IE84069B1 - Recombinant thrombin receptor and related pharmaceuticals - Google Patents

Description

RECOMBINANT THROMBIN RECEPTOR AND RELATED PHARMACEUTICALS THE REGENTS OF THE UNIVERSITY OF CALIFORNIA COR THERAPEUTICS, INC.

Technical Field The invention relates to materials involved in the control of the cardiovascular system, and in particular to activities mediated by thrombin and its cellular receptor. More specifically, it concerns recombinant materials useful for production of the thrombin receptor, use of the receptor as a diagnostic tool, and therapeutic agents which either stimulate or block thrombin receptor activation and diagnostic compositions relevant to the receptor.

Background Art Thrombin is a powerful factor in regulating the state of the cardiovascular system. It is clear that thrombin aids in the formation of blood clots by catalyzing the conversion of fibrinogen to fibrin, which is an integral part of most clots. In addition, thrombin is known to act directly on cells in the blood and in the interior blood vessel wall, and specifically to activate platelets to form clots. Thrombin-induced platelet activation is particularly important for arterial thrombus formation, a process that causes myocardial infarction and some forms of unstable angina and stroke.

In addition, thrombin promotes inflammation and other cellular activities. Thrombin is chemotactic for monocytes, mitogenic for lymphocytes, and causes endothelial cells to express the neutrophil adhesive protein GMP—l4O on their surfaces and inhibits the growth of these cells. Thrombin elicits platelet—derived growth factor from the endothelium and is a mitogen for mesenchymal cells.

Because thrombin is capable of direct activation of cells, it is assumed that at least one thrombin receptor exists. However, it has not been possible to detect the presence of thrombin receptor by traditional binding studies, since thrombin is capable of binding a large number of materials present on cells which do not directly mediate the cellular responses to thrombin, and thus the background levels of binding are prohibitively high. protease, if the receptor were proteolytically cleaved by (Gronke, et al., et al., the binding sites identified by since thrombin is a the interaction with thrombin, the receptor's ability to bind tightly to thrombin would be decreased. All of the foregoing factors suggest that traditional binding studies in an effort to find a thrombin receptor might ultimately be unproductive.

While it has been assumed that a thrombin receptor might exist, it has been unclear, even from the studies conducted so far, whether proteolytic cleavage by thrombin is involved in its receptor activation. When thrombin is treated with reagents which covalently modify and render it proteolytically inactive, its ability to stimulate platelets is abolished (Berndt, M.C., et al., "Platelets in Biology and Pathology" (1981) Elsevier/North Holland Biomedical Press, pp. 43-74; Martin, B.M., et al., Biochemistry (1975) ;g:1308-1314; Tollefsen, D.M., et al., J Biol Chem (1974) ggg:2646- 2651; Phillips, D.R , Thrombin Diath Haemorrh (1974) ;g:2o7-215; Workman, E.F., et al., J Biol Chem (1977) Some of thrombin-induced platelet activation and one modified nonproteolytic thrombin which does block platelet activation, D-phenylalanyl—L-prolyl—L-arginyl chloromethyl ketone (PPACK) thrombin fails to bind substrate. Thus, it cannot be concluded that a lack of protease activity accounts for failure to activate platelets.

The identification and characterization of the thrombin receptor, as described herein, permits the design of systems and substances which can regulate thrombosis in the cardiovascular system. In addition, new diagnostic reagents for assessing cardiovascular status are provided by this work.

Disclosure of the Invention We describe methods and materials useful in the regulation of the cardiovascular system in mammals. The isolation, recombinant production, and characterisation of the thrombin receptor associated with surfaces of cells activated by thrombin permits effective regulation of these functions. In accordance with the present invention, there is provided a DNA molecule encoding the human thrombin receptor having the amino acid sequence set forth in Figure 1 herein.

In one aspect, the invention is directed to recombinant materials associated with the production of thrombin receptor. In accordance with the present invention there is provided a DNA molecule comprising an expression system which when transformed into a recombinant host, produces human thrombin receptor at the cell surface of the host; wherein said expression system comprises a nucleotide sequence encoding the human thrombin receptor operably linked to a heterologous control sequence operable in said host, and wherein said thrombin receptor is encoded by a nucleotide sequence comprising a DNA molecule encoding the amino acid sequence of Figure 1 herein. The invention also relates to transfected cells, which contain the expression system of the invention, which can be cultured so as to display the thrombin receptor or their surfaces, and thus provide an assay system for the interaction of materials with native thrombin receptor. These cells, or peptides which represent relevant portions of the receptors, can be used as diagnostics to determine the level of thrombin in samples, as well as screening tools for candidate substances which affect thrombin activity ii_i_\/_i\/_o.

We also describe thrombin receptor agonists which mimic the activated form of the extracellular portion ofthe receptor protein. These agonists are useful in encouraging platelet aggregate formation, for example, in localized application at internal bleeding sites of hemophiliacs. The agonists also mimic thrombin’s ability to stimulate fibroblast poliferation and thus may be useful in promoting wound healing.

Tlirombin receptor antagonists are also described. These antagonists comprise modified forms ofthrombin receptor agonist peptides which lack the essential features required for activation of the receptor. These antagonists bind to receptor, do not activate it, and prevent receptor activation by thrombin.

A second group of compounds are described, that antagonize the action of thrombin are, in effect, thrombin inhibitors. receptor which would ordinarily represent cleavage and This group includes mimics of the thrombin-binding regions of the receptor, including noncleavable peptides and peptides with enhanced binding for thrombin. These peptides are capable of binding directly to thrombin so as to diminish the levels of thrombin capable of binding to receptor. They thus diminish or prevent thrombin—mediated events such as thrombin—induced platelet aggregation, fibrinogen clotting and cell proliferation.

A third group of compounds which behave as antagonists blocks the binding of thrombin to its receptor by providing alternate anionic regions to replace those of the thrombin receptor. These antagonists are mimics of the anionic region included in the thrombin-binding portion of the receptor. These antagonists also bind to thrombin, thereby preventing thrombin interaction with the intact receptor.

Conversely, alternate cationic regions which mimic those present in the thrombin ligand can be included in antagonists which occupy the binding region of the receptor and thus prevent binding of thrombin.

A fifth group of antagonists are described that include antibodies which are designed to bind specific regions of receptor protein. In general, these are monoclonal antibody preparations which are highly specific for any desired region of the thrombin receptor. The antibodies are also useful in immunoassays for the receptor protein, for example in assessingc successful expression of the gene in recombinant systems.

A sixth group of antagonists comprises modified forms of thrombin lacking proteolytic activity.

In another aspect, the invention is related to assay systems which utilize the hast cells of the invention displaying recombinant thrombin receptor to screen for agonists and antagonists. Some systems include the use of the agonist peptides to screen for antagonists which inhibit the agonistic effect.

These is also described diagnosis of cardiovascular disease by detection, in fluids such as blood or urine, of the peptide cleaved from the thrombin receptor when activated as a measure of thrombosis. Another diagnostic method is described including visualization of activated forms of receotor‘ and detecting" clots in the body’ by localizing and imaging these targets in situ using antibodies specific to the activated receptor.

Pharmaceutical compositions are also described containing the compounds described herein. The compounds which serve as antagonists to the activation of the thrombin receptor are useful as anti—thrombotics and are helpful in a variety of clinical indications including treatment of abrupt closure in the context of angioplasty, the treatment of restenosis in the context of angioplasty, the treatment of unstable angina, the treatment of myocardial infarction, and treatment of some forms of thrombotic or thromboembolytic stroke.

These compounds can be used alone or in combination with other therapeutic agents such as urokinase and tPA.

Brief Description of the Drawings Figure 1 shows the DNA and deduced amino acid sequence of a human thrombin receptor.

Figure 2 shows a proposed model of thrombin receptor activation based on the deduced amino acid sequence.

Figure 3 shows a comparison of amino acid sequences for the cleavage site and exosite binding domains deduced from the CDNA encoding human thrombin receptor and from the cDNA encoding murine thrombin receptor. Also shown is the relevant portion of the hirudin sequence.

Figure 4 shows platelet response to agonist peptide.

Figure 5 shows the mitogenic effect of an agonist peptide of the invention on fibroblasts.

Figures 6A, 6B and 6C show the effects of three thrombin inhibitor peptides on thrombin—induced platelet activation.

Figure 7 shows the effect of mutant thrombin on platelet ATP secretion stimulated by thrombin.

Figure 8 shows the increase in thrombin needed to overcome inhibition of platelet ATP secretion by mutant thrombin.

Figure 9 shows the effect of thrombin on platelet ATP secretion by varying concentrations of thrombin mutant.

Modes of Carrying Out the Invention The characteristics of the thrombin receptor elucidated by the invention herein are summarized in Figures 1 and 2. Figure 1 shows the complete DNA sequence of the clone encoding the receptor along with the deduced amino acid sequence. The entire amino acid sequence contains 425 amino acids, including a 24 or amino acid signal sequence which provides an approximately 400 amino acid mature receptor protein.

Hydrophobicity/hydrophilicity plots of the sequence shown in Figure 1 indicate that the mature receptor is a member of the 7-transmembrane domain receptor family and has a relatively long (approximately 75 amino acid) extracellular amino acid extension containing several consensus sites for asparagine-linked glycosylation. A disulfide bond linking cysteine—175 in the first extracellular loop with cysteine-254 in the second extracellular loop would be analogous to rhodopsin and B-2 adrenergic receptor. A proposed model of the in situ receptor is shown in Figure 2.

