GATATCGTCTCACATGTCTGCAATTA 3' (SEQ ID N0:3) were used to amplify sequences encoding just the BARI open reading frame from the PCR product described above. The product bears a BsmB 1 site (digestion with BsmBI
results in an NcoI compatable overhang) at its 5' and a BamH I site at its 3' end. The product was digested with BsmBl and BamHl and subcloned into Cadus 1651 that had been digested with Ncol and BamHl. The resulting plasmid was designated Cadus 3975.
Cadus 1014, 3974, 1651, and 3975 were introduced into Cadus 579 (MATa Barl: : hisG.': URA3 trpl leu2 ura3 his3 FUSl: : HISS stel ~: : TRPI ), a yeast strain that lacks its own copy of the BARI gene.
Barl Plate Assay A semi-quantitative plate assay was used to measure Barlp activity. Although Barlp from any source can be used in this assay, in this example Barlp produced by CY
11362 (Cadus 579 containing Cadus 397) was used. CY 11362 cells were grown to stauration overnight in SD LEU- medium. The cells were removed from the culture by filtration. The activity of Barl p in the conditioned media was measured. by spotting 2 ~.l onto a Barl assay plate (described below). To determine the sensitivity of the assay, eight two-fold serial dilutions of the conditioned medium were made and 5 ~l of each dilution was applied to the assay plate.
Assay plates were prepared as follows. CY 579 cells were grown overnight in YEPD medium. The overnight cultures were diluted to OD600 0.1 and allowed to grow a few hours (to OD600 0.4). The cells were then diluted to OD600 0.1 in H20 and 5 ml were poured onto a YEPD + a-factor plate (lpg a-factor spread evenly on the surface of a YEPD plate just prior to use), allowed to stand a few minutes and poured off. This results in the formation of a confluent and even lawn of cells on the YEPD + a-factor plate. The conditioned media was then applied to the assay plate and the plate was incubated at 30°C for 1-2 days.
Since CY 579 lacks the BARI gene, it is super-sensitive to a-factor causing its growth to be arrested on the YEPD + a-factor plate. If the conditioned media applied to the lawn contains Barl p activity, the a-factor in that region is destroyed, allowing growth of the CY 579 cells.
Using this assay 2-fold differences in Barl activity over a 100-fold concentration range can be distinguished. Thus, this assay is useful for assessing activation of the pheromone response pathway in cells expressing only the endogenous BARI gene.
The series of serial dilutions of CY 11362 conditioned media described in this example are used to generate a standard curve and thus to provide a semi-quantitative assay for Barlp activity. For this purpose, a large pool of CY 11362 conditioned media was prepared and aliquots were frozen for use in subsequent experiments.
Fluorescent Barl Substrates Two novel fluorescent substrates have been designed to monitor activity of the Barlp protease in liquid assays that are amenable to high-throughput screening. Each of these substrates includes the Barlp peptide-recognition sequence and has been designed such that cleavage by Barl results in a pronounced fluorescence signal. The first substrate, DABCYL-(GABA)- Trp-Leu-Gln-Leu-Lys-Pro-Gly-Gln-Pro-Iviet-Tyr -EDANS (SEQ ID NO: 4) Is based on a substrate for the H1V-1 protease (Matayoshi et al, Science, 1990 supra). The substrate consists of an peptide containing the Barlp recognition sequence with a fluorescent donor, 5-[(2-aminoethyl)amino]naphthalene-1-sulfonic acid (EDANS), and a quenching acceptor, 4-(4-dimethylaminophenylazo)benzoic acid (DABCYL), attached at the COOH- and NH2-termini, respectively. The intrinsic fluorescence of EDANS
is expected to be dramatically reduced in this substrate because of intramolecular fluorescence resonance energy transfer (FRET) to the DABCYL group. Since FRET
becomes insignificant beyond distances of 100 A, the fluorescence of EDANS is -?g-restored after cleavage of the peptide (Matayoshi et al, Science, 1990 supra).
The second substrate, Cbz- Trp-Leu-Gln-Leu-Lys-Pro-Gly-Gln-Pro-Met-Tyr-NH)~ -Rhodamine (SEQ ID IV'O:5) is based on a substrate for the adenovirus proteinase (McGrath et al, Virology, 1996 supra).
Free lthodamine or mono-substituted Rhodamine exists primarily as a highly fluorescent quinone. However, bis-substituted Rhodamine exists as a virtually non-fluorescent lactone (McGrath et al, Virology, 1996 supra). Thus, the bis-substituted Barlp suhstrate exhibits very little fluoresence. This substrate may be used in a coupled assay, which involves cleavage first by Barlp and then by an added amino peptidase. The peptides on the substrate are protected from cleavage by aminopeptidases. Cleavage of the peptide with Barlp, renders the residual Rhodamine-attached peptide susceptible to cleavage by added aminopeptidase. Aminopeptidase removal of the peptide from Rhodamine will result in production of highly fluorescent mono-substituted and free Rhodamine molecules.
Zymogen Activation Assays In an additional embodiment, Barl activity can be measured by assaying the activation of an enzyme precurson to an active enzyme. Zymogens are enzyme precursors which become active upon specific, limited proteolytic treatment. A
Barl sensitive site (e.g. the sequence of approx. 9-10 amino acids from yeast alpha factor including the Leu-Lys sequence) is introduced between the precursor pro-region of a zymogen and the mature (active) protein sequence by standard genetic engineering techniques. Treatment of the zymogen with Barl p then releases active enzyme from the zymogen. Using this method of detection, yeast cells, or supernatants from yeast cells, which have been stimulated by a compound to produce Barl can be tested for thier ability to activate a zymogen. The zymogen activity is then measured by methods well known by those of skill in the art. Examples of zymogens which may be useful in such assays include trypsinogen, plasminogen, prothrambin, pepsinogen, fibrinogen and yeast carboxypeptidase Y.
The above system can also be adapted for intracellular zymogen processing. The Barl protease may be expressed cytoplasmically by excision of the sequences necessary for secretion from the gene resulting in intracellular expression of the mature Barl protein. Cells expressing this intracellular Barlp are engineered to coexpress an intracellular zymogen with a Barlp sensitive cleavage and activation site as described above.

