WO1983002447A1

WO1983002447A1 - Antigenic linear peptide compounds

Info

Publication number: WO1983002447A1
Application number: PCT/US1982/000004
Authority: WO
Inventors: University Northwestern; Erwin Goldberg
Original assignee: Northwestern University
Current assignee: Northwestern University
Priority date: 1982-01-04
Filing date: 1982-01-04
Publication date: 1983-07-21
Anticipated expiration: 1984-07-04
Also published as: EP0101677A4; EP0101677A1; EP0101677B1; DE3271909D1; AU8089182A; ATE20669T1

Abstract

Les nouveaux composés de peptides linéaires antigéniques de cette invention comprennent des séquences de 9 à 14 acides aminés qui comprennent la séquence 9-amino acide: ariginine-méthionine, valine-sérine-glycine-glutamine, thréonine-arginine-leucine, tous les acides aminés à l'exception de la glycine étant sous leur forme en L. Les composés sont utiles dans des vaccins réduisant la fertilité chez les mammifères.The novel antigenic linear peptide compounds of this invention include 9 to 14 amino acid sequences which include the 9-amino acid sequence: ariginine-methionine, valine-serine-glycine-glutamine, threonine-arginine-leucine, all amino acids with the exception of glycine being in their L-form. The compounds are useful in vaccines reducing fertility in mammals.

Description

ANTIGENIC LINEAR PEPTIDE COMPOUNDS

BACKGROUND AND PRIOR ART

Mammalian spermatozoa have been known to be antigenic for many years. More recently, it has been demonstrated that mammalian sperm contain an antigenic enzyme, which is known as the C, isozyme of lactate dehydrogenase (LDH-X, LDH-C,) . LDH-C, has been isolated in pure crystalline form from mouse testes. Goldberg (1972) J. Biol. Chem. 247:2044-2048. The enzyme has a molecular weight of 140,000 and is composed of four identical C sub- units. The amino acid sequence and three-dimen¬ sional structure of LDH-C 4, has been studied and partially^' determined by a number of investigators. See Musick et al (1976) J. Mol. Biol. 104:659-668; and Wheat et al (1977) Biochem. ^'& Biophys. Res. Com . , 74, No. 3:1066-1077. Wheat et al determined the sequence of the essential thiol peptide from amino acid 159 to 171, and found this to be nearly identical to essential thiol peptides from other vertebrate LDH isozymes. In 1974, Dr. Erwin Goldberg reviewed the effects of immunication with LDH-X (LDH-C,) on fer¬ tility, and advanced the possibility that "by using a defined macromolecular constituent of sperm it becomes possible to elucidate its primary structure in terms of amino acid sequence, to map specifical¬ ly the antigenic determinant(s) responsible for in-

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OMPI ducing infertility, and then to construct synthetic peptides containing these determinants. Possessing the capability for synthesizing a molecule with such properties, makes the immunological approach to fertility control feasible." Karolinska Sympo¬ sia on Research Methods in Reproductive Endocrinol- gy, 7th Symposia: Immunological Approaches to Fer¬ tility Control, Geneva, 1974 202-222. However, such synthetic antigenic peptides remained a goal and not achievement, although their theoretical desirability has been recognized. In 1979, Dr. Erwin Goldberg summarized the state of the art as follows:

"In conclusion, and on a practical basis, immunotherapy for birth control requires more than effectiveness, specificity, reversibil¬ ity, and absence of systemic side reaction. Rather large amounts of the antigen must be available in unequivocally pure form. This condition probably cannot be met by a natu¬ ral product enzyme antigen from sperm or testes. Rather, contraceptive technology requires a synthesizable peptide fragment retaining antigencity and provoking a re- • sponse which impairs fertility. Completion of the structural analysis of LDH-C, should allow mapping of antigenic determinants and synthesis of such peptides for use in a new contraceptive technology." "Recent advances in Reproduction and Regulation of Fertility," G.P. Talwar, editor, Elsevier/North Holland Biomedical Press (1979)

SUMMARY OF INVENTION

It has now been discovered that antigenic peptides can be prepared by synthesizing a linear sequence of 9 to 14 amino acids including the se¬ quence: - arginine-methionine-valine-serine-glycine- glutamine-threonine-arginine-leucine. All of the amino acids used to prepare these peptide compounds are in their L-form with the exception of glycine. The arginine is at the N-terminal and the leucine is at the C-terminal, or in the C-terminal end por¬ tion. Although not known with certainty, it is be¬ lieved that the foregoing sequence of nine amino acids corresponds to amino acids 101 to 109 of LDH-C, . This is contrary to a recently published tentative sequence. Musick et al (1979) J. Biol. Chem. , 254, No. 16: 7621-7623. The other compounds respectively are believed to correspond to the 101-111, 101-112, 101-113, 101-114, and 101-115 se¬ quence of LDH-C,, contrary to Musick et al. In the sequence numbering convention used, there is no amino acid 104.