Referring again to Figure 1, the thrombin- catalyzed cleavage site is represented by the Arg-Ser linkage at positions 41 and 42. Cleavage at this site results in the liberation of a peptide fragment of the receptor designated an "activation peptide" extending from position 1 of the mature peptide to the cleavage site. The precise processing site of the receptor is not known and thus the N-terminus of the mature protein is somewhat uncertain. However, it is probably the arginine residue at position 28. The "activation peptide" would thus have the sequence RPESKATNATLDPR. location of the N-terminus is unimportant for the design The precise of the compounds described below. This "activation peptide“ is likely to be freely filtered by the kidney and possibly concentrated in the urine, and can be used as an index to platelet activation by thrombin.

The amino acid sequence destined to be cleaved by thrombin--i.e., the cleavage site--binds to thrombin's active site/"oxyanion hole" region which is contained in an extended binding pocket. This oxyanion hole binds large substrates via hydrophobic, hydrogen bonding, and charge interactions. Typically, the sequence to be cleaved interacts with the amino acids of the active site, while sequences carboxyl to this cleavage site interact with the more extended "anion binding exosite." The thrombin receptor contains the anionic sequence YEPFWEDEE at positions 52-60, as shown in Figure 1. This region is just carboxyl to the cleavage site between positions 41 and 42. The location and the composition of this YEPFWEDEE sequence (aromatic/hydrophobic residues and anionic residues) strongly suggest that this sequence contains regions that mediate thrombin binding to the receptor via thrombin's anion-binding exosite. This hypothesis is confirmed hereinbelow by showing that peptides representing at least a portion of this region of the receptor bind thrombin and inhibit its actions.

This observation also predicts that polycationic substances that bind to this portion of the receptor may block thrombin binding and receptor activation.

Release of the activation peptide permits refolding of the receptor protein to activate the receptor. This is shown schematically in Figure 2, which also shows that the conformational changes resulting from the liberation of the activation peptide and refolding results in an intracellular conformational change of the receptor. This hypothesis is confirmed by the finding that the thrombin receptor can be activated by a peptide mimicking the new amino terminus created by the activation. Accordingly, mimics of the N-terminus of the new amino terminus on the activated receptor behave as agonists therefor. The importance of the first two amino acids in the newly created amino terminus in the receptor for receptor activation has also been confirmed hereinbelow. Switching the positions of the amino terminal serine and phenylalanine results in complete loss of agonist activity for the above agonist peptides.

Based on this information, and by analogy with the mechanisms underlying trypsinogen activation to trypsin, it appears that the positively charged amino group on serine that is newly exposed when thrombin cleaves the receptor plays an important role in receptor activation.

Peptides based on the agonist peptide sequence that bind the thrombin receptor but are modified to be lacking the a—amino group can function as antagonists of the thrombin receptor. Thus, modifications of the agonist peptides which lack the capacity for specific activating interaction serve as thrombin receptor antagonists.

Compounds The nomenclature used to describe the peptide compounds follows the conventional practice where the N-terminal amino group is assumed to be to the left and the carboxy group to the right of each amino acid residue in the peptide. In the formulas representing selected specific embodiments of the present invention, the amino- and carboxy-terminal groups, although often not specifically shown, will be understood to be in the form they would assume at physiological pH values, unless otherwise specified. Thus, H+2 and C—terminal O" at physiological pH are understood the N-terminal to be present though not necessarily specified and shown, either in specific examples or in generic formulas. Free functional groups on the side chains of the amino acid residues can also be modified by amidation, acylation or change the other substitution, which can, for example, solubility of the compounds without affecting their activity.

In the peptides shown, each gene-encoded residue, where appropriate, is represented by a single letter designation, corresponding to the trivial name of the amino acid, in accordance with the following conventional list: Amino Acid Alanine Arginine Asparagine Aspartic acid Cysteine Glutamine Glutamic acid Glycine Histidine Isoleucine Leucine Lysine Methionine Phenylalanine Proline Serine Threonine Tryptophan Tyrosine Valine One-Letter Three—letter Symbol S o1 Ala Arg Asn Asp Cys Gln Glu Gly His Ile Leu Lys Met Phe Pro Ser Thr Trp Tyr Val < +< 2 +3 m 'u H: 3 :2 t'r4 m an m (3 0 t3 2 as v The amino acids not encoded genetically are abbreviated as indicated in the discussion below.

In the specific peptides shown in the present application, the L-form of any amino acid residue having an optical isomer is intended unless the D—form is expressly indicated by a dagger superscript (T).

The compounds described herein are peptides which are partially defined in terms of amino acid residues of designated classes.

Amino acid residues can be generally subclassified into four major subclasses as follows: Acidic: The residue has a negative charge due to loss of H ion at physiological pH and the residue is attracted by aqueous solution so as to seek the surface positions in the conformation of a peptide in which it is contained when the peptide is in aqueous medium at physiological pH.

Basic: The residue has a positive charge due to association with H ion at physiological pH and the residue is attracted by aqueous solution so as to seek the surface positions in the conformation of a peptide in which it is contained when the peptide is in aqueous medium at physiological pH.

Neutral/nonpolar: The residues are not charged at physiological pH and the residue is repelled by aqueous solution so as to seek the inner positions in the conformation of a peptide in which it is contained when the peptide is in aqueous medium. These residues are also designated "hydrophobic" herein.

Neutral/polar: The residues are not charged at physiological pH, but the residue is attracted by aqueous solution so as to seek the outer positions in the conformation of a peptide in which it is contained when the peptide is in aqueous medium.

It is understood, of course, that in a statistical collection of individual residue molecules some molecules will be charged, and some not, and there will be an attraction for or repulsion from an aqueous medium to a greater or lesser extent. To fit the definition of "charged," a significant percentage (at of the individual molecules are The degree of attraction or least approximately 25%) charged at physiological pH. repulsion required for classification as polar or nonpolar is arbitrary and, therefore, amino acids specifically contemplated herein have been classified as one or the other. Most amino acids not specifically named can be classified on the basis of known behavior.

Amino acid residues can be further subclassified as cyclic or noncyclic, and aromatic or nonaromatic, self—explanatory classifications with respect to the side chain substituent groups of the residues, and as small or large. The residue is considered small if it contains a total of 4 carbon atoms or less, inclusive of the carboxyl carbon. Small residues are, of course, always nonaromatic.

For the naturally occurring protein amino acids, subclassification according to the foregoing scheme is as follows.

Acidic: Aspartic acid and Glutamic acid; Basicznoncyclicz Arginine, Lysine; Histidine; Basiczcyclicz Neutral olar small: Glycine, serine, cysteine; Neutral non olar small: Alanine; Neutralzpolarzlargeznonaromatic: Threonine, Asparagine, Glutamine; Neutral/Dolar/large aromatic: Tyrosine; Neutral/nonDolar/larqe/nonaromatic: Valine, Isoleucine, Leucine, Methionine; Neutralznonpolarzlargezaromatic: Phenylalanine, and Tryptophan.

The gene—encoded secondary amino acid proline, although technically within the group neutral/nonpolar/large/ cyclic and nonaromatic, is a special case due to its known effects on the secondary conformation of peptide chains, and is not, therefore, included in this defined group.

Certain commonly encountered amino acids, which are not encoded by the genetic code, include, for example, beta-alanine (beta-Ala), or other omega—amino acids, such as 3-amino propionic, 4-amino butyric and so forth, alpha-aminisobutyric acid (Aib), sarcosine (Sar), ornithine (Orn), citrulline (Cit), t-butylalanine (t—BuA), t-butylglycine (t—BuG), N-methylisoleucine (N—MeIle), phenylglycine (Phg), and cyclohexylalanine (Cha), norleucine (Nle), cysteic acid (Cya) 2- naphthylalanine (2-Nal); 1,2,3,4-tetrahydroisoquinoline- 3-carboxylic acid (Tic); B—2—thienylalanine (Thi); and methionine sulfoxide (MSO). These also fall conveniently into particular categories.

Based on the above definitions, Sar and beta—Ala and Aib are neutral/nonpolar/ small; t-BuA, t-EuG, N-MeIle, Nle, Mvl and Cha are neutral/nonpolar/large/nonaromatic; Orn is basic/noncyclic; Cya is acidic; Cit, Acetyl Lys, and MSO are neutral/polar/ large/nonaromatic; and Phg, Nal, Thi and Tic are neutral/nonpolar/large/ aromatic.

The various omega—amino acids are classified according to size as neutral/nonpolar/small (beta-Ala, i.e., 3-aminopropionic, 4-aminobutyric) or large (all others).

Other amino acid substitutions of those encoded in the gene can also be included in peptide compounds and can be classified within this general scheme according to their structure.

All of the compounds described herein, when an amino acid forms the C-terminus, may be in the form of the pharmaceutically acceptable salts or esters. Salts may be, for example, Na+, K+, Ca”, Mg” and the like; the esters are generally those of alcohols of l—6C.

A. Agonists The agonists described below comprise a series of peptides of the formula A155‘-AA}/'(AAi)n‘Z (1) wherein AAX is a small amino acid or threonine, preferably selected from ser, ala, gly and, and thr and AAY is a neutral/nonpolar/aromatic amino acid residue or is a neutral/nonpolar/large/nonaromatic amino acid containing a cyclic portion (preferably a neutral/ nonpolar/aromatic amino acid residue); wherein AA represents an amino acid residue and the subscript i is an integer which denotes the position of the referent amino acid residue downstream (N+C) of the AAY residue of formula (1), and n is an integer of 2-12, with the proviso that if n=2, Z must comprise an amidated C terminus of the formula NR'R' wherein at least one R’ is alkyl containing at least one polar substituent; and in general, Z is a noninterfering substituent.