Fusion of the bacterial Lac alpha fragment with a large peptide or a protein renders it incapable of complementation with the Lac omega fragment. (This is the basis of the blue-white discrimination of in frame insertion clones in Lac alpha vectors).
However, if such a fusion of Lac alpha with another peptide or protein has a Barl sensitive site proximal to the fusion junction such that treatment with Barlp releases a functional Lac alpha peptide which is now capable of Lac alpha-omega complementation. Beta galactosidase enzyme activity can be detected and measured by any of a wealth of commonly used methods, the most preferred being a chromogenic assay based on indigo dye formation on treatment of the X-gal substrate. This system may be incorporated into the zymogen embodiment above, allowing both beta-galactosidase and zymogen readouts.
Example 2: Detection of Ste2p Activation using the Barl Plate Assay This example demonstrates the utility of the Barl plate assay for assessing agonist-induced activation of the S. cerevisiae pheromone receptor, Ste2p.
Strain Construction First, the gene encoding the S. cerevisiae Ga, GPA1, was reintroduced into the genome of CY 8034 (MATa gpal *1162 ,Earl-I stet*IIS;t stel-l::trpl::LYS2 fusl-HIS3 ura3 trpl leu2 lys2 his3 ade2-I metl ) by transformation with an integrating plasmid encoding GPAI (Cadus 3907), creating CY 11364. Next, the gene encoding the S. cerevisiae RGS protein, SST2, was disrupted in this strain to create CY
11645. Since Sst2p is involved in desensitization of the pheromone response pathway, its disruption results in increased signaling through the pathway (Reviewed by Sprague and Thorner in Molecular and Cellular Biology of the Yeast Saccharomyces. Vol. 2. 1992).
A high copy number Ste2 expression plasmid was constructed as follows. The 4.3 kb BamHl fragment containing the entire STE2 gene was excised from the yeast expression plasmid Yep24-STE2 (obtained from J. Thorner, Univ. of California Berkeley) and cloned into the BamHl site of pRS425 (Cadus 1018) (Sikorski and Heiter, Genetics. 1989). The resulting plasmid, Cadus 2456, and the vecotr control, Cadus 1018, were then introduced into CY 1 I 645 to create CY 11728 and CY
11727, respectively.
Detection of Ste2p Activation Using the Barl Plate Assay Overnight cultures of CY 11727 and CY 11728 were diluted in SD LEU-medium to an OD6pp of 0.2 and allowed to grow for a few hours at 30°C
(to OD600 0.4). The cells were collected by centrifugation, washed 1 X with SD LEU-medium, and resuspended in 2 ml SD LEU- medium. The cultures were split in half and a,-factor ( 10 p,g) was added to one aliquot and vehicle (in this case, H20) was added to the other.
After 2 hours of incubation at 30°C, the cells were removed either by four successive rounds of centrifugation or by filtration, and 5 p1 of the conditioned media was applied to a Barl assay plate (described in Example 1). A standard curve was also done with each experiment (described in Example 1 ) to quantitate the results.
Little or no Barlp activity was detected in conditioned media from cells lacking the Ste2p expression plasmid. In cells expressing Ste2p, exposure to agonist resulted in a greater than 8-fold increase in Barlp activity. These data indicate that the Barl plate assay can be used to detect activation of the S. cerevisiae G-protein coupled receptor Ste2p. By analogy, this assay can be used to detect activation of any receptor (including non-homologous e.g. mammalian GPCRs) coupled to the S. cerevisiae pheromone response pathway.
Example 3: Detection of Melatonin 1b Receptor Activation in S. cerevisiae using the Burl Plate Assay This example demonstrates the utility of the Barl plate assay for assessing activation of mammalian G-protein coupled receptors that have been coupled to the S.
cerevisiae pheromone response pathway. For this purpose yeast strains expressing the Melatonin 1 b receptor were constructed.
Plasmid and Strain Construction A plasmid, pcDNA3-hMLlb, containing the complete open reading frame of the human Melatonin 1 b receptor was used as a convenient source of the gene. The sequence of the Melatonin 1 b receptor is known in the art (See e.g., Genbank accession number U25341 ). Primers ' CCTCCGGTCTCCCATGTCAGAGAACGGCTCCTT 3 ' ( SEQ ID NO : 6 ) and 5' CCTCCGGTCTGGGATCCGAGAGCATCTGCCTGGTGC 3' (SEQ ID N0:7) were used to amplify the receptor sequences from this plasmid. The amplified product bears BsaI sites on both the 5' and 3' ends. Digestion with BsaI resulted in a product with an NcoI computable overhang at the 5' end and a BamHI computable overhang at the 3' end. This product was gel purified and subcloned into Cadus 1651 that had been digested with NcoI and BamHI. The resulting plasmid was designated, Cadus 3693.
Cadus 1651 and 3693 were transformed into CY 11645 (described in Example 2) to create CY 11729 and CY 11730, respectively. To verify that Melatonin 1 b receptors expressed in CY 11730 are capable of being activated by agonist and that this activation results in signalling through the pheromone response pathway, the expression of the integrated FUSl-HISS reporter was assessed. Lawns of CY 11729 and CY 11730 cells were prepared on SD LEU-HIS- pH 6.8 plates from SD LEU- pH 6.8 overnight cultures as described in Example 1. After preparation of the lawns, Melatonin (20 pg) was spotted onto the plates and the plates were incubated at 30°C
overnight. Only cells that contained the Melatonin 1 b expression plasmid (CY I 1730) grew and these cells only grew within the zone of diffusion of the applied Melatonin. These data demonstrate the functional expression of the human Melatonin 1 b receptor in yeast and the coupling of this receptor to the pheromone response pathway.
Detection of'~Llelatonin I b Receptor Activation using the 13ar1 Plate Assay Overnight cultures of CY 11729 and CY 11730 were diluted in SD LEU- pH 6.8 medium to an OD600 of 0.2, and allowed to grow for a few hours at 30°C
(to OD600 0.4). The cells were collected by centrifugation, washed 1 X with SD LEU- pH
6.8 medium, and resuspended in 2 ml SD LEU- pH 6.8 medium. Melatonin (10 pg) was added to one aliquot and vehicle (in this case, DMSO) was added to the other.
After 4 hours of incubation at 30°C, the cells were removed either by four successive rounds of centrifugation or by filtration, and 2 p,1 of the conditioned media was applied to a Barl assay plate (described above). A standard curve was also determined with each experiment to quantitate the results. Little or no Barlp activity was detected in conditioned media from cells lacking the melatonin 1 b receptor expression plasmid.
In several experiments addition of I Oug melatonin to cells expressing the receptor resulted in approx. 2-8 fold induction of Barlp. Thus, the Barl plate assay can be used to detect activation of a mammalian G-protein coupled receptor in S.
cerevisiae.
Example 4: Detection of CSa Receptor Activation in S. cerevisiae using the Barl Plate Assay In this example, CSa receptor activation is assessed using the Barl plate assay in a yeast strain expressing the chimeric Ga, GPA 141-Gai3.
Strain Construction The chimeric Ga, GPA141-Gai3, was integrated into the GPAI locus of CY
8034 to create CY 11365. To verify the integration, the expression of the FUSl-reporter in CY 8034 and CY 11365 was compared. Since CY 8034 does not express a G
a protein, the pheromone response pathway is constitutively active in this strain. Thus, integration of GPA141-Gai3 would be expected to decrease expression of the reporter.
As expected, reporter gene expression was reduced in CY 11365, however, it was not completely eliminated. The residual activity is likely due to incomplete coupling of the GPA141-Gai3 chimera to the yeast G(3y.
Cadus 1303, a high copy number yeast expression vector containing the CSa receptor open reading frame fused to the yeast PGK promoter, and Cadus 1289, the vector control, were then transformed into CY 11365 to create CY 11458 and CY
11457, respectively. Expression of the FUSI-HISS reporter in these cells using the Merck CSa receptor agonist, CHA-CHA, was assessed as in Example 2. As expected, only cells expressing the CSa receptor (CY 11458) grew on SD LEU-HIS- pH 6.8 plates containing 1 mM aminotriazole and these cells only grew within the zone of diffusion of the applied CHA-CHA.
Detection of CSa Receptor Activation using the Barl Plate Assay Overnight cultures of CY 11457 and CY 11458 were diluted in SD LEU- pH 6.8 medium to an OD600 of 0.2, and allowed to grow for a few hours at 30°C
(to OD600 0.4). The cells were collected by centrifugation, washed 1 X with SD LEU- pH
6.8 medium, and resuspended in 2 ml SD LEU- pH 6.8 medium. CHA-CHA (10 ICM) was added to one aliquot and vehicle (in this case, DMSO) was added to the other.
After 4 hours of incubation at 30°C, the cells were removed either by four successive rounds of centrifugation or by filtration, and 5 ~.l of the conditioned media was applied to a Barl assay plate (described in Example I ). A standard curve was determined with each experiment to quantitate the results. Exposure of cells expressing CSa receptor to CHA-CHA resulted in increased Baarlp activity, although the induction was less than that seen with Ste2p or Melatonin 1 b receptors.
Example 5: Detection of Barlp-mediated protein degradation This example illustrates an embodiment of the subject assays in which enzyme-mediated cleavage of a-factor by BAR1 p can be used to control the stability of a substrate, which can be used as a selectable event. Cleavage of a-factor by BARlp leaves an N-terminal lysine residue. Proteins with lysine at their N-terminus have been shown to be unstable in yeast (Bachmair and Varshavsky. 1989. Cell. 56:1019).
Therefore, chimeric substrate proteins whose stability in yeast is controlled by the levels of BARlp can be constructed. The a-factor peptide sequence is introduced into the open reading frame of an easily-assayed protein. BARIp induction then causes cleavage of the a-factor sequence within the chimeric substrate and degradation of the substrate by the N-end rule pathway.
The a-factor peptide sequence is fused to the N-terminus of a model substrate, for example, lacZ using standard recmobinant DNA techniques. The construct is placed under the control of a constitutive, moderately expressed promoter in a yeast expression vector. This vector is introduced into yeast cells in which Barlp activity can be induced upon stimulation with an appropriate test compound and LacZ (either enzyme activity or protein levels) is then assayed in cells which have been contacted with test compounds.
Test compounds that induce Barlp are selected based on decreased stability of the chimeric LacZ substrate.
In alternative embodiments, Lac Z can be replaced with, for example, an essential gene (to provide negative selection for Barlp activity) or a repressor protein (to provide positive selection for Barlp activity).
In certain embodiments of the assay, it may be desirable to remove the signals for secretion present at the N- and C-terminus of BARIp to thereby inhibit targeting of Barlp to the secretion machinery. This allows for greater access of Barlp to the chimeric substrate present in the cytoplasm.
Example 6: Construction of PH04/STEIZ Chimerae This example describes the construction of yeast expression plasmids encoding a series of PH04/STEl2 chimerae. These chimerae are used make an easily-assayed gene product, the secreted acid phosphatase PhoSp, pheromone inducible. Changes in gene expression as a consequence of pheromone induction are mediated by the Stel2p transcription factor. In the presence of pheromone signaling Stel2p becomes a potent transcriptional activator of genes whose promoters contain a well-defined DNA
binding site (the pheromone response element, or PRE) (Reviewed by Sprague and Thorner in The Molecular and Cellular Biology of the Yeast Saccharomyces Vol. 2, 1992).
The transcription factor Pho4p is activated when cells are starved for phosphate.
Once activated, Pho4p binds to promoter elements in several genes, including PhoS, and induces their transcription (Reviewed by Johnston and Carlson in The Molecular and Cellular Biology of the Yeast Saccharomyces Vol. 2, 1992). Chimeric transcription factors that contain the transcription activation domains of Ste 12p have been constructed by fusing regions of Stel2p with the DNA binding domain of Pho4p. Expression of these chimerae in yeast results in induction of PhoS expression when the pheromone response pathway is activated. This induction is due to stimulation by the Stel2 transcription activation domain brought into proimity with the PhoS promoter by the Pho4 DNA binding domain. Expression of PhoS can be easily assessed by several well-defined methods for detecting acid phosphatase activity.
A yeast expression plasmid was constructed that contains the yeast ADH
promoter fused to sequences encoding an 11 amino acid nuclear localization signal and the PH04 DNA binding domain (amino acids 227-312). Sequences encoding the PHO4 DNA binding domain were amplified from yeast genomic DNA using the primers 5'CGACTAAGCTTATGGGTGCACCTCCTAAAAAGAAGAGAAAGGTAGCCCCGCACGGATC
GAGCCAT 3' (SEQ ID NO:8) and 5' CCGGAATTCCGTGCTCACGTTC-3'. (SEQ ID N0:9) s The PCR product encodes the Pho4 DNA binding domain flanked by a HindIII
site and sequences encoding a nuclear localization signal on its S' end and an EcoRI
site on its 3' end. This product was digested with HindIII and EcoRI and gel purified.
Plasmid pCD72 (Cadus 3973) was obtained from Dr. J. Broach. It is a high copy number yeast vector containing the ADH promoter and transcription termination sequences as well as i o sequences encoding the GAL=1 DNA binding domain. Digestion of this plasmid with HindIII and EcoRI results in 3 fragments; one containing the vector backbone and the ADH promoter flanked by HindIII overhangs, a second containing the ADH
transcription termination sequences with an EcoRI overhang at its 5' end and a HindIII
overhang at its 3' end, and a third containing the GAL=1 DNA binding domain with a HindIII
overhang at i s its 5' end and an EcoRI overhang at its 3' end. The first two fragments were gel purified and used in a 3-piece ligation with the digested and gei purified PCR
amplification product. The resulting plasmid is designated Cadus 4129.
Fragments of STEI2 were subcloned in frame 3' to the Pho4 DNA binding domain and 5' of the ADH transcription termination sequences by using either the a o EcoRI site, the EcoRI and BamHI sites, or the EcoRI and PstI sites in Cadus 4129. The choice of Stel2 fragments was based on two studies, one in which fusions were made between the Gal4 DNA binding domain and different regions of Stel2 (Song et al Genes & Development, 1991, S(5):741-750) and one in which deletion and insertion mutants of Stel2 were constructed and tested for their ability to restore mating and transcriptional 2 s activity to a stel2d strain (Kirkman-Correia et al Mol Cell Biol, 1993, 13(6):3765-3772).
Plasmids encoding the different Stel2 fragments were obtained from Dr. S.
Fields.
Plasmid Region of Ste I 2p (amino acids) Cadus 4183 l-688 (entire protein) Cadus 4184 214-688 Cadus 4185 214-473 Cadus 4186 1-473 Cadus 4747 insertion of Lys-Leu between as 85 & 86 Cadus 4553 insertion of Ser-Leu between as 103 & 104 Cadus4554 X253-305 Cadus4555 0572-669 Cadus 4556 0588-669 Cadus 4183 was constructed by digesting pOF22[GAL4-STE12 1-688] (Cadus 3918) with EcoRI. The 2.8 kb fragment containing the entire STEI2 open reading frame was gel purified and subcloned into the EcoRI site of Cadus 4129. Cadus 4184 was constructed by digesting pYZl I [GAL4-STE12 214-688] (Cadus 3916) with EcoRI.
The 2.2 kb EcoRI fragment encoding amino acids 214-688 of Stel2p was gel purified and subcloned into the EcoRI site of Cadus 4129. Cadus 4185 was constructed by digesting pXBI [GAL4-STE12 214-473] (Cadus 3972) with EcoRI and BamHI. The 780 by fragment encoding amino acids 214-473 of Ste 12p was gel purified and ligated to Cadus i o 4129 that had been digested with EcoRI and BamHI. Cadus 4186 was constructed by digesting pOG4[GAL4-STE12 1-473] (Cadus 3919) with EcoRI and BamHI. The 1.42 kb fragment encoding amino acids 1-473 of Stel2p was gel purified and ligated to Cadus 4129 that had been digested with EcoRI and BamHI. Primers 5 ' CCGGAATTCATGAAAGTCCAAATAACC 3 ' and (SEQ ID NO:10) 5 ' GCCTGCAGAATTATATTATATCAGGTTG 3 ' (SEQ ID NO:11 ) were used to amplify the insertion and deletion mutants of Stel2p. The amplified products bear EcoRI sites on their 5' ends and PstI sites on their 3' ends.
They were digested with EcoRI and PstI, gel purified, and ligated to Cadus 4129 that had been digested with EcoRI and PstI. Cadus 4747 contains the amplified product of plasmid ao 1k85 (Cadus 3913), Cadus 4553 the product of plasmid Ik103 (Cadus 3910), Cadus 4554 the product of DI I [D253-305] (Cadus 3911, Cadus 4555 the product of D7[D512-699]
(Cadus 3912), and Cadus 4556 the product of D22[D588-669].
Example 7: Detection of Ste2p Activation using the PH09/STEl2 chimerae 2 5 This example demonstrates the use of the PH04/STEl2 chimerae (described in Example 5) to induce expression of the PHOS gene when the pheromone response pathway is activated.
Strain Construction 3o The endogenous PH04 gene was disrupted in CY 1638 (MATa Earl *14-12 tbtl-1 FUSI-HISS trpl ura3 leu2 his3 suc2) with the gene encoding Kanamycin resistance, KanMX2, (Yeast 10:1793-1808). Primers 5' GAGCAAAGGAGACAGAACAAGAGTAGCAGAAAGTCCAGCTGAAGCTTCGTACGC
3 ' and (SEQ ID N0:12) 35 5' CACGTGCTCACGTTCTGCTGTAGGTGACGGATGTAGCATAGGCCACTAGTGGATCTG