DESCRIPTION OF INVENTION The present invention relates to novel antigenic linear peptides having chain length from 10 to 14 amino acids. These peptides all include the N-terminal sequence:

N-Arg-Met-Val-Ser-Gly-Gln-Thr-Arg-Leu More specifically the invention generical- ly comprises the following five peptide compounds.

(P-l) N-Arg-Met-Val-Ser-Gly-Gln-Thr-Arg-Leu-C,

(P-2) N-Arg-Met-Val-Ser-Gly-Gln-Thr-Arg-Leu-Asp-C,

(P-3)' N-Arg-Met-Val-Ser-Gly-Gln-Thr-Arg-Leu-Asp- Leu-C,

(P-4) N-Arg-Met-Val-Ser-Gly-Gln-Thr-Arg-Leu-Asp- Leu-Leu-C,

(P-5) N-Arg-Met-Val-Ser-Gly-Gln-Thr-Arg-Leu-Asp- Leu-Leu-Gln-C, and (P-6) N-Arg-Met-Val-Ser-Gly-Gln-Thr-Arg-Leu-Asp- Leu-Leu-Gln-Arg-C, wherein the letter "N" designates the N-terminal amino acids, while the letter "C" designates the

C-terminal amino acids. Gly represents glycine, and Arg, Met, Val, Ser, Gin, Thr, Leu, and Asp re-

OMPI spectively represent the L-amino acid forms argi- nine, methionine, valine, serine, glutamine, threo- nine, leucine, and aspartic acid.

The peptide compounds of the present in- vention P-l, P-2, P-3, P-4, P-5, and P-6 can be synthesized from their constituent amino acids. For example, the synthesis can be carried out by the Merrifield solid phase method, as described in J.A.C.S. 85:2149-2154 (1963). This solid phase method for synthesizing -sequences of amino acids is also described in Stewart and Young, Solid Phase Peptide Synthesis (W. H. Freeman and Co. , San Fran¬ cisco, 1969), pages 1-4. In this procedure, the C- terminal amino acid, such as arginine for the P-l compound of this invention is attached to chloro- methylated polystyrenedivinylbenzene copolymer beads. Each subsequent amino acid, with suitable protecting group, is then added sequentially to the growing chain. For example, as described in the Merrifield article, the protective group may be a carbobenzoxy group. By the procedure of coupling, deprotection, and coupling of the next amino acid, the desired amino acid sequence and chain length can be produced. As a final step, the protective group is removed from the N-terminal amino acid such as from the N-terminal arginine, and then is cleaved from the resin, using a suit¬ able reagent, such as trifluoroacetic acid and hy¬ drogen bromide. Since this synthesis procedure is well known, it is not believed that it will be necessary to further describe it herein. The pep¬ tide of this invention can be prepared by this syn¬ thesis procedure for use in reducing the fertility of mammals.

^TJRE OMPI To utilize the antigenic peptides of this invention (P-l to P-6) in the form of fertility re¬ ducing vaccines, the peptide used is conjugated to a carrier molecule, which is preferably a protein which itself elicits an antigenic response and which can be safely administered. For example, the selected peptide can be coupled to tetanus toxoid for administration by intramuscular injection. For example, a mixture of l^_Mole tetanus toxoid, 60χ - Mole antigenic peptide, and 18 millimoles 1-ethyl- 3-(3 dimethyl aminopropyl) carbodiimide hydrochlo- ride reacted in water (pH 6) for 12 hours at room temperature and 24 hours at 4°C. gives a product containing 3.5 moles of peptide/mole of tetanus tox- oid. Excess reactants can be removed by dialysis or gel filtration. See Pique et al, Immunochemis- try, 15=.._^55-60 (1978). Alternatively, the peptide may be coupled using bisdiazotized benzidine (Bassiri et al, Endocrinology, 90: 722 (1972) or glutaraldehyde.

For intramuscular injection, the coupled peptide may be suspended in a sterile isotonic _ saline solution, or other conventional vehicle, and, if desired, an adjuvant may be included. A preferr- ed use of such a vacine is for administration to human females. Antibodies will be formed, which will appear in the oviduct fluids and thereby achieve a significant reduction in fertility. For this purpose, the amount to be administered will range from about 1 to 10 milligrams (mg) of the antigenic peptide.