AA1 and AA2 must, therefore, be present in the AAl and AA2 are relatively precisely defined; however AA3-AA12 compounds of formula 1; AA3-AAl2 are optional. are, generally, L—amino acid residues. The position of AAI is also relatively tolerant; therefore, AAl is a neutral or basic amino acid having a free a=amino group in the L—configuration; AA2 is a neutral or basic L-amino acid residue; and AA3-AAIZ are L—amino acid residues, wherein preferably AA3 is a basic or neutral amino acid residue; AA4 and AA6 are each independently neutral/polar/large/nonaromatic amino acids or AA4 may be a basic amino acid; AA5 and AAll are each independently proline or small amino acid residues; AA7 and AAlO are each independently acidic amino acid residues; AA8 is a basic amino acid residue; and AA9 and AAl2 are each independently neutral/ aromatic amino acid residues.

The peptide of formula 1 can be extended (shown as included in Z) at the C—terminus (but not the N- terminus) by further amino acid sequence to comprise a noninterfering substituent.

At the C-terminus of the compounds of formula 1, the carboxyl group may be in the underivatized form or may be amidated; in the underivatized form the carboxyl may be as a free acid or a salt, preferably a pharmaceutically acceptable salt.

If the C-terminus is amidated, the nitrogen atom of the amide group, covalently bound to the carbonyl carbon at the C—terminus, will be NR’R’, wherein each R’ is independently hydrogen or is a straight or branched chain alkyl of l—6C, such alkyls are 1-6C straight— or branched-chain saturated hydrocarbyl residues, such as methyl, ethyl, isopentyl, n—hexyl, and the like.

Representatives of such amido groups are: —NH2, -NHCH3, _l7_ -N(CH3)2, -NHCHZCH3, —NHCH2CH(CH3)2, and -NHCH2CH(CH3)CH2CH3, among others. Furthermore, either or both R’ may in turn optionally be substituted by one or more substituents such as, for example, -OR’, —NR’R', -NR’CNR’NR'R’ and the like, wherein each R’ is as Thus, Z may be -OH (or an halo, independently defined above. ester or salt form), or -NR'R' wherein R’ defined. is as above Preferred embodiments of AAX-AAY include GF, AF, sp, TF, G(pClPhe), A(pClPhe), S(pClPhe), T(pClPhe), GThi, AThi, SThi, and TThi. Preferred embodiments of AAl and AA2 are large nonpolar amino acids. embodiments for the residues in the remainder of the Preferred compound of formula (1) are those wherein AAI and AA2 are each independently Leu, Val, Ile, Cha, Phe, 2-Nal or Tic; or AA3 is Arg, Lys, Orn, Har or Ala. For the remaining amino acids, preferred are embodiments wherein AA4 and AA6 are each independently Gln, Asn or Lys; or AA7 and AAIO are each independently Asp or Glu; AA8 is Arg or Lys; or AAl2 is Phe and AA9 is Tyr; or Z is OH, or NR’R’ wherein R’ is as defined above; or Z further includes some or all of AAI3-AA17 as defined below. preferred are compounds of formula (1) which are selected from the group consisting of SFLLRNPNDKYE; SFLLRNPNDK; SFLLRNPN; SFLLRNP; SFLLRN; SFLLR; GFLLR; TFLLRNPNDK; S(pClPhe)LLR; S(Thi)LLR; SFFLR; SFFLRN; SF(Phg)LR; sFL(Na1)RN; SFL(Cha)R; SF(Cha)(Cha)RN; SF(Cha)(Cha)RK; SF(Cha)(Cha)LRNPNDK; SFLLKN; SFLL(Har)N; SFLLKN; SFF(Cha)AN; and the amidated forms thereof.

Particularly B. Antagonists Compounds described below which interfere with platelet activation and other cellular activities mediated by the thrombin receptor include the following: ) Antagonists for the thrombin receptor which represent modified agonist peptides lacking the N- terminal serine residue; 2) Thrombin inhibitors which represent noncleavable and/or enhanced binding forms of the extracellular portions of the thrombin receptor which behave as decoys for the circulating thrombin; ) Anionic and hydrophobic/anionic peptides which mimic at least a portion of the YEPFWEDEE anionic- binding exosite region and which also behave as decoys for circulating thrombin; ) Cationic or extended cationic peptides which mimic the anionic—binding exosite of thrombin itself and bind to the receptor in competition with thrombin; ) Antibodies which are immunoreactive with various critical positions on the thrombin receptor; and ) Thrombin mutants lacking proteolytic activity which compete with native thrombin for the receptor.

Thrombin Receptor Antagonists The antagonists of the first group--modified agonists—-can be represented by the formula: X-AAY-(AAi)n-Z (2) wherein X is an amino acid residue other than Ser, Ala, Thr, Cys or Gly or is a desamino or N—acylated amino acid; AAY is a neutral nonpolar large amino acid residue containing a cyclic portion, preferably aromatic; AA represents an amino acid residue and the subscript i is an integer which denotes the position of the referent amino acid residue downstream (N+C) of the AAY residue of formula (2) and n is an integer of 4-12; and wherein AA1 and AA2 are each independently neutral or basic L—amino acid residues wherein AAl has a free a-amino group; neutral amino acid residues; and AA8 are each independently basic or AA4 and AA6 are each independently basic or nonaromatic amino acids; AA5 and AA1l residues or small amino acids; AA7 amino acid residues; AA9 and AAl2 are each independently neutral/ aromatic amino acid residues; and are each independently proline and AAlO are each independently acidic Z is a noninterfering substituent.

Preferred embodiments of X include residues of 3-mercaptopropionic acid (Mpr), 3—mercaptovaleric acid (Mvl), 2-mercaptobenzoic acid (Mba) and S-methyl—3— mercaptopropionic acid (SMeMpr).

Preferred embodiments for this group of anti- thrombin activity compounds include those wherein AAl and AA2 are each independently Leu, Val, Ile, Phe, Cha, 2—Nal or Tlc; or AA3 and AA8 are each independently Arg, Lys, Orn or Har; or AA4 and AA6 are each independently Lys, Arg, Orn, Har, Gly, Gln or Asn; or AA5 and AA1l are each independently Pro or Ala; or AA7 and AAlO are each independently Asp, Glu, B-Asp or 3-Glu; or AAl2 is Phe and AA9 is Tyr; or Z is OH (or an ester or salt form), NH2, or NR'R’ wherein each R’ is independently H or straight- or branched-chain alkyl of 1—6C optionally substituted as described above.

Particularly preferred embodiments are those peptides wherein X is Mpr, S-Me Mpr or Mba, AAY is Phe, AAl is Cha, and AA2 is Cha.

Particularly preferred are embodiments of AAl- AA2 can each independently be Cha. which are encoded by the gene, or wherein AAl and Particularly preferred among the antagonist peptides of this class are those selected from the group consisting of XFLLRNPNDKYEPF; XFLLRNPNDKYEP; XFLLRNPNDKYE; XFLLRNPNDKY; XFLLRNPNDK; XFLLRNPND; XFLLRNPN; XFLLRNP; XFLLRN; XFLLR; XFLL; XFL; X-F(Cha)(Cha)RNPNDK, X-F(Cha)(Cha)RNPNDKY, XF(Cha)(Cha)RNPNDKYE—NH2, X-F(Cha)(Cha)RNPNDKY-NH2, X- F(Cha)(Cha)RNPNDK-NH2, X-F(Cha)(Cha)RNPND-NH2, X—F(Cha)(Cha)RN-NH2, X-F(Cha)(Cha)RAPNDK-NH2, X-F(Cha)(Cha)RGPNDK-NH2, X—F(Cha)(Cha)RKPNDK-NH2, X—F(Cha)(Cha)RNANDK-NH2, X-F(Cha)(Cha)RNPADK-NH2, X-F(Cha)(Cha)RNPNDA-NH2, X—F(Cha)(Cha)RKPNEK-NH2, and X-F(Cha)(Cha)RKPNDA-NH2; especially wherein X is Mpr.

Especially preferred are Mpr-F(Cha)(Cha)RNPNDK, Mpr—F Cha (Cha)RNPNDKY, Mpr—F(Cha)(Cha)RNPNDKYE-NH2, Mpr—F Cha (Cha)RNPNDKY—NH2, Mpr-F(Cha)(Cha)RNPNDK-NH2, C Mpr—F Cha (Cha)RAPNDK-NH2, Mpr-F(Cha)(Cha)RGPNDK—NH2, Mpr-F Cha (Cha)RKPNDK-NH2, Mpr—F(Cha)(Cha)RNANDK—NH2, Mpr-F(Cha)(Cha)RNPADK-NH2, Mpr-F(Cha)(Cha)RNPNDA-NH2, Mpr-F(Cha)(Cha)RKPNEK—NH2, Mpr-F(Cha)(Cha)RKPNDA-NH2, Mba-F(Cha)(Cha)RKPNDK-NH2, and SMeMpr—F(Cha)(Cha)RKPNDK— NH2.

( ) ( ) Mpr—F( ha)(Cha)RNPND-NH2, Mpr-F(Cha)(Cha)RN-NH2, ( ) ( ) Thrombin Inhibitors The thrombin inhibitors of group 2) compounds that bind thrombin in competition with receptor but are noncleavable and/or exhibit enhanced binding These compounds are of the formula: represent properties.

J-AAy-(AAi)n-AA9-AA1O-AA1l-AA12-AAl3-z <3) wherein J is a peptide extension of 2-5 amino acid residues or an acylated or desamino form thereof.

In the compounds of formula (3), as above, AAY is a neutral nonpolar large amino acid residue containing a cyclic portion, preferably aromatic; and n is 8.

As above, AA represents an amino acid residue and the subscript i is an integer denoting position downstream from AAY.

As above, AAl and AA2 are each independently neutral or basic amino acid residues; AA3 and AA8 are each independently neutral or basic amino acid residues; AA4 and AA6 are each independently basic or neutral nonaromatic amino acids; AA5 and AAll are each independently proline residues or small amino acids; AA7 and AAlO are each independently acidic amino acid residues; AA9 and AAl2 are each independently neutral/ aromatic amino acid residues; AA is an aromatic or small nonpolar amino acid residue; and Z is a noninterfering substituent.