3' (SEQ ID N0:13) were used to amplify the KanMX2 gene. The amplification product was flanked by sequences corresponding to the S' and 3' ends of the PHO=t gene. This DNA was transformed into CY 1638. Transforrnants were selected on YEPD + geneticin (200 ~t s g/ml) plates. The disruption of PHO=l in this strain, CY 9788, was verified by assessing acid phosphatase activity in cells grown on phosphate-depleted YEPD medium (100 ml YEPD, 1 ml NH40H, I ml MgS04 [1 M]; let stand 30 min; filter) (Biscon and Thorner, Genetics. 198?). Acid phosphatase activity was assessed using the overlay assay of Toh-a et al (J. Bacteriol, 1973). Cells were patched onto YEPD or phosphate-depleted lo YEPD plates and allowed to grow overnight. For each plate, a mixture of 2 ml of molten I % agarose in 50 mM NaAc pH 4.0, 700 ~tl H20, and 300 p1 a-napthyl acid phosphate (50 mg/ml) was prepared and applied to the plate. Then 1 ml of D-dianisidine fast blue salt B (~Omg/ml in ~0 mM NaAc pH 4.0) was poured onto the plate. The degree of color development is a measure of acid phosphatase activity produced by the i5 patch of cells. As expected CY 9788 had much lower acid phosphatase activity than CY
I 63 8.
The small amount of acid phosphata~e activity observed in CY 9788 is likely that of Pho3p. The PH03 gene also encodes a secreted acid phosphatase, but its expression is not regulated by Pho4p. Instead, its expression is induced under high-phosphate 2o conditions and is further increased by thiamine starvation (Reviewed by Vogel and Hinnene, 1990, Mol. Microbiol., 4(12):2013-2018). Since this gene is not essential and its presence would require that all assays be done under conditions of phosphate starvation, it was disrupted. Primers ' CATGAAGCTTCTCCTACTACCAAGACTG 3 ' and (SEQ ID I~'0:14) 25 5 ' GATCGAATTCGGTAATTTGGAATGGC 3 ' (SEQ ID NO:15) were used to amplify sequences at the 5' end of the PH03 gene. The amplification product which bears a HindIII site at its 5' end and an EcoRI site at its 3' end was digested with HindIII and EcoRI and gel purified. Primers 5 ' GATCGAATTCCTGTTCCACCGGCC' 3 ' and (SEQ ID N0:16) 3 0 5 ' GATCTCTAGAGAGGCGATTGCTGTAATGC 3 ' (SEQ ID N0:17) were used to amplify sequences in the 3' untranslated region of the PH03 gene.
The amplification product which bears an EcoRI site ate its 5' end and an XbaI
site at its 3' end was digested with EcoRI and XbaI and gel purified. The URA3 marked integrating vector pRS406 (Cadus 1011) (Sikorski and Hieter, 1989, Genetics 122:19) was digested 3 5 with HindIII and XbaI, gel purified and used in a three-piece-ligation with the two PCR
products. The resulting two-step disruption plasmid, Cadus 4602, was digested with Hpal and used to transform Cy 9788 to uracil prototrophy.

Subsequent selection for Ura derivitaves of this transformant using S-FOA
yielded CY
11643, bearing the deletion of the Pho3 gene. The disruption of PH03 in CY

was verified by measuring acid phosphatase activity on YEPD plates and on phosphate-depleted YEPD plates as described above. As expected CY 11643 had extremely low s acid phosphatase activity on both plate. Activity of its parent, CY 9788, was very high on the YEPD plate (due to the presence of Pho3p) but very low on the phosphate-depleted SD plate (due to the lack of Pho4p). Finally, activity of the original strain, CY
1638, was very high on both plates indicating that both Pho4 and Pho3 had been disrupted..
io The nine PHO=tISTEl2 chimerae plasmids (described in Example 5) and Cadus 4129, which encodes only the Pho4 DNA binding domain, were then transformed into CY 11643.
Detection of Ste2p Activation by Measuring Pho~p Activity in strains containing the i s PH04/STEI2 Chimerae Cells were grown overnight in SD TRP- media. The overnight cultures were diluted to OD600 0.2 and allowed to grow a few hours (to OD600 0.4). The cultures were split in half (2.5 ml each) and a-factor (25 pg) was added to one aliquot. After 2.5 hours at 30°C, the cells were collected by centrifugation, washed 3 times with H20, once a o with 50 mM NaAc pH 4.0, and resuspended in 250 p1 50 mM NaAc pH 4Ø Acid phosphatase activity was assessed essentially as described by Torriani (Biochim.
Biophys. AClA, 1960, 38:447-460). 100 ~1 cells were added to 400 ~1 p-nitrophenyl phosphate (1 mg/ml in 50 mM NaAc pH 4.0). After 15 min at room temperature, 720 tel saturated NaC03 was added to stop the reaction. The cells were removed by 2 s centrifugation and the optical density at 420 nm was determined.
Activities were normalized to the optical density at 600 nm of 100 ~.1 cells in 900 ~,1 H20.
The results of two independent experiments are summarized in the following Table:
Plasmid - a-factor + a-factor Cadus 4129 +/- +/-Cadus 4183 +/- ++

