IP Library Granted Patent US 8,697,651
Granted Patent B2
US 8,697,651 · App. 13/328,315 · Granted Apr 15, 2014

Amyloid β fibrillogenesis-inhibiting peptide

Inventor: Kazuhisa Sugimura (Kogoshima, JP)
Assignee: Kagoshima University
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Quick Facts
Patent No.
US 8,697,651
App. No.
13/328,315
Granted
Apr 15, 2014
Kind
B2
Abstract

The present invention provides a peptide which functions as a mimic peptide of an amyloid β peptide and is capable of inhibiting the fibrillogenesis of an amyloid β peptide. The present invention relates to an 8- to 30-amino acid residue peptide comprising an amino acid sequence represented by the following formula (I): X 1 -Asp-X 2 -X 3 -X 4 -Pro-X 5 -X 6 (SEQ ID NO: 28) (I), wherein X 1 represents a branched chain amino acid, and X 2 , X 3 , X 4 , X 5 , and X 6 are the same or different and each represents an α-amino acid, and to a pharmaceutical composition and an amyloid β fibrillogenesis inhibitor comprising the peptide.

Claims (21)

1. A 12- to 30-amino acid residue peptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12, SEQ ID NO: 13, SEQ ID NO: 14, and SEQ ID NO: 15.

2. The peptide according to claim 1 , wherein the peptide is a 23- to 30-amino acid residue peptide comprising a TAT sequence represented by the following formula:

(SEQ ID NO: 30)

Tyr-Gly-Arg-Lys-Lys-Arg-Arg-Gln-Arg-Arg-Arg.

3. A composition comprising the peptide according to claim 1 and a carrier or excipient.

4. The peptide according to claim 1 , wherein the peptide comprises the amino acid sequence of SEQ ID NO: 9.

5. The peptide according to claim 1 , wherein the peptide comprises the amino acid sequence of SEQ ID NO: 10.

6. The peptide according to claim 1 , wherein the peptide comprises the amino acid sequence of SEQ ID NO: 11.

7. The peptide according to claim 1 , wherein the peptide comprises the amino acid sequence of SEQ ID NO: 12.

8. The peptide according to claim 1 , wherein the peptide comprises the amino acid sequence of SEQ ID NO: 13.

9. The peptide according to claim 1 , wherein the peptide comprises the amino acid sequence of SEQ ID NO: 14.

10. The peptide according to claim 1 , wherein the peptide comprises the amino acid sequence of SEQ ID NO: 15.

11. The peptide according to claim 2 , wherein the peptide comprises the amino acid sequence of SEQ ID NO: 9.

12. The peptide according to claim 2 , wherein the peptide comprises the amino acid sequence of SEQ ID NO: 10.

13. The peptide according to claim 2 , wherein the peptide comprises the amino acid sequence of SEQ ID NO: 11.

14. The peptide according to claim 2 , wherein the peptide comprises the amino acid sequence of SEQ ID NO: 12.

15. The peptide according to claim 2 , wherein the peptide comprises the amino acid sequence of SEQ ID NO: 13.

16. The peptide according to claim 2 , wherein the peptide comprises the amino acid sequence of SEQ ID NO: 14.

17. The peptide according to claim 2 , wherein the peptide comprises the amino acid sequence of SEQ ID NO: 15.

18. A peptide selected from the group consisting of SEQ ID No: 24 and SEQ ID No: 25.

19. A method for inhibiting amyloid β 1-42 fibrillogenesis comprising administering an effective amount of the peptide according to claim 18 to a subject in need thereof.

Priority Claims (1)
JP 2006-125769 · Apr 28, 2006 · national
Continuity (2)
Division 12298672
Related Publication 20120190626A1 · Jul 26, 2012