For these thrombin inhibitors which are of group (2) above, wherein the peptide mimics the thrombin receptor extracellular chain but lacks a proteolytic site and/or has enhanced binding for thrombin, particularly preferred embodiments are those which include downstream anionic amino acid residues and wherein J is a peptide extension of 4-5 amino acid residues. Particularly preferred are those wherein the residues immediately upstream of AAY have the sequence pro-arg-pro (PRP) preceded by residues selected from the group consisting of dipeptide sequences consisting of a large/nonaromatic/nonpolar/neutral amino acid residue conjugated through a peptide bond to an acidic amino acid residue downstream. Particularly preferred embodiments of this dipeptide sequence are ile—asp, val-asp, ile- glu, and leu—asp, especially wherein said peptide extension represented by J is selected from the group consisting of LDPRP, LEPRP, IDPRP, IEPRP, VDPRP and VEPRP.

In addition, where the peptide extension includes the immediately upstream sequence pro-arg-pro, an additional preferred upstream further extension is a D amino acid. Particularly preferred are D amino acids which are large/nonpolar/neutral/aromatic, particularly tryptophan or phenylalanine, and in particular phenylalanine.

Z is preferably OH (or an ester or salt form) or NR’R’, where R’ is defined as above, which may optionally be preceded by a peptide extension mimicking the receptor sequence downstream from AAl3.

Particularly preferred compounds of formula (3) are peptides which are selected from the group consisting of LDPRPFLLRNPNDKYEPFWEDEEKNES; LDPRPFLLRNPNDKYEPFWEDEEKNE; LDPRPFLLRNPNDKYEPFWEDEEKN; LDPRPFLLRNPNDKYEPFWEDEEK; LDPRPFLLRNPNDKYEPFWEDEE; LDPRPFLLRNPNDKYEPFWEDE; and LDPRPFLLRNPNDKYEPFWED, and the amidated or acylated forms thereof. Also preferred are those which are selected from the group consisting of FTPRPFLLRNPNDKYEPFWEDEEKNES, FTPRPFLLRNPNDKYEPFWEDEEKNE, FTPRPFLLRNPNDKYEPFWEDEEKN, FTPRPFLLRNPNDKYEPFWEDEEK, FTPRPFLLRNPNDKYEPFWEDEE, FfPRPFLLRNPNDKYEPFWEDE, and FTPRPFLLRNPNDKYEPFWED; and FTPRPFLLRNPNDKYEPFWEDEEKNES, FTPRPFLRNPNDKYEPFWEDEEKNES, FTPRPFRNPNDKYEPFWEDEEKNES, FTPRPFNPNDKYEPFWEDEEKNES, FTPRPFPNDKYEPFWEDEEKNES, FTPRPFNDKYEPFWEDEEKNES, FTPRPFDKYEPFWEDEEKNES, FTPRPFKYEPFWEDEEKNES, FTPRPFYEPFWEDEEKNES, and FTPRPFEPFWEDEEKNES, and the amidated and acylated forms thereof.

Anion Exosite-Binding Antagonists Antagonists which represent peptides mimicking the binding region of the receptor, YEPFW, optionally including the anionic extension (EDEE) thereof (group 3), are represented by the formula: B—AA9—AA1O—AA1l—AAl2-AA13—Z (4) wherein AA9, AAl2 and AAI3 are each, independently, neutral aromatic or small amino acid residues, AAlO is an acidic amino acid residue, AAl1 is proline or a small amino acid residue; and wherein B and Z are noninterfering substituents, typically peptide extensions, but can also include noninterfering organic radicals in general. B can also be H or acyl (including said peptide extension if present); Z may also be OH (or an ester or salt form thereof) or NR'R'(also including said peptide extension if present), as set forth hereinabove.

Preferred forms of compounds of formula (4) are those wherein each of AA9, AA12 and AA13 is phe, trp, ala or tyr; and AAIO is glu, asp, 6-glu or B-asp.

Particularly preferred are embodiments wherein AA9—AAl3 is YEPFW, FEPFW, YDPFW, YEPYW, YEPFY, YEPWY or WEPFW. Z may include the peptide sequence EDEE, QDQQ, EDEQ, QDEQ, QDEE, EDQE, EDQQ or QDQE.

Preferred embodiments of B include those wherein B is H or a peptide extension of 1-4 amino acids or the acylated form thereof.

These antagonists serve as decoys for thrombin, thus lowering its effective concentration.

Anionic-Binding Exosite Mimics The cationic peptides mimicking a portion of the anionic-binding exosite of thrombin (group 4) are of the formula: B-AAa-AAb-AAC-AAd—AAe—Z (5) wherein B and Z are defined as above, and wherein AAa and AAe are each independently hydrophobic amino acids or basic amino acids, and where each of AAb, AAC, and AAd is independently a basic amino acid.

Preferred are compounds of formula (5) wherein B comprises acyl or H; or Z comprises OH (or an ester or salt) or NR'R’ wherein each R’ is defined as above; or AAa and AAe are each independently selected from phe, trp and ala; or AAb-AAd are each independently selected from the group consisting of arg, lys and gln; especially wherein AAa-AAe has the sequence WKKKK, KKKKW, QKQQW, or WQKQQ.

The noninterfering substituents represented by B and Z may be further peptide extensions which are compatible with the binding pattern of the thrombin anionic-binding exosite. As they mimic this capacity of thrombin to bind its substrate, these antagonists are operative by virtue of their ability to bind the relevant regions of the thrombin receptor protein, and, in particular, the region YEPFWEDEE at positions 52-60, as shown in Figure 1.

Antibodies Antagonists which are antibodies immunoreactive with critical positions of the thrombin receptor (group 5) are obtained by immunization of suitable mammalian subjects with peptides containing as antigenic regions those portions of the thrombin receptor intended to be targeted by the antibodies. Critical regions include the region of proteolytic cleavage, the binding site at the YEPFWEDEE box, the segment of the extracellular segment critical for activation (this includes the cleavage site), and the portions of the sequence which form the extracellular loops, in particular, that region which interacts with the N- terminus of the activated receptor extracellular region.

The agonist peptides of the invention may be used as immunogens in this case.

Thus, suitable peptides to use as immunogens to prepare the desired antibodies include those peptides representing portions of the mature sequence of the extracellular region from positions 28 to position 68, at the C—terminal end of the YEPFWEDEE region. This region has the sequence: PESKATNATLDPRSFLLRNPNDKYEPFWEDEEKNESGLTEY and peptides which include the sequence LDPRSFLL (which includes the cleavage site) and YEPFWEDEE (which includes the binding site) are particularly useful. Alternative regions which are useful as immunogens include the segment representing amino acids 161-176; 240-265; and 336-346. These peptides of the sequences, respectively, YYFSGSDWQFGSELCR, KEQTIQVPGLNITTCHDVLNETLLEG, and HYSFLSHTSTT, represent the proposed extracellular loops.

The antibodies are prepared by immunizing suitable mammalian hosts in appropriate immunization protocols using the peptide haptens alone, if they are of sufficient length, or, if desired, or if required to enhance immunogenicity, conjugated to suitable carriers.

Methods for preparing immunogenic conjugates with carriers such as BSA, KLH, or other carrier proteins are well known in the art. In some circumstances, direct conjugation using, for example, carbodiimide reagents may be effective; in other instances linking reagents such as those supplied by Pierce Chemical Co., Rockford, IL, may be desirable to provide accessibility to the hapten. The hapten peptides can be extended at the amino or carboxy terminus with a Cys residue or interspersed with cysteine residues, for example, to facilitate linking to carrier.

Administration of the immunogens is conducted generally by injection over a suitable time period and with use of suitable adjuvants, as is generally understood in the art. During the immunization schedule, titers of antibodies are taken to determine adequacy of antibody formation.

While the polyclonal antisera produced in this way may be satisfactory for some applications, for pharmaceutical compositions, use of monoclonal preparations is preferred. Immortalized cell lines which secrete the desired monoclonal antibodies may be prepared using the standard method of Kohler and Milstein or modifications which effect immortalization of lymphocytes or spleen cells, as is generally known. The immortalized cell lines secreting the desired antibodies are screened by immunoassay in which the antigen is the peptide hapten or is the thrombin receptor itself displayed on a recombinant host cell. When the appropriate immortalized cell culture secreting the desired antibody is identified, the cells can be cultured either in gitgg or by production in ascites fluid.

The desired monoclonal antibodies are then recovered from the culture supernatant or from the ascites supernatant. Fragments of the monoclonals or the polyclonal antisera which contain the immunologically significant portion can be used as antagonists, as well as the intact antibodies. Use of immunologically reactive fragments, such as the Fab, Fab’, of F(ab’)2 fragments is often preferable, especially in a therapeutic context, as these fragments are generally less immunogenic than the whole immunoglobulin.

The antibodies or fragments may also be produced, using current technology, by recombinant means.

Regions that bind specifically to the desired regions of receptor can also be produced in the context of chimeras with multiple species origin.

Noncleavable Thrombin In addition to the foregoing, antagonists comprise thrombin mutants lacking proteolytic activity that compete with native thrombin for the receptor (group 6). As set forth above, it is understood that the participants in the proteolytic cleavage site of thrombin include the serine residue at B-chain position 205, the histidine residue at position 57, and the aspartic acid residue at position 99. Mutants of thrombin containing replacements for these residues which render the thrombin molecule proteolytically inactive are prepared using standard site-directed mutagenesis techniques, and the mutant genes used to produce the modified thrombin using recombinant techniques. The relevant substitutions are denoted by the position number preceded by the native residue and followed by the substituted residue. Thus, thrombin with serine at position 205 replaced by alanine is denoted S205A.