Cadus 4184 +++ ++++

Cadus 4185 +++ ++++

Cadus 4186 + ++

Cadus 4747 +/- +

Cadus 4553 + +++

Cadus 4554 + ++

-gg_ Cadus 4555 + .~++

Cadus 4556 +/- ++

Cells expressing only the Pho4p DNA binding domain (CY11643 + Cadus 4129) (and no Ste I 2 component) had extremely low acid phosphatase activity that was not increased by exposure to a-factor. In contrast, pheromone-inducible acid phosphatase s activity was observed in al l of the strains expressing Pho4/Ste i 2 chimerae. Two of the chimerae, Pho4/Stel2(214-473) (Cadus 4184) and Pho4/Stel2(1-473) (Cadus 4185), also had high levels of constitutive PhoSp activity, but only a 2-4 fold induction ratio.
Several chimerae had similar induction ratios . Others had very low constitutive activity and similar induction ratios of 5-10 fold. These data demonstrate that Pho4/Stel2 io chimeric transcription factors can be used to render the PHOS gene pheromone-inducible. By extension, this readout can be used to detect activation of any G-protein coupled receptor expressed in S. cerevisiae, as well as activation of any pheromone respoonse pathway component downstream of the receptor. Such activation may be due to modulation by a compound or by protein-protein interaction (e.g., by interaction with 1 s a cloned heterologous gene product).
Example 8: Functional Expression of a Mammalian G Protein-Coupled Receptor and Ligand in an Autocrine Yeast Strain.
In this example, the construction of a yeast cell expressing a G protein-coupled receptor which is suitable for use in the instant assays is described. This example details the following: (1) expression of human CSa receptor in yeast; (2) expression of the native ligand of this receptor, human CSa, in yeast; and (3) activation of the endogenous yeast pheromone pathway upon stimulation of the CSa receptor by CSa when both of these molecules are expressed within the same strain of autocrine yeast.
Following the experimental data the utility of autocrine strains of yeast that functionally express the human CSa receptor is outlined.
Human CSa is a 74 amino acid polypeptide that derives from the fifth component 3 0 of complement during activation of the complement cascade; it is the most potent of the complement-derived anaphylatoxins. CSa is a powerful activator of neutrophils and macrophage functions including production of cytotoxic super oxide radicals and induction of chemotaxis and adhesiveness. In addition CSa stimulates smooth muscle contraction, induces degranulation of mast cells, induces serotonin release from platelets 3 s and increases vascular permeability. The CSa anaphylatoxin can also amplify the inflammatory response by stimulating the production of cytokines. As CSa is a highly potent inflammatory agent, it is a primary target for the development of antagonists to be used for intervention in a variety of inflammatory processes.
The CSa receptor is present on neutrophils, mast cells, macrophages and smooth s muscle cells and couples through G proteins to transmit signals initiated through the binding of CSa.
Expression of the CSa Receptor The plasmid pCDMB-CSaRc, bearing cDNA sequence encoding the human CSa to receptor, was obtained from N. Gerard and C. Gerard (Harvard Medical School, Boston, MA) (Gerard and Gerard 1991 ). Sequence encoding CSa was derived from this plasmid by PCR using VENT polymerase (New England Biolabs Inc., Beverly MA), and the following primers:
15 #1-GGTGGGAGGGTGCTCTCTAGAAGGAAGTGTTCACC (SEQ ID N0:18) #2-GCCCAGGAGACCAGACCATGGACTCCTTCAATTATACCACC (SEQ ID N0:19) Primer #1 contains a single base-pair mismatch (underlined) to CSa receptor cDNA. It introduces an XbaI site (in bold) 201 by downstream from the TAG termination codon z o of the CSa receptor coding sequence. Primer #2 contains two mismatched bases and serves to create an NcoI site (in bold) surrounding the ATG initiator codon (double underlined). The second amino acid is changed from an aspartic acid to an asparagine residue. This is the only change in primary amino acid sequence from the wild type human CSa receptor.
z s The PCR product was restricted with NcoI and XbaI (sites in bold) and cloned into CADUS 1002 (YEp5lNco), a Ga110 promoter expression vector. The sequence of the entire insert was determined by dideoxy sequencing using multiple primers.
The sequence between the NcoI and XbaI sites was found to be identical to the human CSa receptor sequence that was deposited in GenBank (accession #105327) with the 3 o exception of those changes encoded by the PCR primers. The CSa receptor-encoding insert was transferred to CADUS 1289 (pLPXt), a PGK promoter expression vector, using the NcoI and XbaI sites, to generate the CSa receptor yeast expression clone, CADUS 1303.
A version of the CSa receptor which contains a yeast invertase signal sequence 3 s and a myc epitope tag at its amino terminus was expressed in Cadus 1270-transferred yeast under control of a GAL 10 promoter. Plasmids encoding an untagged version of the CSa receptor and a myc-tagged derivative of FUS 1 served as controls. The expression of the tagged receptor in yeast was confirmed by Western blot using the anti-myc monoclonal antibody 9E 10. In the lane containing the extract from the Cadus 1270-transformant, the protein that is reactive with the anti-myc monoclonal antibody 9E 10 was approximately 40 kD in size, as expected. Note that this receptor construct is not identical to the one used in the autocrine activation experiments. That receptor is not tagged, does not contain a signal sequence and is driven by the PGK
promoter.
Expression ojthe Ligand, CSa A synthetic construct of the sequence encoding CSa was obtained from C.
to Gerard (Harvard Medical School, Boston, MA). This synthetic gene had been designed as a FLAG-tagged molecule for the secretion from E coli (Gerard and Gerard (1990) Biochemistry 29:9274-9281 ). The CSa coding region, still containing E coli codon bias, was amplified using VENT polymerase (New England Biolabs Inc., Beverly MA) through 30 cycles using the following primers:
C5a5' = CCCCTTAAGCGTGAGGCAGAAGCTACTCTGCAAAAGAAGATC (SEQ ID NO:2O) C5a3" = GAAGATCTTCAGCGGCCGAGTTGCATGTC (SEQ ID NO:21) A PCR product of 257 by was gel isolated, restricted with AflII and BgIII, and s o cloned into CADUS 1215 (an expression vector designed to express peptide sequences in the context of Mfa) to yield CADUS 1297. The regions of homology to the synthetic CSa gene are underlined. The 5' primer also contains pre-pro a-factor sequence. Upon translation and processing of the pre-pro a-factor sequence, authentic human CSa should be secreted by yeast containing CADUS 1297. The insert sequence in CADUS 1297 a 5 was sequenced in both orientations by the dideoxy method and found to be identical to that predicted by the PCR primers and the published sequence of the synthetic CSa gene (Franke et al. (1988) Methods in Enzymology 162: 653-668).
Two sets of experiments, aside from the autocrine activation of yeast detailed below, demonstrated that CADUS 1297 can be used to express CSa in yeast.
3 0 1 ). CSa was immunologically detected in both culture supernatant and lysed cells using a commercially available enzyme-linked immunosorbent assay (ELISA)(Table 1 ). This assay indicated the concentration of CSa in the culture supernatant to be approximately 50 to 100 nM. In comparison, in data derived from mammalian cells, the binding constant of CSa to its receptor is 1 nM (Boulay et 35 a1.(1991) Biochemistry 30:2993-2999.
2). CSa expressed in yeast was shown to compete for binding with commercially obtained (Amersham Corporation, Arlington Heights, IL), radiolabeled CSa on induced HL60 cells.
Activation of the Pheromone Response Pathway in Autocrine Yeast Expressing the Human CSa Receptor and Human CSa s Activation of the yeast pheromone response pathway through the interaction of C5a with the C5a receptor was demonstrated using a growth read-out. The strain used for this analysis, CY455 (MATa tbtl-1 ura3 ieu2 trill his3 fusl-HIS3 canl stel4::TRP1 ste3* 1156) contains the following significant modifications. A pheromone inducible HIS3 gene , fusl-HIS3, is integrated at the Fusl locus. A hybrid gene containing io sequence encoding the first 41 amino acids of GPA1 (the yeast Ga subunit) fused to sequence encoding human Gai2a (minus codons for the N-terminal 33 amino acids) replaces GPA1 at its normal chromosomal location. The yeast STE14 gene is disrupted to lower the basal level of signaling through the pheromone response pathway.
The yeast a-factor receptor gene, STE3, is deleted. The last two modifications are probably is not essential, but appear to improve the signal-to-noise ratio.
CY455 (MATa tbtl-1 ura3 leu2 trill his3 fusl-HIS3 canl stel4::TRP1 ste3 * 1156) was transformed with the following plasmids:
Callus 1289 + Callus 1215 = Receptor- Ligand-= (R-L-) 2 o Callus 1303 + Callus 1215 = Receptor+ Ligand- = R+L-Cadus 1289 + Callus 1297 = Receptor- Ligand +_ (R-L+) Callus 1303 + Callus 1297 = Receptor+ Ligand +_ (R+L+) Receptor refers to the human C5a receptor.
Ligand refers to human CSa.
Three colonies were picked from each transformation and grown overnight in media lacking leucine and uracil, at pH 6.8 with 25 mM PIPES (LEU URA pH6.8 with 25 mM PIPES). This media was made by adding 0.45 ml of sterile 1 M KOH and 2.5 ml of sterile 1M PIPES pH 6.8 to 100 ml of standard SD LEU- URA- media. After 3 0 overnight growth the pH of this media is usually acidified to approximately pH 5.5.
Overnight cultures were washed once with 25 mM PIPES pH 6.8 and resuspended in an equal volume of media lacking leucine, uracil and histidine (LEU URA HIS pH
6.8 with 25 mM PIPES). The optical density at 600 nm of a 1/20 dilution of these cultures was determined and the cultures were diluted into 25 mM PIPES pH 6.8 to a final OD600 of 0.2. A volume (5u1) of this dilution equivalent to 10,000 cells was spotted onto selective (HIS+ TRp- pH6.8) plates. Only those strains expressing both C5a and its receptor (R+L+) show growth on the selective plates which lack histidine. All test .strains are capable of growth on plates containing histidine. The R+L+ strain will grow on plates containing up to 5 mM aminotriazole, the highest concentration tested.
For verification of pheromone pathway activation and quantification of the stimulation, the activity of the fusl promoter was determined colorometrically using a fusl-lacZ fusion in a similar set of strains. CY878 (MATa tbtl-1 fusl-HIS3 caNl stel4: arpl::LYS2 ste3 * 1156 gpal(41 )-Gai2) was used as the starting strain for these experiments. This strain is a trill derivative of CY455. The transformants for this experiment contained CADUS 1584 (pRS424-fusl-lacZ) in addition to the receptor and ligand plasmids. Four strains were grown overnight in SD LEU URA TRP pH6.8 with to SOmM PIPES to an OD6oo of less than 0.8. Assay of (3-galactosidase activity can be done useing methods known in the art (Guarente 1983). These experiments show that the expression of the CSa receptor and ligand (R+L+) cells results in autocrine stimulation and (3-galactosidase activity.
i5 Projected Uses of the Autocrine CSa Strains:
A primary use of the autocrine CSa strains will be in the discovery of CSa antagonists. Inhibitors of the biological function of CSa would be expected to protect against tissue damage resulting from inflammation in a wide variety of inflammatory disease processes including but not limited to: respiratory distress syndrome (Duchateau ao et al. (1984) Am Rev Respir Dis 130:1058); (Hammerschmidt et al. (1980) Lancet 1:947), septic lung injury (Olson et al. 1985) Ann Surg 202:771 ), arthritis (Banerjee et al. (1989) J. Immuinol 142:2237), ischemic and post-ischemic myocardial injury (Weisman (1990) Science 146:249); (Crawford et al. (1988) Circulation 78:1449) and burn injury (Gelfand et al. (1982) J. Clin Invest 70:1170).
2s The autocrine CSa system as described can be used to isolate CSa antagonists as follows:
1. High throughput screens to identify antagonists of CSa.
A straightforward approach involves screening compounds to identify those 3 o which inhibit growth of the R+L+ strain described above in selective media but which do not inhibit the growth of the same strain or of a R+L- strain in non-selective media.
The counterscreen is necessary to eliminate from consideration those compounds which are generally toxic to yeast. Initial experiments of this type have led to the identification of compounds with potential therapeutic utility.
2. Identification of antagonists using negative selection.
Replacement of the fusl-HIS3 read-out with one of several negative selection schemes (fus 1-URA3/FOA, fusl-GAL 1 /galactose or deoxygalactose, Farl sst2 or other mutations that render yeast supersensitive for growth arrest) would generate a test system in which the presence of an antagonist would result in the growth of the assay strain. Such an approach would be applicable to high-throughput screening of s compounds as well as to the selection of antagonists from random peptide libraries expressed in autocrine yeast. Optimization of screens of this type would involve screening the R+L+ strain at a concentration of aminotriazole which ablates growth of the R+L- strain (for example, 0.6 to 0.8 mM) and counterscreening the R+L-strain at a concentration of aminotriazole which gives an identical growth rate (for example, 0.14 io mM). In addition, the system could employ one of several colorometric, fluorescent or chemiluminescent readouts. Some of the genes which can be fused to the fusl promoter for these alternate read-outs include lacZ (colorometric and fluorescent substrates), glucuronidase 20 (colorometric and fluorescent substrates), phosphatases (e.g.
PH03, PHOS, alkaline phosphatase; colorometric and chemiuminescent substrates), green 1 s protein (endogenous fluorescence), horse radish peroxidase (colorometric), luciferase (chemiluminescence).
The autocrine CSa strains have further utility as follows:
3. In the identification of novel CSa monists from random peptide libraries expressed 2 o in autocrine yeast.
Novel peptide agonists would contribute to structure/function analyses used to guide the rational design of CSa antagonists.
4. In the identification of receptor mutants.
25 Constitutively active, that is, ligand independent, receptors may be selected from highly mutagenized populations by growth on selective media. These constitutively active receptors may have utility in permitting the mapping of the sites of interaction between the receptor and the G-protein. Identification of those sites may be important to the rational design of drugs to block that interaction. In addition, receptors could be 3 o selected for an ability to be stimulated by some agonists but not others or to be resistant to antagonist. These variant receptors would aid in mapping sites of interaction between receptor and agonist or antagonist and would therefore contribute to rational drug design efforts.
3 5 5. In the identification of molecules that interact with Gai2.
Compounds or peptides which directly inhibit GDP exchange from Goci2 would have the same effect as CSa antagonists in these assays. Additional inforniation would distinguish inhibitors of GDP exchange from CSa antagonists. This information could be obtained through assays that determine the following:
1. inhibition by test compounds of Gai2 activation from other receptors, 2. failure of test compounds to compete with radiolabeled CSa for binding to the s CSa receptor, 3. failure of test compounds to inhibit the activation of other Ga subunits by CSa, and 4. inhibition by test compounds of signalling from constitutively active versions of CSa, or other, receptors.
lo Example 9: Construction of Hybrid Ga, Genes Construction of two sets of chimeric yeast/mammalian Ga genes, GPA4~-Ga and GPAlaam-Goc.
The Ga, subunit of heterotrimeric G proteins must interact with both the ~3y complex and the receptor. Since the domains of Ga, required for each of these l s interactions have not been completely defined and since our final goal requires Ga proteins that communicate with a mammalian receptor on one hand and the yeast (3Y
subunits on the other, human-yeast chimeric Ga proteins with an optimized ability to perform both functions were derived. From the studies reported here it was determined that inclusion of only a small portion of the amino terminus of yeast Ga is required to a o couple a mammalian Ga protein to the yeast [3Y subunits. It was anticipated that a further benefit to using these limited chimeras was the preservation of the entire mammalian domain of the Ga protein believed to be involved in receptor contact and interaction. Thus the likelihood that these chimeras would retain their ability to interact functionally with a mammalian receptor expressed in the same yeast cell was expected 2 5 to be quite high.
Plasmid constructions.
pRS416-GPAI (Cadus 1069). An XbaI - SacI fragment encoding the entire 3 o GPAI promotor region, coding region and approximately 250 nucleotides of 3' untranslated region was excised from 10 YCplac 111-GPA 1 (from S. Reed, Scripps Institute) and cloned into YEP vector pRS416 (Sikorski and Hieter, Genetics 122: 19 (1989)) cut with XbaI and SacI.
35 Site-directed mutagenesis of GPAI (Cadus 1075, 1121 and 1122). A 1.9 kb EcoRI fragment containing the entire GPA 1 coding region and 200 nucleotides from the 5' untranslated region was cloned into EcoRI cut, phosphatase-treated PALTER-1 WO 98113513 PCT/LTS97l17159 (Promega) and transformed by electroporation (Biorad Gene Pulser) into DHSaF' bacteria to yield Cadus 1075. Recombinant phagemids were rescued with MI3K07 helper phage and single stranded recombinant DNA was extracted and purified according to the manufacturer's specifications. A new NcoI site was introduced at the s initiator methionine of GPAl by oligonucleotide directed mutagenesis using the synthetic oligonucleotide:
5' GATATATTAAGGTAGGAAACCATGGGGTGTACAGTGAG 3' (SEQ ID N0:22) Positive clones were selected in ampicilIin and several independent clones were sequenced in both directions across the new NcoI site at +1. Two clones containing the correct sequences were retained as Cadus 1121 and 1122.
is Construction of a GPAI-based expression vector (Cadus 1127). The vector used for expression of full length and hybrid mammalian Ga, proteins in yeast, Cadus 1127, was constructed in the following manner. A 350 nucleotide fragment spanning the 3' untranslated region of GPAI was amplified with Taq polymerise (AmpliTaq;
Perkin Elmer) using the oligonucleotide primers A ( 5 2o CGAGGC'TCGAGGGAACGTATAATTAAAGTAGTG 3 ' ) (SEQ ID N0:23) and B ( 5 ' GCGCGGTACCAAGCTTCAATTCGAGATAATACCC 3 ' ) . (SEQ ID N0:24) The 350 nucleotide product was purified by gel electrophoresis using GeneClean II
(Bio 1 O l ) and was cloned directly into the pCRII vector by single nucleotide overlap TA
cloning (InVitrogen). Recombinant clones were characterized by restriction enzyme a s mapping and by dideoxynucleotide sequencing. Recombinant clones contained a novel XhoI site 5' to the authentic GPAI sequence and a novel KpnI site 3' to the authentic GPAI sequence donated respectively by primer A and primer B.
The NotI and SacI sites in the polylinker of Cadus 1 Ol 3 (pRS414) were removed 3 o by restriction with these enzymes followed by filling in with the Klenow fragment of DNA polymerise I and blunt end ligation to yield Cadus 1092. The 1.4 kb PstI -EcoRI
5' fragment of GPAI from YCplacl I i- GPAI containing the GPAI promoter and 5' untranslated region of GPAI was purified by gel electrophoresis using GeneClean (BiolOl) and cloned into PstI - EcoRI restricted Cadus 1013 to yield Cadus 1087. The 35 PCR amplified XhoI - KpnI fragment encoding the 3' untranslated region of GPAI was excised from Cadus 1089 and cloned into XhoI - KpnI restricted Cadus 1087 to yield Cadus 1092. The Notl and Sacl sites in the polylinker of Cadus 1092 were removed by restriction with these enzymes, filling in with the Klenow fragment of DNA
polymerise I, and blunt end ligation to yield Cadus 1110. The region of Cadus 1122 encoding the region of GPAI from the EcoRI site at -200 to +120 was amplified with Vent DNA
polymerise (New England Biolabs, Beverly, MA) with the primers 5' CCCGAATCCACCAATTTCTTTACG 3' (SEQ ID N0:25)and 5' GCGGCGTCGACGCGGCCGCGTAACAGT 3' (SEQ ID N0:26).
The amplified product, bearing an EeoRI site at its 5' end and novel SacI, NotI
and SaII sites at its 3' end was restricted with EcoRI and SaII, gel purified using GeneClean II {Biol01 ), and cloned into EcoRI and SaII restricted Cadus 1110 to yield i o Cadus 1127. The DNA sequence of the vector between the EcoRI site at -200 and the KpnI site at the 3' end of the 3' untranslated region was verified by restriction enzyme mapping and dideoxynucleotide DNA sequence analysis.
PCR amplification of GPA4~-Ga proteins and cloning into Cadus 1127.
cDNA clones encoding the human G alpha subunits Gas, Gai2, Gai3, and S.
cerevisiae I5 GPAI were amplified with Vent thermostable polymerise (New England Bioloabs, Beverly, MA). The primer pairs used in the amplification are as follows:
GaS Primerl . 5'CTGCTGGAGCTCCGCCTGCTGCTGCTGGGTGCTGGAG3' (SacI 5') (SEQ ID N0:27) Primer2: 5'CTGCTGGTCGACGCGGCCGCGGGGGTTCCTTCTTAGAAGCAGC3' 20 (Sill 3') (SEQ ID N0:28) Primer3: 5'GGGCTCGAGCCTTCTTAGAGCAGCTCGTAC3' (XhoI 3') (SEQ
ID N0:29) Gai2 Primer 1 : 5 ' CTGCTGGAGCTCAAGTTGCTGCTGTTGGGTGCTGGGG3 ' (SacIS') 25 (SEQ ID N0:30) Primer2: 5'CTGCTGGTCGACGCGGCCGCGCCCCTCAGAAGAGGCCGCGGT
CC3 ' ( Sal I 3 ' ) (SEQ ID N0:31 ) Primer 3 : 5 ' GGGCTCGAGCCTCAGAAGAGGCCGCAGTC3 ' {XhoI 3') 3 0 (SEQ ID N0:32) Gai3 Primer 1: 5 ' CTGCTGGAGCTCAAGCTGCTGCTACTCGGTGCTGGAG3 ' (SacIS') (SEQ ID N0:33) Primer2:5'CTGCTGGTCGACGCGGCCGCCACTAACATCCATGCTTCTCAAT
35 AAAGTC3 ' (Sill 3') (SEQ ID N0:34) Primer 3 : 5 ' GGGCTCGAGCATGCTTCTCAATAAAGTCCAC3' (XhoI 3') (SEQ
ID N0:35) After amplification, products were purified by gel electrophoresis using GeneClean II
(Bio 1 O 1 ) and were cleaved with the appropriate restriction enzymes for cloning into Cadus 1127.
s The hybrid GPA41-Ga subunits were cloned via a SacI site introduced at the desired position near the 5' end of the amplified genes and a SaII or XhoI
site introduced in the 3' untranslated region. Ligation mixtures were electroporated into competent bacteria and plasmid DNA was prepared from 50 cultures of ampicillin resistant bacteria.
to Construction of Integrating Vectors Encoding GPA4~-Ga Subunits. The coding region of each GPA41-Ga hybrid was cloned into an integrating vector (pRS406 =