The peptide compounds of this invention and their method of preparation are further illus¬ trated by the following examples. EXAMPLE I

Preparation of Linear Peptide Arg-Met-Val-Ser-Gly-Gln-Thr- Ar -Leu-Asp-Leu-Leu-Gln-Arg

Synthesis of the above peptide (P-6) can be carried out employing solid phase techniques now well known in the art. In a preferred proce¬ dure amino. protected arginine, representing the -C00H terminal group of the above peptide, is coupled to a conventional solid phase peptide syn¬ thesis resin such as chloromethyl polystyrene cross-linked with 1 to 2% divinyl benzene. The amino protecting group is then selectively removed utilizing a suitable reagent whose nature will depend on the protecting group used. In the pre¬ ferred embodiment the t-butyloxycarbonyl (Boc) group is utilized for amino group protection and 40% trifluoroacetic acid in methylene chloride is the selective deprotecting agent. After deprotec ion, the arginine resin is treated with protected glutamine, preferably N-Boc- Gluta ine, and dicyclohexylcarbodiimide in a manner known per se as to form a peptide bond between the free amino group of the arginine residue and the carboxyl group of protected glutamine.

The cycle of deprotection and coupling with, amino acid derivatives and dicyclohexylcarboi- i ide is then repeated with the remaining amino acids in the sequence order of the above peptide. Some of the amino acids required side-chain block¬ ing groups besides the alphaamino protection. Such amino acids and the blocking groups are as follows: Met CMBzl) , Ser (oBzl) ,Arg (Tos) ,Asp (oBzl) , THR(oBzl)

Where oBzl is benzyl, Tos is guanidino-p-Toluene- sulfonyl and MBzl is methoxybenzyl. Completion of the synthesis provided the following peptide coupled to the styrenedivinylben- zene copolymer resin:

TFA-Arg(Tos)-Met(mBzl)-Val-Ser(oBzl)- Gly-Gln-Thr(oBzl)-Arg(Tos)-Leu-Asp (oBzl)-Leu-Leu-Gln-Arg(Tos)-resin

Decoupling of the peptide from the resin is accomplished by treatment with liquid hydrogen fluoride with concomittant cleavage of all pro¬ tecting groups to produce the desired peptide. Attachment of N-Boc-Arginine(Tos) to chloro ethyl resin was performed by the cesium salt method. A sample of chloromethyl resin (200 g.) containing 0.74 mmol chloride per gram is treated with the cesium salt of Boc-Arginine(Tos) resulting from the neutrallization of Boc-Arginine(Tos) with cesium carbonate. About 38.6 grams of Boc-Arginine (Tos) is dissolved in 80% methanol and 20% water and adjusted to pH 7.0 with about 29 grams of cesium carbonate. The resulting solution is dried on a rotary evaporator, then dried three more times after three additions of 100 milliliters of xylene. To the cesium salt of Boc-Arginine(Tos) was added 200 grams of chloromethyl resin as above and suffi¬ cient l-Methyl-2-Pyrrolidinone to make about 1.90 liters total volume. The resulting mixture is stirred at 55°C. for 48 hours. The resin was then

OMPI fr^{r ~} mpo washed extensively with methanol, then water, then again with methanol. The resin was air dried, then dried under vacuum. After cleavage of Arginine from the resin with HF, amino acid analysis gave one peak corresponding to 0.48 mmol/gm.

A sample of the resin just described C6.0g.) was submitted to the following synthesis schedule: (1) Wash with three 100 ml. portions of methylene chloride; (2) removal of the Boc group with 40% TFA in methylene chloride for a one minute wash and for a 20 minute reaction time; (3) wash with three 100 ml. portions of methylene chloride; (4) wash with two 100 ml. portions of isopropanol; (_.5) wash with three 100 ml. portions of methylene chloride; (6) a one minute wash and ten minutes neutrallization with 100 ml. portions of 10% triethyla ine in methylene chloride; (7) wash with three portions of 100 ml. of methylene chloride; (8) add 2.5 equivalents (7.2 mmol) of Boc amino acid and 2.5 equivalents (7.2 mmol) of dicyclohexylcarbodiimide in methylene chloride and shake for 2 hours; (9) wash with three 100 ml. portions of methylene chloride; (10) wash with two 100 ml. portions of isopropanol; (11) wash with three 100 ml. portions of methylene chloride. The above cycle was repeated for the following N- protected amino acids:

Boc-Gln Boc-Thr (oBzl)