Preferred Embodiments In both the agonists and antagonists of groups (1) — (4), some of the preferred embodiments of the amino acid sequences are those wherein the amino acid in the peptides are those encoded by the gene.

Also included are those wherein one, two, three or more of the amino acid residues is replaced by one which is not encoded genetically.

In more detail, for these preferred embodiments, preferred embodiments of AAl and AA2 are leu, val, or ile; especially preferred is leu. Preferred embodiments of AA3 and AA8 are arg or lys; especially preferred are embodiments wherein AA3 is arg and AA8 is lys. Preferred embodiments for AA4 and AA6 are gln or asn, and especially asn. Preferred embodiments for AA7 and AA1O are asp or glu; particularly preferred are embodiments wherein AA7 is asp and AAIO is glu. A preferred embodiment for AA12 is phenylalanine, and of AA9 is tyrosine.

Preferred acyl groups are of the formula RCO- wherein R represents a straight or branched chain alkyl of 1—6C. Acetyl is particularly preferred.

In all of the peptides described, one or more amide linkages (-CO-NH-) may optionally be replaced with another linkage which is an isostere such as —CH2NH—, -CHZS-, —CH2CH2, —CH=CH- (cis and trans), —COCH2—, -CH(0H)CH2- and -CHZSO-. be made by methods known in the art.

This replacement can The following references describe preparation of peptide analogs which include these alternative-linking moieties: Spatola, A.F., Vega Data (March 1983), Vol. 1, Issue 3, "Peptide (general review); Morley, J.S., cis and trans); (~COCH2-); Jennings—White, C., et al., Tetrahedron Lett (1982) ;;:2533 (—COCH2-); Szelke, M., et al., Application E? 45665 (1982) CA:21:39405 (1982) (—CH(OH)CH2—); Holladay, M.W., et al., Tetrahedron Lett (1983) 2_ Ci (1982) ;;:l89-199 (-CH2-S-).

European Preparation of Peptide Agonists and Antagonists The peptide agonists and antagonists described herein can be prepared using standard solid phase (or solution phase) peptide synthesis methods, as is known in the art. In addition, the DNA encoding these peptides may be synthesized using commercially available oligonucleotide synthesis instrumentation and produced recombinantly using standard recombinant production systems. The production using solid phase peptide synthesis is necessitated if non—gene-encoded amino acids are to be included.

Recombinant Production of Thrombin Receptor The invention provides recombinant materials for the production of thrombin receptor for display on the surface of recombinant cells. Production of the receptor using these recombinant methods provides a useful diagnostic reagent either to determine the level of thrombin in biological samples or, more importantly, as a reagent to screen candidate substances which affect thrombin activity.

For this recombinant production, a DNA sequence encoding the thrombin receptor, as set forth in Figure 1, or its degenerate analogs is prepared either by retrieval of the native sequence, as set forth below, or by using substantial portions of the known native sequence as probe, or can be synthesized de novo using standard The DNA is ligated into expression vectors procedures. suitable for the desired transformed host and transformed into compatible cells. The cells are cultured under conditions which favor the expression of the thrombin receptor encoding gene and the cells displaying the receptor on the surface harvested.

Use of Recombinant Thrombin Receptor as a Diagnostic and Screening Tool The availability of the recombinant DNA encoding thrombin receptor permits expression of the receptor on host cell surfaces, thus making the cells available as a tool for evaluating the ability of candidate agonists or antagonists to bind to receptor.

In one type of easily conducted assay, competition of a candidate antagonist for binding to the receptor with either labeled thrombin, a thrombin agonist The labeled substance known to bind the receptor can, of course, be a or known binding antagonist can be tested. synthetic peptide. Varying concentrations of the candidate are supplied along with a constant concentration of labeled thrombin, thrombin agonist, or antagonist, and the inhibition of a binding of label to the receptor can be evaluated using known techniques.

In a somewhat more sophisticated approach, the effect of candidate compounds on thrombin—induced responses can be measured in the cells recombinantly expressing the thrombin receptor as described below.

Assay systems for the effect of thrombin on these cells include calcium mobilization and voltage clamp which are further described in detail hereinbelow. other suitable endpoints include thrombin-induced phosphoinositol turnover and inhibition of adenyl cyclase. These assays permit an assessment of the effect of the candidate antagonist on the receptor activity rather than simply ability to bind to thrombin.

Diagnosis of Cardiovascular Disease In one embodiment, the availability of the recombinant thrombin receptor protein permits production of antibodies which are immunospecific to the activated form of the receptor which can then be used for diagnostic imaging of activated receptors in yigg. These antibodies are produced either to the activated form of the receptor produced recombinantly, or to the peptide representing the "new amino terminal" peptide described in Example 2 below. The resulting antibodies, or the immunospecific fragments thereof, such as the Fab, Fab’, Fab'2 fragments are then conjugated to labels which are detected by known methods, such as radiolabels including technetium and indium or other radioactive labels as is known in the art. When injected in yiyg, these antibodies home to the sites of activated receptor, thus permitting localization of problem areas which are subject to thrombosis.

In another embodiment of diagnosis, the presence of the activation peptide in body fluids can be detected and measured. Antibodies are made to the activation peptide as described above and can be employed in standard ELISA or RIA assays to detect excess amounts of the activation peptide in, for example, urine.

Utility and Administration of Antagonists The antagonists described herein are useful therapeutically in the treatment of abrupt closure or restenosis in the context of angioplasty; in the treatment of unstable angina; and in the treatment of myocardial infarction. The peptides which behave as antagonists may be administered in conventional formulations for systemic administration as is known in the art. Typical such formulations may be found, for example, in Remington's Pharmaceutical Sciences, Mack Publishing Co., Easton PA, latest edition.

Preferred forms of systemic administration of peptides include injection, typically by intravenous injection. other injection routes, such as subcutaneous, intramuscular, or intraperitoneal, can also be used.

More recently, alternative means for systemic administration of peptides have been devised which include transmucosal and transdermal administration using penetrants such as bile salts or fusidic acids or other detergents. In addition, if properly formulated in enteric or encapsulated formulations, oral administration may also be possible.

The dosage range required depends on the choice of antagonist, the route of administration, the nature of the formulation, the nature of the patient’s illness, and the judgment of the attending physician. Suitable dosage ranges, however, are in the range of 0.1-100 pg/kg of subject. Wide variations in the needed dosage, however, are to be expected in view of the variety of antagonists available and the differing efficiencies of various routes of administration. For example, oral administration would be expected to require higher dosages than administration by intravenous injection.

Variations in these dosage levels can be adjusted using standard empirical routines for optimization as is well understood in the art.

The agonists described herein are useful in the treatment of wounds and in other contexts wherein fibroblast proliferation is useful. Administration of these compounds is generally topical and/or localized, in the form of salves, pastes, gels and the like.

Assay Systems Various assay systems may be used to measure the interaction of thrombin with its receptor and the affect of various candidate agonists and antagonists thereon. The role of the thrombin receptor and thrombin in platelet aggregation can be measured directly by aggregometry or the effect on blood clotting involving In addition, ATP uptake Also useful as a measure __—_——_é_..:._...

In this assay, washed Charo, induce aggregation, approximately 1-20 nM thrombin or ECSO of an alternate agonist is used to stimulate aggregation in control reactions; the results are followed by lumiaggregometry. Candidate agonists at various concentrations may be used in place of thrombin to stimulate aggregation. Candidate inhibitors are added to the reaction mixture in addition to the thrombin in order to assess their ability to prevent aggregation.

Washed platelets are suspended in modified Tyrode's buffer, pH 7.4 with 2 mM magnesium and 1 mM calcium at a concentration of 108 platelets/ml. The thrombin or test compound is added in a small volume (about 20 uL) in 600 mM NaCl, 10 mM MES pH 6.0, 0.5% PEG 6000 buffer and incubated for 15 minutes at 37°C with a platelet suspension.

Platelet Activation/ATP Secretion: prepared as above in 480 pl of suspension are added to 20 Platelets pl of phosphate buffered saline containing sufficient thrombin to give a final concentration of about 10 nM, or About 20 pl Chromolume® reagent (Chronolog Corporation, Havertown, an alternate agonist is added at its ECSO.

PA) is added. In addition to measuring aggregation, ATP secretion is assessed. These results quantitated independently measuring changes in luminescence and light transmittance in a chronolog dual channel Platelet ATP secretion is measured in a lumiaggregometer as lumiaggregometer (chronolog Corporation). luminescence signal. Candidate antagonists which putatively interact with thrombin are preincubated with the thrombin in 20 pl PBS at room temperature for 5 minutes before addition to the platelets. Preincubation is not necessary for testing agonists or antagonists which interact directly with the receptor.

Platelet Aggregation Assav Usinq Microtiter Plates: Thrombin- or agonist-mediated platelet aggregation as measured with washed platelets in 96-well microtiter plates was performed as described (Fratantoni, J.C. et al., Am J Clin Pathol (1990) gg:613—617). The ability of hybridoma supernatants, purified MoAbs or peptide antagonists to block the thrombin receptor was assessed in this assay with various concentrations of antibodies or antagonists.

Fibrinoqen Clotting Assay: Fibrinogen clotting reactions are performed in a total volume of 300 pl in 150 mM NaCl, 20 mM Tris, pH 7.4, 10 mM CaCl2, 0.5% PEG 6000 at 37°C and a final fibrinogen concentration of 3.3 mg/ml. Thrombin at 5 nM gives an approximately second clotting time as measured by a standard Fibrosystem@ coagulation timer (Fisher Scientific, Springfield, NJ).

