Peptides and methods for treatment of neurodegenerative diseases

Patent metadata

Field	Value
Publication number	US-10864244-B2
Application number	US-201816108605-A
Country	US
Kind code	B2
Filing date	Aug 22, 2018
Priority date	Feb 22, 2016
Publication date	Dec 15, 2020
Grant date	Dec 15, 2020

Abstract

The present disclosure provides pharmaceutical compositions comprising rationally designed peptide analogs of the p65-TAD binding region of GILZ to selectively sequester activated p65. Structural and functional analyses suggest that select GILZ analog (GA) bind p65-TAD with optimum affinity, exhibit an estimated half minimal lethal dose comparable to known peptide drugs and suppress Aβ1-42 induced cytotoxicity. Furthermore, the present disclosure provides uses and methods of using the pharmaceutical compositions, and uses and methods of using pharmaceutical formulations comprising the pharmaceutical compositions, for the treatment of neurodegenerative diseases such as Alzheimer's Disease, Parkinson's Disease, multiple sclerosis, and amyotrophic lateral sclerosis (ALS).

First claim

The invention claimed is:

1. A pharmaceutical composition comprising a polypeptide from 8 to 12 amino acid residues, the polypeptide comprising the sequence of XPXXP, wherein P is proline; and the first X is A or K, and the third X is Q, A, or S, wherein the polypeptide forms a PP II helical conformation and interacts with p65 residues F 534 and F 542 .

2. The pharmaceutical composition of claim 1 , wherein the polypeptide comprises the sequence of APKPYQPRG (SEQ ID NO: 29).

3. The pharmaceutical composition of claim 1 , wherein the polypeptide comprises the sequence of EPAPXXPXX (SEQ ID NO: 1),
and wherein the polypeptide comprises a sequence selected from the group consisting of EPAPLAPYG (SEQ ID NO: 13), EPAPYQPEG (SEQ ID NO: 24), EPAPESPQV (SEQ ID NO: 17), and EPAPEQPDG (SEQ ID NO: 18).

4. The pharmaceutical composition of claim 3 , wherein the polypeptide comprises the sequence of EPAPLAPYG (SEQ ID NO: 13).

5. The pharmaceutical composition of claim 3 , wherein the polypeptide comprises the sequence of EPAPYQPEG (SEQ ID NO: 24).

6. The pharmaceutical composition of claim 3 , wherein the polypeptide comprises the sequence of EPAPESPQV (SEQ ID NO: 17).

7. The pharmaceutical composition of claim 3 , wherein the polypeptide comprises the sequence of EPAPEQPDG (SEQ ID NO: 18).

8. The pharmaceutical composition of claim 1 , wherein the first X is A.

9. The pharmaceutical composition of claim 1 , wherein the first X is K.

10. The pharmaceutical composition of claim 1 , wherein the third X is Q.

11. The pharmaceutical composition of claim 1 , wherein the third X is S.

12. The pharmaceutical composition of claim 1 , wherein the first X is A, and the third X is Q, S, or A.

13. The pharmaceutical composition of claim 1 , wherein the first X is A, and the third X is Q.

14. The pharmaceutical composition of claim 1 , wherein the first X is A, and the third X is S.

15. The pharmaceutical composition of claim 1 , wherein the first X is A, and the third X is A.

16. The pharmaceutical composition of claim 1 , wherein the first X is K, and the third X is Q.

17. A pharmaceutical composition comprising a polypeptide from 8 to 12 amino acid residues, the polypeptide comprising a tetrapeptide having the sequence of PXXP, wherein P is proline; and the second X is Q or S, wherein the polypeptide forms a PP II helical conformation and interacts with p65 residues F 534 and F 542 .

18. The pharmaceutical composition of claim 17 , wherein the second X is Q.

19. The pharmaceutical composition of claim 17 , wherein second X is S.

Assignees

• Univ Indiana Res & Tech Corp

Inventors

• Srinivasan Mythily
• Lahiri Debomoy

Classifications

• C07K14/81

  Protease inhibitors · CPC title

• C07K14/4746

  p53 · CPC title

• C07K14/4703

  Inhibitors; Suppressors · CPC title

• C07K14/4702

  Regulators; Modulating activity · CPC title

• C07K14/47

  from mammals · CPC title