Boc-Leu Boc-Gln Boc-Leu Boc-Gly

Boc-Asp (oBzl) Boc-Ser (oBzl)

Boc-Leu Boc-Val

Boc-Arg (Tos) Boc-Met (mBzl)

Boc-Arg (Tos)

OMPI The protected peptide resin was sub¬ mitted to deprotection to give,the TFA salt of the protected peptide resin. The dried resin (5.88g) was stirred in the presence of 6 ml. of anisole and 60 ml. of liquid HF at 0°C for 1 hour. The HF was removed by vacuum and the oily residue was washed with two 50 ml. portions of ethyl ether. The pep¬ tide was extracted from the resin by three 50 ml. portions of 1 molar acetic acid and the combined . filtrates were lyophilized to give 2.27 grams of crude peptide. This was purified by 250 transfers in a counter-current distribution apparatus. The solvent system for the above fractionation was butanol:acetic acid:water at 4:1:5 ratios. Somewhat purified fractions from the counter-current distribution apparatus were further purified by column chromatography on diethylamino- ethylcellulose with a linear gradient of 0.01 to 0.5 molar ammonium bicarbonate to give 250 mg. of pure peptide.

Amino acid analysis of the pure peptide after acid hydrolysis gave: ammonia 1.76, Arg 2.91, Asp 0.99, Thr 1.00, Ser 0.99, Glu 2.081, Gly 1.01, Val 1.081, Met 0.97, Leu 3.04. This peptide gave a single spot with a Rf of 0.62 on cellulose thin layer chro atography with a solvent system of buta¬ nol:pyridine:acetic acid: ater of 15:10:3:12, and an rF of 0.53 with these same solvents of 42:24:4:30.

EXAMPLE II

The respective shorter chain sequence compounds of the invention are prepared by the

- method of Example 1 starting with the respective C- erminal amino acids; leucine for the 9-sequence compounds P-l, aspartic acid for the 10-sequence compounds P-2, leucine for the 11-sequence and 12-sequence compounds P-3 and P-4, and glutamine for the 13-sequence compound P-5, ending all se¬ quences, as shown above, with the N-terminal arginine.

For example, the 9-sequence P-l compound is prepared as follows:

Preparation of Linear Peptide Arg-Met-Val-Ser-Gly-Gln-Thr-Arg-Leu

Synthesis of the above peptide can be carried out employing solid phase techniques now well known in the art. In a preferred procedure amino protected leucine, representing the -C00H terminal group of the above peptide, is coupled to a conventional solid phase peptide synthesis resin such as chloromethyl polystyrene cross-linked with 1 to 2% divinyl benzene. The amino protecting group is then selectively removed utilizing a suitable reagent whose nature will depend on the protecting group used. In the preferred embodiment the t-butyloxycarbonyl (Boc) group is utilized for amino group protection and 40% trifluoroacetic acid in methylene chloride is the selective deprotecting agent.

After deprotection, the leucine resin is treated with protected arginine, preferably N-Boc- N -Tosylarginine, and dicyclohexylcarbodiimide in a manner known per se as to form a peptide bond between the free amino group of the leucine residue

OMPI and the carboxyl group of protected arginine.

The cycle of deprotection and coupling with amino acid derivatives and dicyclohexylcar- bodiimide is then repeated with the remaining amino acids in the sequence order of the above peptide. Some of the amino acids required side-chain block¬ ing groups besides the alphaamino protection. Such amino acids and the blocking groups are as follows:

Met(MBzl) ,Ser(oBzl) ,Arg(Tos) ,Thr(oBzl)

Where oBzl is benzyl, Tos is guanidino- p-Toluenesulfonyl and MBzl is methoxybenzyl.

Completion of the synthesis provided the following peptide coupled to the styrenedivinyl- benzene copolymer resin:

TFA-Arg(Tos)-Met(mBzl)-Val-Ser

(oBzl)-Giy-Gln-Thr(oBzl)-Arg(Tos)- Leu-resin

Decoupling of the peptide from the resin is accomplished by treatment with liquid hydrogen fluoride with concomittant cleavage of all pro¬ tecting groups to produce the desired peptide.