As described above, candidate agonists are used in place of the thrombin to stimulate fibrant formation; oocytes are washed, then incubated in MESH II without Briefly, intracellular calcium antibiotics for 90 minutes. Groups of 5 oocytes are selected and placed in individual wells in a 24-well tissue culture plate (Falcon 3047) containing 0.5 ml/well MSH II without antibiotics. This medium is removed and replaced with fresh medium every 10 minutes; the harvested medium is analyzed by scintillation counting to determine 45Ca released by the oocytes during each 10- minute incubation. The 10-minute incubations are continued until a stable baseline of 45Ca release per unit time is achieved. Two additional 10-minute collections are obtained, then test medium including agonist is added and agonist-induced 45Ca release determined.

Voltage Clamp: currents are measured in voltage-clamped oocytes expressing thrombin receptor encoding CRNA essentially as previously described (Julius, D., et al, Science (1988) 241:558-563) except that the single electrode voltage- Agonist-induced inward chloride clamp technique is employed.

The following examples are intended to illustrate but not to limit the invention.

Example 1 Preparation of CDNA Encoding Thrombin Receptor In summary, the human cell lines HEL (Papayannopoulou, T., et al., J Clin Invest (1987) 1g:859-866) and Dami cells (Greenberg, S.M., et al., glppg (1988) 1g:1968-1977) were stimulated with phorbol 12-myristate 13-acetate (PMA) before isolation of mRNA for microinjection into Xenopus oocytes. The oocytes which had been injected with these mRNA samples were then assayed for cellular calcium mobilization to detect those eggs which were expressing the thrombin receptor encoded by the RNA at their surfaces. the mRNA, a 40 kb mRNA fraction was used for preparation After size selection of of a cDNA library. The library was assayed by conversion of plasmid DNA, cloned in E. coli, into capped CRNA in an in vitro system, and injection of the capped CRNA into the oocytes. An insert in a positive clone was sequenced to obtain the CDNA and deduced amino acid sequence shown in Figure 1. penicillin, 100 pl/ml streptomycin, and 50 ug/ml A Practical gentamicin).

Dumont stage V oocytes were selected and microinjected with 50 ml of the mRNA to be tested (1 pg/pl in 10 mM Hepes, pH 7.0); 5 ng of CRNA transcribed from a cDNA encoding a secreted form of alkaline phosphatase (generously provided by Dr. S. Udenfriend) was coinjected with all mRNA or cRNA samples as an internal standard for selection of healthy oocytes (Tate, s.s., et al., FASEB J (1990) 3:227-231). oocytes were cultured for 48 h at 18°C in MESH II in Microinjected individual wells in 96-well culture plates; the oocyte- conditioned medium was then assayed for alkaline phosphatase activity as described (Tate et al., (supra)) and the "best-expressing" oocytes were selected for functional assays.

Cytoplasmic and poly A+ RNA were prepared from HEL and Dami cells by standard techniques (Sambrook, J., et al., Molecular Cloning, 1989, Cold Spring Harbor Laboratory Press, New York). Poly A+ RNA was fractionated by size by centrifugation through a 10-30% sucrose density gradient exactly as described by Sumikawa, K., et al., Nucl Acids Res (1982) ;g:5809- 5822. Aliquots of each gradient fraction were analyzed for size by glyoxal gel electrophoresis. of each fraction was twice ethanol precipitated, and RNA dissolved at 1 pg/pl in 10 mM Hepes, pH 7.0. each fraction were assayed in the oocyte system described The remainder Aliquots of above for thrombin receptor activity. the rare cutter Mlul next to the NotI site. pFROG placed the cDNA under the transcriptional control of the SP6 RNA polymerase promoter and directed the synthesis of a hybrid mRNA containing the 5’—untranslated region of Xenopus globin followed by message encoded by the cDNA insert.

All pools were screened using both the voltage clamp and 45Ca release assay. Of the first five pools screened, all showed some thrombin receptor activity; in the 45Ca release assay, thrombin-induced increases in 45Ca release ranged from two— to six-fold. The most active pool was replated at approximately 2000 clones per plate and rescreened in the oocyte system. Two of 10 pools screened were positive for thrombin receptor activity. The most active of these was replated at 300 clones per plate and the pools rescreened. By progressive selection and subdivision of active pools, a single clone was identified.

The 3480-nucleotide cDNA insert was subcloned into the XhoI site of pBluescript. Restriction fragments of the insert were subcloned into M13. The cDNA sequence was determined twice in each direction (three times for the coding region) by dideoxy sequencing. The results are shown in Figure 1.

Figure 1 shows both the nucleotide sequence and the deduced amino acid sequence for the thrombin receptor protein. Hydrophobic regions, including a putative signal sequence and seven transmembrane spans are After processing of the signal sequence by it is probable that additional overlined. signal peptidase, processing by proline-directed arginyl cleavage occurs between the arginines at positions 27 and 28, which is marked on the Figure. Thus, mature protein begins RPESK.... the amino terminus of the Possible asparagine— linked glycosylation sites are underlined, and consensus polyadenylation regions are in bold. The putative thrombin receptor cleavage site at position R41/S42 is also marked.

As set forth above, Figure 2 provides a diagram of the disposition of the thrombin receptor in the cell membrane. As shown in Figure 2, the amino terminal extracellular extension of the intact and unactivated thrombin receptor is cleaved by thrombin, exposing a new amino terminus and releasing the short receptor fragment designated the "activation peptide" herein. The newly exposed amino terminus then functions as an agonist, Vbinding to an as yet undefined region of the thrombin receptor and activating it. The thrombin receptor is thus activated by a mechanism analogous to zymogen-enzyme conversion. Thus, the thrombin receptor, like other receptors which contain seven transmembrane regions, contains its own ligand with the N-terminus in the native form of S42/F43.

The availability of the human cDNA encoding thrombin receptor permitted the retrieval of the corresponding murine form. A high degree of homology is shown at the cleavage site and anion exosite binding domain. The homology of these sequences with each other and with the anion exosite binding domain of hirudin is shown in Figure 3.

Example 2 Synthesis of Ser-Phe-Leu—Leu-Arq-Asn-NH2 (SFLLRN-NH2_)_ Starting with paramethylbenzhydrylamine resin - HCl (0.5 mmol synthesis, 0.77 meq/g, Applied Biosystems, Foster City, CA) was subjected to neutralization with diisopropylethylamine (DIEA) in N—methylpyrolidinone (NMP), followed by washings and addition of the required amino acids coupled as 1-hydroxybenzotriazole esters and introduced in order using an Applied Biosystems 431A peptide synthesizer. The Boc-amino acids had the following sidechain protection: Ser (OBzl) and Arg (Tos). achieved with HF/anisole/methylethylsulfide (56/6/1 (v/v)) to afford the crude peptide which was purified by Cleavage of the completed peptide resin was C18 reversed-phase liquid chromatography using a gradient of acetonitrile in water containing 0.1% trifluoroacetic acid (TFA).

Example 3 Agonist Activity of a "New Amino-Terminal" Peptide On Oocvtes Expressing Wild-Tvpe and Mutant Thrombin Receptor cRNA Oocytes were microinjected with 5 ng wild—type thrombin receptor CRNA (WT) or with 5 ng cRNA encoding a mutant thrombin receptor with the amino acid substitution R4lA (R4lA). thrombin as set forth above——alanine replaces arginine at position 41. Uninjected oocytes or oocytes expressing thrombin receptor cRNAs were then cultured for 48 hr and thrombin or peptide—induced 45Ca release determined as The notation is analogous to that for described above. Candidate agonists were added at saturating concentrations: thrombin at 250 pM and the "new amino-terminal" peptide SFLLRNPNDKYEPF (SFLL peptide) at 25 pM. The control peptide FSLLRNPNDKYEPF (FSLL peptide) was added at 100 pM and elicited no response. The data shown in Table 1 represent the mean +/- SEM of three replicate determinations; these results are representative of those obtained in three or four separate experiments.

Table 1 Fold increase Receptor Aqonist in 45Ca WT Thrombin 26 WT "SFLL" peptide 40 pM 32 WT "SFLL" peptide 200 pM 42 R4lA Thrombin 0 1241A "SFLL" peptide 200 pM 53 The agonist SFLL peptide has no activity on uninjected oocytes (not shown). Qualitatively identical results were obtained when agonist-induced inward current in voltage-clamped oocytes was used as an endpoint rather than agonist-induced Ca release.

Example 4 Agonist Function of the "New Amino-Terminal" Peptide for Platelet Secretion and Aggregation and Mitogenic Effects Washed human platelets were prepared as described by Baenzinger, N.G., Meth Enz (1974) ;;:149— 155; and Charo, I.F., et al., J Clin Invest (1977) Platelet aggregation in response to 1, 10, 20, 100 or 200 pM peptide SFLLRNPNDKYEPF "SFLL" peptide or to nM thrombin was measured in a lumiaggregometer, and Agonist-induced responses were assessed as the results are shown in Figure 4A.

Platelet ATP secretion in response to the indicated final concentrations of "new amino-terminal“ peptide was also followed by lumiaggregometry, and the results are shown in Figure 4B.

The data shown in Figure 4 are raw tracings representative of aggregation or secretion responses obtained in triplicate for each agonist concentration, and are representative of results obtained in more than five separate experiments. 100% aggregation is arbitrarily defined as that occurring in response to a saturating concentration of thrombin at one minute. 100% secretion is arbitrarily defined as the maximal response occurring in response to a saturating concentration of thrombin. The “new amino terminal" peptide is comparably active to 20 pM thrombin at concentrations of 100 pM in both assays as shown in the figure. The control peptides FSLLRNPNDKYEPF and LLRNPNDKYEPF were both without activity at concentrations as high as 200 pM (not shown).