AmpR) using the BssHII sites flanking the polylinker cloning sites in this plasmid.
Cadus 1011 (pRS406) was restricted with BssHII, treated with shrimp alkaline i5 phosphatase as per the manufacturer's specifications, and the linearized vector was purified by gel electrophoresis. Inserts from each of the GPA4~-Ga hybrids were excised with BssHII from the parental plasmid, and subcloned into gel purified Cadus 1011.
Construction of GPABAM-Ga Constructs. A novel BamHI site was introduced in frame into the GPA1 coding region by PCR amplification using Cadus 1179 ao (encoding a wildtype GPAl allele with a novel NcoI site at the initiator methionine) as the template, VENT polymerise, and the following primers: Primer A = 5' GCATCCATCAATAATCCAG 3 ~ (SEQ ID N0:36) and Primer B = 5 GAAACAATGGA - TCCACTTCTTAC 3'. (SEQ ID N0:37) The 1.1 kb PCR product was gel purified with GeneClean II (Bio 1 O 1 ), restricted with NcoI and BamHI and as cloned into NcoI-BamHI cut and phosphatased Cadus 1122 to yield Cadus 1605.
The sequence of Cadus 1605 was verified by restriction analysis and dideoxy-sequencing of double-stranded templates. Recombinant GPAa~m-Ga hybrids of Gas, Gai2, and Ga were generated. Construction of Cadus 1855 encoding recombinant GPABam-Ga 16 serves as a master example: construction of the other hybrids followed an analogous 3 o cloning strategy. The parental plasmid Cadus 1617, encoding native Ga 16, was restricted with NcoI and BamHI, treated with shrimp alkaline phosphatase as per the manufacturer's specifications and the linearized vector was purified by gel electrophoresis. Cadus 1605 was restricted with NcoI and BamHI and the 1.1 kb fragment encoding the amino terminal 60% of GPAI with a novel BamHI site at the 3' 3 s end was cloned into the NcoI- and BamHI-restricted Cadus 1617. The resulting plasmid encoding the GPABam-Ga 16 hybrid was verified by restriction analysis and assayed in tester strains ror an ability to couple to yeast Gay and thereby suppress the gpal null phenotype. Two additional GPABam-Ga hybrids, GPABart,-Gas arid GPABam-Gait, described in this application were prepared in an analogous manner using Cadus1606 as the parental plasmid for the construction of the GPAB~m-Ga i2 hybrid and Cadus 1181 as the parental plasmid for the construction of the GPABam-Ga s hybrid.
Coupling by chimeric Ga proteins. The Ga chimeras described above were tested for the ability to couple a mammalian G protein-coupled receptor to the pheromone response pathway in yeast.
io Example 10: Screening for Modulators of G-alpha activity Screens for modulators of Ga activity may also be performed as shown in the following examples for illustration purposes, which are intended to be non-limiting.
Strains CY4874 and CY4877 are isogenic but for the presence of Q205L mutation in the cloned Ga;2 gene cloned into plasmid 1. Strains CY4901 and CY4904 each have a chromosomally integrated chimeric Ga fusion comprising 41 amino acids of gpal at the N terminus of the human Gait gene and are isogenic but for the presence of a constitutively activating mutation in the CSa receptor gene of CY4901. Strain is a gpal mutant which carries only the yeast G~3y subunits and no Ga subunit.
This strain is a control strain to demonstrate specificity of action on the Ga subunit.
I. Suppression of Activation by Mutation of Ga The Q205L mutation is a constitutively activated GTPase deficient mutant of the human Ga;2 gene. Antagonist compounds, chemicals or other substances which act on G
a;2 can be recognized by their action to reduce the level of activation and thus reduce the signal from the fusl-lacZ reporter gene on the second plasmid (Plasmid 2).
A. GTPase Ga;2 Mutants test component = gpa4~-Ga;2 {Q2osL) control component = gpa4~-Ga;z As well as the CY4874 and CY4877 constructs detailed above, similar strains with fusl-His3 or fus2-CAN-1 growth readouts may also be used. The fusl-His3 strains are preferred for screening for agonists and the fus2-CAN 1 strains are preferred for antagonist screens.
Readout test effect of Ga;z antagonist control strain strain fusl-HIS3 CY4868 inhibit growth of-HIS CY4871 +AT (Aminotriazole) fusl-lacZ CY4874 reduce (3-gal activity CY4877 fus2-CAN1 CY4892 induce growth on CY4386 canavanine In each case an antagonist should cause the test strain to behave more like the control strain.
B. GTPase Gas Mutants (Ga Specificity) test component = Gas(Qzz~L) control component = Gas Readout test effect of Ga;z anta; onist control strain strain fusl-HIS3 CY4880 none CY4883 fusl-lacZ CY4886 none CY4889 fus2-CAN 1 CY4895 none CY4898 In each case a non-specific antagonist would cause the test strain to behave more like the control strain.

to Additional media requirements: -TRP for Ga plasmid maintenance in fusl-HIS3 and fus2-CAN1 screens and -TRP -URA for Ga and fusl-lacZ plasmid maintenance in fusl-lacZ screen.
II. Suppression of Activatlon by Receptors Constitutively Activated CSa Receptors test component = CSaR* (Pi84L, activated CSa Receptor) a o control component = CSaR
The CSaR* mutation has a Leucine residue in place of the Proline residue of the wild-type at position 184 of the amino acid sequence.