Attachment of N-Boc-leucine to chloro¬ methyl resin was performed by the cesium salt method. A sample of chloromethyl resin (200 g.) containing 0.74 mmol chloride per gram is treated with the cesium salt of Boc-leucine resulting from the neutralization of Boc-leucine with cesium car¬ bonate. About 38.6 grams of Boc-leucine is dis¬ solved in 80% methanol and 20% water and adjusted to pH 7.0 with about 29 grams of cesium barbonate. The resulting solution is dried on a rotary eva-

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OMPI porator, then dried three more times after three additions of 100 milliliters of xylene. To the cesium salt of Boc-leucine was added 200 grams of chloromethyl resin as above and sufficient 1-Methyl- 2-Pyrrolidinone to make about 1.90 liters total volume. The resulting mixture is stirred at 55°C. for 48 hours. The resin was then washed extensive¬ ly with methanol, then water, then again with methanol. The resin was air dried, then dried under vacumn. After cleavage of leucine from the resin with HF, amino acid analysis gave one peak corre¬ sponding to 0.48 mmol/gm.

A sample of the resin just described (_6.0g.) was ^"submitted to the following synthesis schedule: l wash with three 100 ml. portions of methylene chloride;. C2) removal of the Boc group with 40% TFA in methylene chloride for a one minute wash and for a 20 minute reaction time; (3) wash with three 100 ml. portions of methylene chloride; (4) wash with two 100 ml. portions of isopropanol; (5) wash with three 100 ml. portions of methylene chloride; (6) a one minute wash and ten minutes neutrallization with 100 ml. portions of 10% tri- ethylamine in methylene chloride; (7) wash with three portions of 100 ml. of methylene chloride; (8) add 2.5 equivalents (7.2 mmol) of Boc amino acid and 2.5 equivalents (_.7.2 mmol) of dicyclohexyl- carbodiimide in methylene chloride and shake for 2 hours; C9) wash with three 100 ml. portions of methylene chloride; (10) wash with two 100 ml. portions of isopropanol; (11) wash with three 100 ml. portions of methylene chloride. The above cycle was repeated for the following N-protected amino acids: Boc-Arg(Tos)

Boc-Thr(oBzl)

Boc-Gln

Boc-Gly

Boc-SerCoBzl)

Boc-Val

Boc-Met( Bzl)

Boc-Arg(Tos)

The protected peptide resin was submitted to de- protection to give the TFA salt of the protected peptide resin. The dried resin (5.88g) was stirred in the presence of 6 ml. of anisole and 60 ml. of liquid HF at 0°C for 1 hour. The HF was removed by vacumn and the oily residue was washed with two 50 ml. portions of ethyl ether. The peptide was extracted from the resin by three 50 ml. portions of 1 molar acetic acid and the combined filtrates were lyophilized to give 2.27 grams of crude pep¬ tide. This was purified by 250 transfers in a counter-current distribution apparatus. The sol¬ vent system for the above fractionation was butanol:acetic acid;water at 4:1:5 ratios.

Somewhat purified fractions from the counter-current distribution apparatus were fur- ther purified by column chrom tography on diethyl- aminoethylcellulose with a linear gradient of 0.01 to 0.5 molar ammonium bicarbonate to give 250 mg. of pure peptide.

Claims

THE CLAIMSI claim:

1. The antigenic peptide compounds having chain lengths of from 9 to 14 amino acids arranged in a sequence from N-terminal to C- terminal amino acids which include the antigenic sequence Arg-Met-Val-Ser-Gly-Gln-Thr-Arg-Leu, said compounds being selected from the class of compounds consisting of:

(a) Arg-Met-Val-Ser-Gly-Gln-Thr-Arg-Leu,

Cb) Arg-Met-Val-Ser-Gly-Gln-Thr-Arg-Leu-Asp,

Cc) Arg-Met-Val-Ser-Gly-Gln-Thr-Arg-Leu-Asp-Leu^',

C ) Arg-Met-Val-Ser-Gly-Gln-Thr-Arg-Leu-Asp-Leu- Leu,

Ce) Arg-Met-Val-Ser-Gly-Gln-Thr-Arg-Leu-Asp-Leu- Leu-Gin, and f) Arg-Met-Val-Ser-Gly-Gln-Thr-Arg-Leu-Asp-Leu- Leu-Gin-Arg,

wherein Gly represents glycine, and Arg, Met, Val, Ser, Gin, Thr, Leu, Asp, respectively represent the L-amino acid forms of arginine, methionine, valine, serine, glutamine, threonine, leucine, and aspartic acid.

2. The antigenic peptide of claim 1 having the amino acid sequence (a) .

OMPI

3. The antigenic peptide of claim 1 having the amino acid sequence (b) .

4. The antigenic peptide of claim 1 having the amino acid sequence (c) .

5. The antigenic peptide of claim 1 having the amino acid sequence (d) .

6. The antigenic peptide of claim 1 having the amino acid sequence (e) .

7. The antigenic peptide of claim 1 having amino acid sequence (f) .