In an additional determination, the mitogenic effects of the agonist peptide were demonstrated using CCL-39 cells. The fibroblast cell line CCL—39 was made quiescent in serum-free medium and then treated for 48 hours with the candidate agonist in the presence of tritiated thymidine. The incorporation of label into DNA was then determined as TCA-insoluble activity, shown as cpm in Figure 5 using standard techniques. The data shown in the figure represent the mean of six replicate determinations plus or minus 95% confidence.

The agonists Shown in the figure were: None (serum—free); % fetal bovine serum (10% FCS); nM a-thrombin (a-T); , 10 or 100 pM agonist peptide of the sequence SFLLRNPNDKYEPF (NTP); pM "scrambled" agonist peptide, which is the foregoing with the N—terminus scrambled to FS (FSLL).

As shown in Figure 5, the NTP at 100 uM gives significant stimulation of growth. Merely switching the positions of the first two residues of the agonist caused loss of activity. Thus, the agonist peptide not only simulates platelet aggregation, but also is useful in stimulating fibroblast proliferation, which is useful in wound—healing applications.

Platelet Aqqreqation Aqonists: Using the platelet aggregation assay described above, the concentration of various peptides required to elicit a 50% maximal aggregation was determined. The values obtained, shown as ECSO, are shown in Table 2 in micromolar units.

Table 2 Agonist Peptides Peptide SFLLRNPNDKYE 6 6 SFLLRNPNDK 6 3 SFLLRNPN 7 6 SFLLRNP-NH2 4.5 SFLLRN-NH2 l 6 SFLLR—NH2 7 5 SFLL-NH2 146 Ac-SFLLRNPNDYKE Ac-FLLRNPNDKYEPF FLLRNPNDKYEPF Edesaminoserl-FLLR-NH2 [desaminoAsn]-FLLR—NH2 [nethythioacetyll-FLLR-NH2 [3-Tetrahydrofuranoyll-FLLR-NH2 S(N-MePhe)LLRNPNDKYE DFLLR-NH2 KFLLR-NH2 FFLLR-NH2 [Acm-Cys]-FLLR—NH2 [Va1ery1]-FLLR—NH2 [2-MeButyry1]-FLLR-NH2 Edesaminoornl-FLLR—NH2 [N-MeSer]-FLLRNPNDKYE [D-Ser]—FLLRNPNDKYE CFLLR-NH2 (S-MeCys)FLLRN—NH2 [b-Ala]-FLLR-NH2 GFLLR-NH2 TFLLRNPNDK AFLLRNPNDKYE SALLRNPNDKYE S(D-Phe)LLRNPNDKYE SLLLR—NH2 ‘ SYLLR-NH2 S(NO2Phe)LLR-NH2 S(homoPhe)LLR-NH2 S(Phg)LLR-NH2 S(Tic)LLR-NH2 S(Cha)LLR-NH2 S(Na1)LLR—NH2 S(OMeTyr)LLR-NH2 S(pC1Phe)LLR-NH2 Inactive 796 Inactive 920 237 366 Inactive Inactive Inactive Inactive WA 2000 1500 WA 850 172 193.0 129.2 99 7.3 8.5 12.9 Inactive Inactive Inactive 288 250 Inactive Inactive Inactive 140 42 46 8 . 44. 45. 46. 47. 48. 49. 50. 51. 52. 53. 54. 55. 56. 57. 58. 59. 60. 61. 62. 63. 64. 65. 66. 67. 68. 69. 70. 71. 72. 73. 74. 75. 76. 77.

S(Thi)LLR—NH2 SF(D-Leu)LRNPNDKYE SF(D-A1a)LR—NH2 SF(b-A1a)LRN-NH2 SF(Aib)LRN-NH2 SFDLR-NH2 SF(N-MeLeu)LR-NH2 SFHLRN-NH2 SFALRNPNDKYE SFWLR-NH2 SFFLR-NH2 SFFLRN-NH2 SF(Phg)LR-NH2 SFPLR-NH2 SFGLR—NH2 SFRLR-NH2 SFYLRN-NH2 SFILR—NH2 SF(Cha)LR—NH2 SF(Cha)LRN—NH2 SF(Tic)LRN-NH2 SFL(D-Leu)RNPNDKYE SFLARNPNDKYE SFLPR-NH2 SFLER-NH2 SFLAR-NH2 SFLQRN-NH2 SFLIRNfNH2 SFLFR-NH2 SFLRR-NH2 SFL(Na1)RN-NH2 SFL(Cha)R—NH2 SF(Cha)(Cha)RN—NH2 SF(Cha)(Cha)LRNPNDK SFLLDN—NH2 .6 Inactive Inactive Inactive Inactive Inactive >1000 . SFLL(D-Arg)—NH2 594 79. SFLLA-NH2 137 80. SFLLLN-NH2 44_9 81. SFLLQN—NH2 2o_2 82. SFLLKN—NH2 11_1 83. SFLLHarN-NH2 3_3 84. SFF(Cha)RA-NH2 1.4 85. SF(Cha)(Cha)RK-NH2 , 0.82 Example 5 Inhibition of Thrombin-Induced Platelet Activation by Thrombin Inhibitor Peptides Three antagonist peptides, LDPRPFLLRNPNDKYEPFWEDEEKNES (LDPRP peptide), FTPRPFLLRNPNDKYEPFWEDEEKNES (FTPRP peptide) and LDPRPFLL (shortened LDPRP peptide), were tested for their ability to inhibit thrombin-induced platelet activation.

Thrombin was incubated with the candidate inhibitory peptide for 5 minutes, then the mixture was added to washed platelets and platelet activation was followed as platelet ATP secretion by lumiaggregometry. The mixtures were added in a total volume of 20 #1 phosphate buffered saline to 480 #1 of platelets prepared and suspended as described in the description under the heading "Assays" hereinabove. Various concentrations of the candidate peptides were used. The results are shown in Figures 6A, 6B and 6C. The ATP secretion is expressed as a percentage of the mean luminescence signal generated by nM thrombin in the absence of the candidate peptides; the figures shown are representative of the results of three replicate experiments.

Figure 6A shows the results for the LDPRP peptide, which shows an IC5O of approximately 500 nM.

The LDPRP peptide contains sequences which are representative of both the cleavage site and the putative thrombin binding site. Figure 6B shows the results obtained for the shortened LDPRP peptide; the ICSO is now approximately 200 uM.

However, as shown in Figure 6C, the FTPRP peptide which contains an alternate form of the putative cleavage site as well as the putative binding site has an ICEO of approximately 200 nM; this peptide is thus a more effective antagonist than either the LDPRP peptide or its shortened form.

Example 6 Preparation of Thrombin Receptor Antagonist Peptide: Synthesis of Mpr-Phe-Cha—Cha—Arq~Asn-Pro—Asn—Asp—LVs—OH Starting with N—a-Boc—e-(Cl-CBZ)—Lys—O—Pam— Resin (0.5 mmol, 0.70 meq/g, Applied Biosystems, Foster City, CA), the Boc group was removed with TFA, neutralized, washed and the required amino acids were added in sequence by coupling as l—hydroxybenzotriazole esters employing an Applied Biosystems 431A peptide synthesizer. The peptide was cleaved from the resin and purified by reversed—phase chromatography as described in Example 3.

Candidate peptides analogously synthesized were tested in the platelet activation/aggregation assays described above and added at various concentrations in the presence of thrombin. The concentration which resulted in 50% inhibition of activation or aggregation was designated the ICSO and is shown for the various peptides tested in Table 3 in micromolar units.

Table 3 Antaqonist Activity Mpr—FLLRNPNDK Mpr—FLLRNPNDKYE—NH2 Mpr-FLLR—NH2 Mpr-FLLRC—NH2 Mpr-FLLRNC-NH2 Mpr-FLLRNPNC-NH2 Mpr-F(Cha)(Cha)RNPNDK Mpr-F(Cha)(Cha)RNPNDKY Mpr-F(Cha)(Cha)RNPNDKYE-NH2 Mpr—F(Cha)(Cha)RNPNDKY-NH2 Mpr—F(Cha)(Cha)RNPNDK—NH2 Mpr—F(Cha)(Cha)RNPND-NH2 Mpr-F(Cha (Cha)RN-NH2 ) Mpr—F(Cha)(Cha RAPNDK—NH2 Mpr—F(Cha)(Cha RGPNDK—NH2 Mpr-F(Cha)(Cha RFPNDK-NH2 Mpr—F(Cha)(Cha RKPNDK—NH2 ( Mpr-F(Cha) Cha RNANDK-NH2 Mpr—F(Cha)(Cha RNPADK—NH2 Mpr—F(Cha)(Cha)RNPNAK—NH2 Mpr-F(Cha)(Cha)RNPNDA-NH2 Mpr-F(Cha)(Cha)RKPNEK-NH2 Mpr-F(Cha)(Cha)RKPNDA-NH2 [SMe-Mpr]-FLLR-NH2 [Cam-Mpr]-FLLR-NH2 Mvl-FLLR-NH2 Pivaloyl-FLLR-NH2 (SMeMpr)—F(Cha)(Cha)RKPNDK—NH2 (2-Mba)-F(Cha)(Cha)RKPNDK-NH2 Mpr-F(Cha)(Cha)RKPND-OH -400 500-1000 500-1000 As shown in Table 3, substitution of the amino acid Cha for the leucine and Lys for Asn residues improves the antagonist activity.

Example 7 Generation of Active-site Thrombin Mutants After confirmation by DNA sequencing, DNA determined by ELISA and Western blots and the highest yielding clones were grown to confluence in a 24,000 cm2 surface cell "factory" (Nunc, Inter Med, Naperville, IL) in MEM a-nucleoside—deficient medium with 80 nM methotrexate, 100 units/ml penicillin, 100 pg/ml streptomycin, 25 mM Hepes buffer, 5 pg/ml vitamin K, 0.2 mg/ml proline, and 10% dialyzed bovine calf serum.