Readout test effect of Ga.;2 antagonist control strain strain fusl-HIS3 CY4029 inhibit growth of-HIS CY2246 +AT (Aminotriazole) fusl-lacZ CY4901 reduce (3-gal activity CY4904 fus2-CAN 1 CY4365 induce growth on CY4362 canavanme In each case an antagonist should cause the test strain to behave more like the control strain.
s Additional media requirements: -LEU for receptor plasmid maintenance in full-and fus2-CAN 1 screens and -LEU-URA for receptor and fus 1-laeZ plasmid maintenance in fusl-lacZ screen, non-buffered yeast media (pH 5.5).
io Example 1l: Identification of a surrogate ligand using expression of a random peptide library in yeast expressing an orphan mammalian receptor FPRL-I (formyl peptide receptor-like 1 ) is a structural homolog of the formyl peptide receptor (FPR). FPR is a G protein-coupled receptor, expressed on neutrophils i5 and phagocytic cells, that is stimulated by N-formyl peptides of bacterial origin.
Specific binding of the natural ligand, f Met-Leu-Phe, stimulates transduction of a signal to mobilize calcium, resulting in cellular changes including chemotaxis and the release of granule contents. Low stringency hybridization of HL60 cDNA
libraries with an FPR cDNA probe permitted the identification of the related receptor, FPRL-1 ao (Murphy et al. supra; Ye et al. supra). The FPRL-1 cDNA encodes a 351 amino acid protein with 69% sequence homology to FPR (Murphy et al. supra) FPR and FPRL-I
were found to co-localize to human chromosome 19 and to have a tissue expression pattern identical to that of FPR, i.e., expression is restricted to cells of myeloid origin (Murphy et al. supra). Ye et al. (supra) demonstrated weak binding of f Met-Leu-Phe 25 (uM concentrations) to fibroblasts transfected with FPRL-I cDNA. In contrast, Murphy et al. (supra) could not detect binding of N-formyl peptides to Xenopus oocytes transfected with FPRL-1 cDNA. FPRL-1 appears to be an orphan receptor whose specific ligand differs from the formyl peptide ligands to which FPR responds.
In this example experiments detailing the following will be described: (1) WO 98/13513 PCT/US97t17159 establishment of a strain of yeast designed to express the human orphan G
protein-coupled receptor FPRL-1; (2) expression of a random peptide library in the aforementioned strain of yeast; and (3) activation of the endogenous yeast pheromone pathway upon stimulation of the FPRL-1 receptor by a peptide encoded by a random library expressed within the same strain of yeast.
Preparation of FPRL-1 Yeast Expression Vector A plasmid, pFPRLI-L31, containing a 2.6 kb EcoRI-Xhol fragment encoding the FPRL-1 cDNA in the BluescriptIISK+ vector was obtained from Philip Murphy (NIH).
i o The sequence encoding FPRL 1 was amplified by the polymerase chain reaction using VENT polymerase (New England Biolabs, Inc., Beverly, MA) through 20 cycles and the following oligonucleotide primers:
#I 5' GGCGCCCGGTCTCCCATGGAAACCAACTTCTCCACT (SEQ ID NO:38) #2 5' GGCGCCCGGTCTCCGATCCCATTGCCTGTAACTCAGTCTC (SEQ ID N0:39) The PCR product was purified, restricted with BsaI and cloned into Cadus 1651 (pIPBX-I ), a PGK promoter-driven expression vector, using NcoI and BamHI
sites, to yield CADUS 2311. The sequence of the entire insert was determined and found to be a o identical to the FPRL-I sequence deposited in GenBank (accession number M84562).
Preparation of Random Oligonucleotides Library-Recycling Protocol to Identify a Surrogate Ligand The yeast strain CY 1141 (MATalpha far 1 * I 441 tbt I - I fus 1-HI S3 can 1 a 5 ste l4:arpl:;LYS2 ste3* 1156 gpal(41 )-Galphai2 lys2 ura3 leu2 trp 1 his3) was used in the experiments that follow. CYI 141 contains a pheromone inducible HIS3 gene, fusl-HIS3 integrated at the FUS1 locus and a hybrid gene encoding the first 41 amino acids of GPA 1 (yeast G alpha) fused to sequence encoding human G alphai2 (lacking codons encoding the N-terminal 33 amino acids) replacing GPA1 at its chromosomal locus.
3o The yeast STE14 gene is disrupted to lower the basal level of signaling through the pheromone response pathway. The yeast a-factor receptor gene, STE3, is deleted.
CY1141 was transformed with Cadus 2311 to yield CY6571, a strain expressing the human orphan receptor, FPRL-1.
CY6571 exhibited LIRMA (ligand independent receptor mediated activation), 3 5 that is, activation of the yeast pheromone pathway in the absence of ligand. It was determined that the yeast growth on selective media that resulted from LIRMA
was eliminated by the additional of 2.Smillimolar concentrations of 3-aminotriazole (AT).

AT is an inhibitor of the HISS gene product that serves to reduce background growth.
Therefore, selection protocols aimed at the identification of surrogate ligands for the FPRL-1 receptor were carried out at this concentration of AT.
CY6571 was inoculated to 10 mls of standard synthetic media (SD) lacking s leucine (-Leu) and incubated overnight at 30°C. The 10 ml overnight culture was used to inoculate 50 mls of YEPD; this culture was incubated at 30°C for 4.5-5 hours at which time the cells were harvested and prepared for transformation with DNA
encoding a random peptide library [alpha-NNK (6.24.94)] encoding tridecapeptides of random sequence, by electroporation. Post electroporation (in 0.2 em cuvettes, 0.25 ~F, i o 20052, 1.5 kV) the cells were immediately diluted in 1 ml ice-cold 1 M
sorbitol and 1 OOp L aliquots were placed onto 10 synthetic media plates (pH6.8) lacking leucine and uracil (-Leu-Ura). The plates were incubated at 30°C for 2-4 days at which time two replicas of each original transformation plate were made to synthetic media (pH6.8) lacking leucine, uracil and histidine and supplemented with 2.SmM AT(-Leu-Ura-His+2.SmM
i5 AT). The replicas were incubated at 30°C for 3-5 days. Post incubation the colonies present on the replica sets of two were scraped from the plates into a total of 10 mls of H20 (5 mls each plate). The OD600 of each cell suspension was determined and crude plasmid isolations were done on 8-16 OD units of cells for each pool. A total of eight pools resulted, due to lower numbers of yeast colonies present in four sets of plates. The a o pellets obtained from these crude plasmid isolations (the so called "smash and grab"
technique, Methods in Yeast Genetics - A Laboratory Manual, 1990, M.D. Rose, F.
Winston and P. Heifer. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y.), were resuspended in 40~L of 10 mM Tris, I mM EDTA, pH8.0 and 1~L was used to transform E. coli by electroporation (0.1 cm cuvettes, 0.25 ~F, 20052, 1.8 kV).
25 Post electroporation the cells were immediately diluted into 1 ml 2XYT
media and incubated, with shaking, at 37°C for 30 minutes after which time the cells were used to inoculate 50 mls of 2xYT supplemented with 100 ug/ml ampicillin. The 10 resulting cultures were incubated at 37°C overnight. Plasmid DNA was isolated from each of these bacteria cultures using Qiagen columns (Qiagen, Inc., Chatsworth, CA)).
Each 3 o plasmid DNA pellet was resuspended in SO~L Tris 1 OmM, EDTA 1 mM, pH 8Ø
Strain CY6571 was transformed with 1 pL of each plasmid pool by electroporation. Post electroporation the cells were diluted into 400~L 1M
sorbitol.
From each electroporated cell suspension, 1 pL and 400~L of cells were plated on -Leu-Ura synthetic media, pH6.8 to yield "low density" and "high density" platings.
The 35 plates were incubated at 30°C for 3 days, at which time replicas of both the low and high density plates were made to -Leu-Ura-His+2.SmM AT. For those cases where enrichment for a plasmid capable of conferring a His+ phenotype had occurred, this would be reflected by an amplified number of His+ colonies on both the low and high density plates visible at days 2-3, although the amplification would be most obvious on the plates that had received a high density of cells. In the FPRL-I experiment 1/8 pools showed amplification of His+ colonies. The cells were scraped from this plate into 5 mls of H20, the OD600 of the cell suspension was determined and a crude plasmid isolation was done on 15 OD units of yeast cells. The pellet obtained was resuspended in 40pL l OmM Tris, 1 mM EDTA, pH8.0 and 1 pL was used to transform E coli.
Plasmid DNA was isolated by miniprep from 3 ml 2XYT cultures of single bacterial colonies resulting from this transformation. 10 DNA pellets (A 1 through A I
0) deriving i o from individual bacterial colonies were resuspended in 20p.L 10 mM Tris I
mM EDTA, pH8.0 and used to transform CY6571 (containing the FPRL-1 expression vector) and CY6263 (CYl 141 containing a control expression vector lacking any receptor sequence) by electroporation. Cadus 1625, a control vector lacking sequences encoding a peptide, was included and used to transform both the receptor+ and receptor- strains of yeast.
i5 Transformants were first selected on -Leu-Ura, pH6.8 then three yeast transformants of each type (from 11 CY657i transformations and 11 CY6263 transformations) were patched to -Leu-Ura, pH6.8 to expand the colonies. Once expanded, streaks of the transformants were made on -Leu-Ura-His+2.SmM AT to test for growth in the absence of histidine. All plasmids except the one denoted A2 conferred a growth advantage on 2 o media lacking histidine to yeast bearing the FPRL-1-encoding plasmid but not to yeast lacking the receptor plasmid. The peptide sequence found to be encoded by plasmids A1 and A3-A10 is: SerLeuLeuTrpLeuThrCysArgProTrpGluAlaMet, (SEQ ID N0:40) and is encoded by the nucleotide sequence 5 ' -TCT CTG CTT TGG CTG ACT TGT
CGG CCT TGG GAG GCG ATG-3'. (SEQ ID N0:41) Activation of the Pheromone Response Pathw~ in Yeast Expressing the FPRL I
Receptor and Peptide A~onist For verificatiin of pheromone pathway activation and quantification of the stimulation, the activity of the fusl promoter was determined colorimetrically using a 3 o fus 1-lacZ fusion in a parallel set of test strains. CY 1141, described above, was used as the recipient strain for these experiments. Transformants contained CADUS 1584 (pRS424-fusl-IacZ) in addition to receptor (R+~-) and Iigand (L+~-) plasmids.
Four strains (bearing the identical plasmids) were grown overnight in minimal media lacking leucine, uracil, and tryptophan, pH8.6. The overnight cultures were used to inoculate -3 5 Leu -Ura -Trp pH6.8 media and these new cultures were grown for approximately 4.5-S
hours to an OD6oo of less than 0.4. Assay of (3-galactosidase activity (Guarente 1983) in cells from these cultures yielded the following results:

