Cyclic polypeptides, method for obtaining them and the therapeutic use thereof
The invention relates to a polypeptide #including the following amino acid sequence: W-S-X1-W-X2-X3-C-S-X4-C-G (SEQ ID NO: 59), wherein X1, X2 and X3 are, independently of one another, S or G, X4 is R-S or V-S or V-T or R-T, and both cysteines form a disulfide bridge.
1. Polypeptide comprising the amino acid sequence SEQ ID NO: 59,
wherein the two cysteines form a disulfide bridge; and
wherein the polypeptide is substantially free of the reduced or dimeric or oligomeric forms of the polypeptide as well as derivatives of the polypeptide in which the thiol groups are in the sulfoxide or sulfone form.
2. Polypeptide according to claim 1 wherein the amino acid sequence comprises SEQ ID NO: 1.
3. Polypeptide according to claim 1 wherein the amino acid sequence comprises SEQ ID NO: 2.
4. A pharmaceutical composition of comprising as active ingredient a polypeptide according to claim 3 and one or more pharmaceutically-acceptable excipients.
5. The pharmaceutical composition of claim 4 further comprising a second polypeptide comprising the amino acid sequence SEQ ID NO: 59
wherein the two cysteines form a disulfide bridge; and
wherein the second polypeptide is substantially free of the reduced or dimeric or oligomeric forms of the second polypeptide as well as derivatives of the second polypeptide in which the thiol groups are in the sulfoxide or sulfone form.
6. Polypeptide according to claim 1 wherein the polypeptide consists of the amino acid sequence SEQ ID NO: 69.
7. Polypeptide according to claim 1 wherein the polypeptide consists of the amino acid sequence SEQ ID NO: 2.
8. Polypeptide according to claim 7 ,
wherein the polypeptide has a purity greater than 80%.
9. Polypeptide according to claim 1 wherein the polypeptide consists of the amino acid sequence SEQ ID NO: 59 and
wherein the polypeptide has a purity greater than 80%.
10. Pharmaceutical composition comprising as active ingredient a polypeptide according to claim 1 and one or more pharmaceutically-acceptable excipients.
11. Method for obtaining the polypeptide of amino acid sequence SEQ ID NO: 59
having the two cysteines form a disulfide bridge, from a starting polypeptide of sequence SEQ ID NO: 70,
wherein the starting polypeptide of sequence SEQ ID NO: 70 is in solution;
comprising forming a disulfide bridge in the presence of albumin in the starting polypeptide of sequence SEQ ID NO: 70.
12. Method according to claim 11 wherein albumin and the starting polypeptide are present in a molar:molar ratio of 1:1 to 1:100.
13. The method of claim 12 , wherein said molar:molar ratio is 1:1 to 1:10.
14. The method of claim 12 , wherein said molar:molar ratio is 1:1.
15. Method according to claim 11 wherein the forming a disulfide bridge in the presence of albumin in the starting polypeptide is carried out in ambient air.
16. The method according to claim 11 , wherein the forming a disulfide bridge in the presence of albumin in the starting polypeptide is carried out without detaching the starting polypeptide from the resin used for the peptide synthesis of these polypeptides, and wherein the polypeptide of sequence SEQ ID NO: 59 is then obtained by separating the polypeptide from the resin after the disulfide bond formation.
17. Method for obtaining the polypeptide of amino acid sequence SEQ ID NO: 2
from a starting polypeptide of sequence SEQ ID NO: 58:
comprising forming a disulfide bridge in the presence of albumin in the starting polypeptide of sequence SEQ ID NO: 58.
18. Method according to claim 17 , wherein albumin and the starting polypeptide are present in a molar:molar ratio of 1:1 to 1:100.
19. The method of claim 18 , wherein said molar:molar ratio is 1:1 to 1:10.
20. The method of claim 18 , wherein said molar:molar ratio is 1:1.
21. The method according to claim 17 , wherein the forming a disulfide bridge in the presence of albumin in the starting polypeptide is carried out in ambient air.
22. The method according to claim 17 , wherein the forming a disulfide bridge in the presence of albumin in the starting polypeptide is carried out without detaching the starting polypeptide from the resin used for the peptide synthesis of the polypeptide, and wherein the polypeptide of sequence SEQ ID NO: 2 is then obtained by separating the polypeptide from the resin after the disulfide bond formation.