Upon reaching full confluence, all medium was removed, all growing surfaces washed six times with phosphate- buffered saline to remove contaminating bovine prothrombin and thrombin, and cells were grown in MEM a-nucleoside—deficient medium containing 100 units/ml penicillin, 100 pg/ml streptomycin, 25 mM Hepes buffer, pg/ml vitamin K, 0.2 mg/ml proline, 1 pg/ml insulin and pg/ml transferrin for 36-48 hours.

Conditioned medium was cleared of cellular debris by centrifugation and filtration, diluted 1:1 with water, made to 10 mM Tris-HCl, pH 7.4, and 20 mM citrate (final concentration) and stirred overnight at 4°C with 1% (v/v) S—Sepharose beads were removed by centrifugation and the conditioned medium was refiltered (V/V) Q-Sepharose was then collected in a 10 ml column and eluted in 1 ml fractions with 600 mM NaCl, 10 mM Tris- HCl, pH 7.4, 0.5% PEG 6000 and positive fractions containing recombinant prothrombin identified by Western S-Sepharose. and stirred overnight at 4°C with 1% Q—Sepharose. blot using anti—human thrombin antiserum. pH was then changed to 7.0 ,000-fold molar excess of (p-amidinophenyl)- methanesulfonyl fluoride (APMSF) to inhibit Factor Xa and any bovine thrombin that might contaminate the preparation. APMSF is a serine—dependent irreversible thrombin antagonist that rapidly inactivates native thrombin at pH 7.0 but has a half-life of only 10'3 sec at pH 8.0. For this reason, the pH of the APMSF-treated mutant thrombin preparation was then changed to 8.0 for min to eliminate all APMSF.

The mutant thrombin-containing solution was then changed to pH 6.0 by addition of 1N HCl and stirred (V/V) S—Sepharose was collected in a 10 ml column, washed with 150 mM Nacl. 10 mM MES. pH 6.0 and subsequently eluted with 600 mM NaCl, 10 mM MES, pH 6.0, 0.5% PEG 6000 in Positive fractions were identified by V€rni9ht at 4°C with 1% S—Sepharose. The ml fractions.

Western blot with anti—human thrombin antiserum and the concentration and purity of recombinant S205A or D99N/S205A thrombin preparations were determined by Coomassie and silver-stained SDS-PAGE gels. The mutant thrombin preparations used in these studies appeared homogeneous on silver—stained SDS-PAGE gels.

Example 8 Fibrinogen Clotting Assay Fibrinogen clotting activity was measured by a standard Fibro System“ coagulation timer (Fisher Scientific, Springfield, NJ) as the time required for varying thrombin concentrations to generate a fibrin clot. All fibrinogen clotting reactions were performed in a total volume of 300 pl, in 150 mM NaCl, 20 mM Tris, pH 7.4, 10 mM CaCl2, 0.5% PEG 6000 at 37°C with a final fibrinogen concentration of 3.3 mg/ml. Both standard WT and recombinant WT showed identical curves—-e.g., about second clotting times at 5 nM. Neither S2OSA nor D99N/S205A were able to induce clotting.

Example 9 Platelet ATP Secretion and Aggregation Studies Washed platelets were prepared as described above and suspended in modified Tyrode' buffer, pH 7.4 with 2 mM magnesium and 1 mM calcium at a concentration of 108 platelets/ml. All platelet studies were performed in a total volume of 500 #1 with 20 pl Chromolume® Platelet reagent (Chronolog Corporation, Havertown, PA).

ATP secretion and aggregation were quantitated independently by measuring changes in luminescence and light transmittance, respectively, in a Chronolog dual- channel lumiaggregometer (Chronolog Corporation, Havertown, PA). Platelets were stirred at 300 rpm to ensure rapid and uniform distribution of agonist. 500 pl of platelets were incubated for 15 minutes at 37°C with 18 pl of diluted S205A stock in 600 mM NaCl, 10 mM MES, pH 6.0, 0.5% PEG 6000 buffer to give the desired final concentrations, or 18 #1 of buffer alone and then challenged with native thrombin (1 mM final concentration). Platelet ATP secretion and aggregation were followed for 30 seconds after thrombin addition. percentage of maximum, defined as the luminescence signal Platelet ATP secretion data are expressed as a obtained 30 seconds after addition of 1 mM native thrombin to buffer—pretreated platelets. The results are shown in Figure 7. Each point represents the mean of three replicate determinations, and are representative of three replicate experiments. As shown, increasing concentrations of S205A thrombin cause increasing inhibition of thrombin-induced platelet secretion.

Similar results were obtained using the D99N/S205A mutant thrombin.

In an additional determination it was shown (Figure 8) that 400 nM SZOSA thrombin right-shifts the dose response of platelets to native thrombin by approximately 1 log. In this determination, 18 pl of S205A in 600 mM NaCl, 10 mM MES, pH 6.0, 0.5% PEG 6000 buffer to give a final S205A concentration of 400 nM) or an equal volume of buffer alone (solid lines) were incubated with 500 pl of platelets for 15 minutes at 37°C. final concentrations of a—thrombin; platelet ATP Platelets were then stimulated with the indicated secretion and aggregation were followed for 30 seconds after thrombin addition. The date shown reflect the maximum initial rate of platelet ATP secretion, specifically, the maximum rate of platelet ATP secretion occurring within 30 seconds of agonist addition and before any aggregation was detected. Thus, the platelet ATP secretion rates reported represent only agonist- induced and not aggregation-induced responses. Curves from three replicate experiments are shown in Figure 5.

One arbitrary unit corresponds to 33 pmoles of ATP released per second based on calibration with ATP standards.

An additional experiment shows S205A thrombin inhibits the extent of native thrombin—induced platelet secretion. Platelets were preincubated with various concentrations of S205A, then stimulated with native thrombin (1 nM final concentration). To prevent aggregation-induced secretion, platelets in these experiments were suspended to a final concentration of 2 x 107 platelets/ml and were not stirred after the addition of native thrombin. Under these conditions, platelets did not aggregate but did secrete ATP in response to thrombin. Platelet secretion rate is expressed in arbitrary units as defined above. Figure 9 shows tracings of platelet secretion curves, and are representative of the results obtained in three replicate experiments. The decrease in luminescence seen in the control curve (0 nM S205A thrombin) is characteristic of the assay and may represent end—product inhibition of luciferase.

However, S205A thrombin does not inhibit ATP secretion induced in platelets by stimulation with agonist peptide or a calcium ionophore.

Example 10 Preparation of Antibodies The peptides representing portions of the thrombin receptor amino terminal extension were used as immunogens to prepare polyclonal antisera and monoclonal antibodies.

The peptide PESKATNATLDPRSFLLC (the cleavage site peptide) and the peptide YEPFWEDEEKNESGLTEYC (the anion exosite domain peptide) were used to generate antibodies. These antisera were tested as antagonists in the platelet activation assay described above. Both were effective in blocking activation. The polyclonal antibody preparation which is immunoreactive with the anion exosite domain peptide, AblO47, was incubated with the platelets prior to the addition of thrombin at a 1 nM concentration was added. The inhibition was reversed by the addition of the peptide binding Ab1047, 360." Ab1047 at a 1:100 dilution almost completely inhibits the aggregation and activation of the platelets.

The peptide PESKATNATLDPRSFLLRNPNDKYEPFWEDE EKNESGLTEC which contains the cleavage site and the "peptide proposed anion binding exosite of the receptor was also used to prepare potent receptor blocking monoclonal antibodies. This 40 residue peptide which has a Cys residue added at the carboxyl terminus of the native sequence was covalently attached to keyhole limpet hemocyanin (KLH) through the Cys residue using the thiol- specific reagent, m-maleimidobenzoyl-N-hydroxysulfo— succinimide ester (Sulfo-MES, Pierce Chemical Co.).

Following dialysis of the peptide-KLH conjugate, this material was used to immunize 3 BALB/c mice. Spleen cells obtained from each of the mice were fused with P3X cells to form a panel of hybridomas.

Supernatants from these hybridomas were assayed for their ability to crossreact with the native residue peptide used for the immunization as well as 15- residue peptides which span the length of the 40-residue sequence in ELISA assays. Only IgG-specific clones were investigated further. Positive hybridomas were then tested for their ability to block thrombin-induced platelet aggregation in the microtiter plate shaker assay. Finally, positive hybridomas were reassayed with the ELISA assay using the 40-residue peptide under increasing salt washing conditions to choose 6 hybridomas with apparent high affinity. The 6 hybridomas were subcloned by limiting dilution resulting in clones 4-2, -6, 31-2, 33-1, 61-1, and 62-5.

Each of the clones was used for the production of ascites fluid by intraperitoneal injection of 1 x 107 cells/mouse cells. Ascites fluid rich in IgG was purified on protein A—sepharose, as the therapeutic The ability of each of these purified monoclonal antibodies to inhibit thrombin-induced platelet aggregation (using thrombin as agonist) was evaluated in washed platelets and is shown in Table 5. The IC5Os for these MoAbs ranged between .5-20 yg/ml of purified IgG. potential of IgG is greater than IgM.

Table 5 Inhibition of Platelet Aqqreqation by Antibodies LQSO fggzml Washed MoAb Platelets) 4-2 10-20 -6 >20 31-2 2.5-5.0 33-1 2.5-4.0 61-1 2.5-5.0 62-5 10-20

Claims (1)

1. A DNA molecule comprising a nucleotide sequence encoding the human thrombin receptor, said thrombin receptor having the amino acid sequence set forth in