CY1141/CADUS 2311/peptide Al/CADLJS 1584 R+L+ 28 units CY 114 i /CADUS 2311 /CADUS 1625/CADUS 1584 R~L- 3 units CY1141/CADUS 1289/peptide A1/CADUS 1584 R-L+ 3.5 units CY1141/CADUS 1289/CADUS 1625/CADUS 1584 R-L- 3.9 units s The presence of receptor and peptide-encoding plasmids resulted in an average 8-fold stimulation over background levels of ~3-galactosidase.
Example 12: Identification of surrogate ligands using expression of a random peptide library in yeast expressing the orphan mammalian receptor, MDR-15.
io In a similar manner a plasmid encoding the monocyte derived receptor monocyte-derived receptor 15 (MDR15; Barella et al. (1995) Biochem. J. 309:773-9) was used to construct a yeast strain (CY6573) expressing this receptor. This receptor is an alternative spliced form of the Burkitt's lymphoma receptor 1 (BLRI) encoded by a human Burkitt's lymphoma cDNA {Dobner et al. (1992) Eur. J. Immunol. 22, 2795-15 2799). Strain CY6573 was transformed in a similar manner with the NNK13 library, and, following selection on ten -Leu-Ura (4.4 x 105 colonies per plate), replica plated to -Leu-Ura-His+ 1 mM AT plates. Upon reisolation of plasmid pools and re-transformation into strain CY6573; eight of ten pools showed signicantly enriched colony formation on -Leu-Ura-His+ 1 mM AT plates. Eight unique plasmids derived 2o from these pools when retransformed into CY6573 conferred growth on -Leu-Ura-His+
1 mM AT plates. One of these plasmids failed to confer growth in a yeast strain lacking the MDR15 receptor.
Example 13: Identification of a ligand using expression of a random peptide library as in yeast expressing the human thrombin receptor The receptor for thrombin, a G protein-coupled receptor, is present on numerous cell types including platelets, vascular smooth muscle, fibroblasts and on a subset of cells that function in immunity. Thrombin, a serine protease, binds to and cleaves the receptor molecule at residue 41, generating a new receptor N-terminus. The post-3 o cleavage N-terminal residues then act as a "tethered ligand' to activate the receptor molecule (Vu et al. 1994). In platelets, signaling through the thrombin receptor has been shown to result in numerous effects including stimulation of phospholipase C, mobilization of intracellular Ca2+ and inhibition of adenylyl cyclase.
In this example experiments that detail the following will be described (1) 3 s establishment of a strain of yeast designed to express the human G protein-coupled receptor for thrombin; (2) expression of a random peptide library in the afore-mentioned strain of yeast and (3) activation of the endogenous yeast pheromone pathway upon stimulation of the thrombin receptor by peptides encoded by a random library expressed within the same strain of yeast.
Preparation of a Yeast Expression Vector for a Mammalian Thrombin Receptor The human thrombin receptor was amplified by PCR from pcDNA3:Hu-Thr9b-5' (Bristol Myers Squibb) using the following oligonucleotides:
5 ' GGGCCATGGGGCCGCGGCGGTTG 3 ' (SEQ ID N0:42) 5 ' CCCGGATCCTAAGTTAACAGCTTTTTGTATAT 3 ' (SEQ ID N0:43) i o The amplified product was purified by gel electrophoresis, restricted with NcoI and BamHI and ligated to NcoI and BamHI-cut CADUS 1871, a PGK promoter-driven expression vector, to yield CADUS 2260. Cloning into CADUS 1871 introduces a novel stop codon preceded by the triplet GlySerVal after the authentic carboxy terminal codon of the human thrombin receptor (threonine). In addition, an invertase signal i5 sequence is fused to the authentic amino terminus of the receptor.
CY7467 exhibited LIRMA {ligand independent receptor mediated activation), that is, activation of the yeast pheromone pathway in the absence of ligand.
It was determined that the yeast growth on selective media that resulted from LIRMA
was eliminated by the addition of 2.5 miilimolar concentrations of 3-aminotriazole (AT). AT
a o is an inhibitor of the HIS3 gene product that serves to reduce background growth.
Therefore, selection protocols aimed at the identification of novel peptide ligands for the human thrombin receptor were carried out at this concentration of AT.
Preparation of Random Oligonucleotide Library z s As described above.
RecyclinQ Protocol to Identify a Surrogate Ligand The yeast strain CYl 141 {MATalpha furl * 1442 tbtl-1 fusl-HIS3 cant ste 14: arp 1::LYS2 ste3 * 1156 gpal (41 )-Galphai2 lys2 ura3 leu2 trp l his3) was ao transformed with CADUS 2260 to yield strain CY7467, expressing the human thrombin receptor. CY7467 was inoculated to 10 mls of standard synthetic media (SD) lacking leucine (-Leu) and incubated overnight at 30 C. The 10 ml overnight culture was used to inoculate 50 mls of YEPD media; this culture was incubated at 30 C for 4.5-5 hours at which time the cells were harvested and prepared for transformation with DNA
encoding a random peptide library [alpha-NNK (6.24.94)] by electroporation. Post electroporation (in 0.2 cm cuvettes, 0.25 mF, 200W, 1.5 kV) the cells were immediately diluted in 1 ml ice-cold 1 M sorbitol and 1 OOmL aliquots were plated onto 10 synthetic media plates (pH6.8) lacking leucine and uracil (-Leu-Ura). The plates were incubated s at 30 C for 2-4 days at which time two replicas of each original transformation plate were made to synthetic media (pH6.8) lacking leucine, uracil and histidine and supplemented with 2.5mM AT(-Leu-Ura-His+ 2.5mM AT). The replicas were incubated at 30 C for 3-5 days. Post incubation the colonies present on the replica sets of two were scraped from the plates into a total of 10 mls of H20 (5 mls each plate).
1 o The OD600 of each cell suspension was determined and crude pIasmid isolations were done on 8-16 OD units of cells for each pool. A total of ten pools resulted.
The pellets obtained from these crude plasmid isolations were resuspended in 40mL of 10 mM
Tris, 1 mM EDTA, pH8.0 and 1 mL was used to transform E. coli by electroporation {0.1 cm cuvettes, 0.25 mF, 200W, 1.8 kV). Post electroporation the cells were immediately z5 diluted into 1 ml 2XYT media and incubated, with shaking, at 37 C for 30 minutes after which time the cells were used to inoculate 50 mls of 2xYT supplemented with ug/ml ampicillin. The 10 resulting cultures were incubated at 37 C overnight.
Plasmid DNA was isolated from each of these bacterial cultures using Qiagen columns (Qiagen, Inc., Chatsworth, CA). Each plasmid DNA pellet was resuspended in 50mL Tris l OmM, z o EDTA 1 mM, pH 8Ø
Strain CY7467 was transformed with 1 mL of each plasmid pool by electroporation. Post electroporation the cells were diluted into 400mL 1M
sorbitol.
From each electroporated cell suspension, 1 mL and 400mL of cells were plated on -Leu-Ura synthetic media, pH6.8 to yield "low density" and "high density" platings.
The 2 5 plates were incubated at 30 C for 3 days, at which time replicas of both the low and high density plates were made to -Leu-Ura-His+ 2.5mM AT. For those cases where enrichment for a plasmid capable of conferring a His+ phenotype had occurred, this would be reflected by an amplified number of His+ colonies on both the low and high density plates visible at days 2-3, although the amplification would be most obvious on 3 o the plates that had received a high density of cells. In this experiment 3/10 pools showed amplification of His+ colonies. The cells from each of these plates were scraped into 5 mls of H20, the OD600 of the cell suspensions were determined and crude plasmid isolations were done on 8-16 OD units of yeast cells. The pellets obtained were resuspended in 40mL 10 mM Tris, 1 mM EDTA, pH8.0 and 1mL was 3 s used to transform E. coli. Plasmid DNA was isolated by miniprep from 3 ml cultures of single bacterial colonies resulting from these transformations (three bacterial colonies for each DNA pool were processed in this way). DNAs deriving from three individual bacterial colonies per pool were resuspended in 20mL 10 mM Tris 1 mM
EDTA, pH8Ø The three DNAs derived per pool were sequenced and found to encode identical peptides. Thus three differing DNA sequences were derived, one representing each amplified pool. One plasmid representing each of the three original amplified s pools was used to transform CY7467 (containing the thrombin receptor expression vector) and CY6263 (CY1141 containing a control expression vector lacking any receptor sequence) by electroporation. CADUS 1625, a control vector lacking sequences encoding a peptide was included and used to transform both the receptor+ and receptor- strains of yeast. CADUS 1651, a control vector lacking sequences encoding a i o receptor included and used to transform both the ligand+ and ligand-strains of yeast..
Transformants were first selected on -Leu-Ura, pH6.8, then two yeast transformants of each type were patched to -Leu-Ura, pH6.8 to expand the colonies. Once expanded, streaks of the transformants were made on -Leu-Ura-His+ 2.SmM AT to test for growth in the absence of histidine. One of the three plasmids tested conferred a growth 1 s advantage on media lacking histidine to yeast bearing the thrombin-encoding plasmid but not to yeast lacking the receptor plasmid. The peptide sequence encoded by this plasmid is: Val-Cys-Pro-Ala-Arg-Tyr-Val-Leu-Pro-Gly-Pro-Val-Leu (SEQ ID
N0:45)and was encoded by the nucleotide sequence GTT TGT CCT GCG CGT TAT
GTG CTG CCT GGG CCT GTT TTG . (SEQ ID N0:44) r -1~g-SEQUENCE LISTING
(1) GENERAL INFORMATION:
(i) APPLICANTS: CADUS PHARMACEUTICAL CORPORATION
(ii) TITLE OF INVENTION: METHODS AND COMPOSITIONS FOR
IDENTIFYING RECEPTOR EFFECTORS
(iii) NUMBER OF SEQUENCES: 47 (iv) CORRESPONDENCE ADDRESS:
(A) ADDRESSEE: BORDEN ELLIOT SCOTT & AYLEN
(B) STREET: 1000-60 QUEEN STREET
(C) CITY: OTTAWA
(D) PROVINCE: ONTARIO
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(F) POSTAL CODE: K1P 5Y7 (v) COMPUTER READABLE FORM:
(A) MEDIUM TYPE: Floppy disk (B) COMPUTER: IBM PC compatible (C) OPERATING SYSTEM: PC-DOS/MS-DOS
(D) SOFTWARE: PatentIn Release #1.0, Version #1.25 (vi) CURRENT APPLICATION DATA:
(A) APPLICATION NUMBER: 2,266,543 (B) FILING DATE: 24-SEP-1997 (vii) PRIOR APPLICATION DATA:
(A) APPLICATION NUMBER: US 08/718,910 (B) FILING DATE: 24-SEP-1996 (vii) PRIOR APPLICATION DATA:
(A) APPLICATION NUMBER: US 08/851,469 (B) FILING DATE: 05-MAY-1997 (viii) ATTORNEY/AGENT INFORMATION:
(A) NAME: JOACHIM T. FRITZ
(B) REGISTRATION NUMBER: 4173 (C) REFERENCE/DOCKET NUMBER: PAT 44188W-1 (ix) TELECOMMUNICATION INFORMATION:
(A) TELEPHONE: (613) 237-5160 (B) TELEFAX: (613) 787-3558 (2) INFORMATION FOR SEQ ID NO:1:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 25 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: cDNA
(xi) SEQUENCE DESCRIPTION: SEQ ID NO:1:

(2) INFORMATION FOR SEQ ID N0:2:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 25 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: cDNA
(xi) SEQUENCE DESCRIPTION: SEQ ID N0:2:

(2) INFORMATION FOR SEQ ID N0:3:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 26 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: cDNA
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(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 11 amino acids (B) TYPE: amino acid (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (v) FRAGMENT TYPE: internal (x) FEATURE:
(A) NAME/KEY: Modified site (B) LOCATION: 1 (D) OTHER INFORMATION: /note= Trp is DABYL(GABA)modified (ix) FEATURE:
(A) NAME/KEY: Modified site (B) LOCATION: 11 (D) OTHER INFORMATION: /note= Tyr is EDANS modified (xi) SEQUENCE DESCRIPTION: SEQ ID N0:4:
Trp Leu Gln Leu Lys Pro Gly Gln Pro Met Tyr (2) INFORMATION FOR SEQ ID N0:5:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 11 amino acids (B) TYPE: amino acid (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (v) FRAGMENT TYPE: internal (x) FEATURE:
(A) NAME/KEY: Modified site (B) LOCATION: 1 (D) OTHER INFORMATION: /note= Trp is CBZ modified (ix) FEATURE:
(A) NAME/KEY: Modified site (B) LOCATION: 11 (D) OTHER INFORMATION: /note= Tyr is Rhodamine modified (xi) SEQUENCE DESCRIPTION: SEQ ID N0:5:
Trp Leu Gln Leu Lys Pro Gly Gln Pro Met Tyr (2) INFORMATION FOR SEQ ID N0:6:
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(A) LENGTH: 65 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: cDNA
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CATGAAGCTT CTCCTACTAC CAAGACTG 2g (2) INFORMATION FOR SEQ ID N0:15:
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GATATATTAA GGTAGGAAAC CATGGGGTGT ACAGTGAG 3g (2) INFORMATION FOR SEQ ID N0:23:
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Ser Leu Leu Trp Leu Thr Cys Arg Pro Trp Glu Ala Met (2) INFORMATION FOR SEQ ID N0:41:
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(2) INFORMATION FOR SEQ ID N0:42:

(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 23 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: other nucleic acid (xi) SEQUENCE DESCRIPTION: SEQ ID N0:42:

(2) INFORMATION FOR SEQ ID N0:43:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 32 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: other nucleic acid (xi) SEQUENCE DESCRIPTION: SEQ ID N0:43:

(2) INFORMATION FOR SEQ ID N0:44:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 39 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: other nucleic acid ( i.x) FEATURE
(A) NAME/KEY: CDS
(B) LOCATION: 1..39 (xi) SEQUENCE DESCRIPTION: SEQ ID N0:44:

Val Cys-Pro Ala Arg Tyr Val Leu Pro Gly Pro val Leu (2) INFORMATION FOR SEQ ID N0:45:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 13 amino acids (B) TYPE: amino acid (D) TOPOLOGY: linear (ii) MOLECULE TYPE: protein (xi) SEQUENCE DESCRIPTION: SEQ ID N0:45:
Val Cys Pro Ala Arg Tyr Val Leu Pro Gly Pro Val Leu (2) INFORMATION FOR SEQ ID N0:46:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 10 amino acids (B) TYPE: amino acid (D) TOPOLOGY: linear (ii) MOLECULE TYPE: protein (xi.) SEQUENCE DESCRIPTION: SEQ ID N0:46:
Leu Leu Leu Leu Gly Ala Gly Glu Ser Gly (2) INFORMATION FOR SEQ ID N0:47:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 9 amino acids (B) TYPE: amino acid (D) TOPOLOGY: linear (ii) MOLECULE TYPE: protein (xi) SEQUENCE DESCRIPTION: SEQ ID N0:47:
Leu Glu Lys Gln Arg Asp Lys Asn Glu

Claims (36)

CLAIMS:
1. An assay for identifying a compound that modulates a heterologous receptor expressed by a yeast cell comprising:
i) providing a yeast cell which expresses a heterologous receptor which is functionally integrated into an endogenous yeast signaling pathway, wherein said yeast cell comprises an endogenous gene operatively linked to a heterologous promoter at the natural location of said endogenous gene in said yeast cell, said promoter being responsive to signals produced by said yeast signaling pathway;
ii) contacting the yeast cell with a test compound; and iii) detecting an alteration in a signal produced by the endogenous yeast gene;
to thereby identify a compound that modulates the heterologous receptor.
2. The assay of claim 1, wherein said signaling pathway is a yeast pheromone response pathway.
3. The assay of claim l, wherein said step of detecting comprises measuring transcription of said gene.
4. The assay of claim 1, wherein said step of detecting comprises measuring the amount or activity of an endogenous yeast protein encoded by said gene.
5. The assay of claim 1, wherein said test compound is derived from a library of non-peptidic compounds.
6. The assay of claim 1, wherein the detecting step comprises detecting a change in the activity of an endogenous enzyme expressed by said yeast cell in response to a signal produced by the endogenous yeast signaling pathway.
7. The assay of claim 6, wherein said signaling pathway is a yeast pheromone response pathway.
8. The assay of claim 6, wherein the step of detecting comprises measuring the enzymatic activity of the enzyme.
9. The assay of claim 6, wherein said step of detecting comprises measuring the effect of the enzyme on the growth of a test yeast strain which does not express a functional BAR1 enzyme.
10. The assay of claim 6, wherein said enzyme is BAR1 protease.
11. The assay of claim 10, wherein said step of detecting comprises determining the cleavage of a substrate having a BAR1 peptide recognition sequence.
12. The assay of claim 11, wherein said substrate is naturally occurring.
13. The assay of claim 11, wherein said BAR1 substrate comprises at least one detectable label.
14. The assay of claim 11, wherein said substrate is a chimeric substrate comprising:
a first polypeptide which, upon cleavage by BAR1, exposes an amino terminal Lys; and a second polypeptide linked to the carboxy terminus of said first polypeptide;
wherein said step of detecting comprises measuring the stability of the chimeric substrate.
15. The assay of claim 11, wherein said substrate is not naturally occuring.
16. The assay of claim 15, wherein said substrate comprises the compound of SEQ
ID NO:4.
17. The assay of claim 15, wherein said substrate comprises the compound of SEQ
ID NO:5.
t 8. An assay for identifying a compound that modulates a heterologous receptor expressed by a yeast cell comprising:
1) providing a yeast cell which expresses a heterologous receptor which is functionally integrated into an endogenous yeast signaling pathway, wherein said yeast cell comprises a gene which encodes a detectable protein and a chimeric nucleic acid construct, said construct comprising:
a first segment derived from a first gene, said first segment encoding a polypeptide that is activated by a yeast signaling pathway, and a second segment derived from a second gene, said second segment encoding of a polypeptide that binds a DNA sequence in the regulatory region of said gene which encodes a detectable protein;
such that said gene is rendered responsive to activation of a yeast signaling pathway;
ii) contacting the yeast cell with a test compound; and iii) detecting an alteration in a signal produced by said detectable protein to thereby identify a compound that modulates the heterologous receptor.
19. The assay of claim 18, wherein said step of detecting an alteration in a signal produced by said detectable protein comprises measuring transcription of said gene encoding said detectable protein.
20. The assay of claim 18, wherein said signaling pathway is a yeast pheromone response pathway.
21. The assay of claim 20, wherein said first segment is derived from a Ste 12 gene.
22. The assay of claim 21, wherein said first segment encodes a polypeptide comprising amino acids 1-688 of Ste12.
23. The assay of claim 20, wherein said second segment is derived from a Pho4 gene.
24. The assay of claim 23, wherein said second segment encodes a polypeptide comprising amino acids 227-312 of Pho4.
25. The assay of claim 23, wherein said yeast cell comprises a mutation in its endogenous Pho4 gene.
26. The assay of claim 20, wherein said gene which encodes a detectable protein is the endogenous yeast Pho5 gene.
27. .The assay of claim 26, wherein said step of measuring comprises detecting the activity of PHO5 acid phosphatase.
28. An assay for identifying a compound that modulates a heterologous orphan G
protein-coupled receptor expressed by a yeast cell comprising:
i) providing a yeast cell which expresses a heterologous orphan G protein-coupled receptor which is functionally integrated into an endogenous yeast signaling pathway, wherein said yeast cell comprises an endogenous gene operatively linked to a heterologous promoter at the natural location of said endogenous gene in said yeast cell, said promoter being responsive to signals produced by said yeast signaling pathway;
ii) contacting the yeast cell with a non-peptidic test compound; and iii) detecting an alteration in a signal produced by the endogenous yeast gene;
to thereby identify a non-peptidic compound that modulates the heterologous orphan G-protein coupled receptor.
29. The assay of claim 28, wherein said non-peptidic test compound is a small organic molecule.
30. The assay of claim 28, wherein said heterologous orphan G protein-coupled receptor is the human FPRL-1 receptor.
31. An assay for identifying a compound that modulates a heterologous receptor expressed by a yeast cell comprising:
i) providing a yeast cell which expresses a heterologous receptor which is functionally integrated into an endogenous yeast pheromone response pathway, wherein said yeast cell comprises an endogenous gene operatively linked to a heterologous promoter at the natural location of said endogenous gene to said yeast cell, said endogenous gene encoding a protease, and said promoter being responsive to signals produced by said pheromone response pathway;
ii) contacting the yeast cell with a test compound; and iii) detecting an alteration in a signal produced by the protease; to thereby identify a compound that modulates the heterologous receptor.
32. The assay of claim 31, wherein said promoter is non-naturally occurring.
33 The assay of claim 31, wherein said endogenous yeast gene is the BAR1 gene.
34. The assay of claim 31, wherein said promoter is naturally occurring.
35. The assay of claim 34, wherein the promoter is selected from the group consisting of the Fus1 promoter and the Fus 2 promoter.
36. An assay for identifying a compound that modulates a human FPRL-1 receptor expressed by a yeast cell comprising:
i) providing a yeast cull which expresses a human FPRL-1 receptor which is functionally integrated into an endogenous yeast signaling pathway;
ii) contacting the yeast cell with a non-peptidic test compound, and iii) detecting an alteration in a signal produced by the endogenous yeast signaling pathway;
to thereby identify a non-peptidic compound that modulates e human FPRL-1 receptor.
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JP2001501097A (en) 2001-01-30
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