IP Library › Granted Patent US 8,198,405
Granted Patent B2
US 8,198,405 · App. 12/182,673 · Granted Jun 12, 2012

Stabilized alpha helical peptides and uses thereof

Assignees: Dana-Farber Cancer Institute, Inc.; President and Fellows of Harvard College
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Quick Facts
Patent No.
US 8,198,405
App. No.
12/182,673
Granted
Jun 12, 2012
Kind
B2
Abstract

Novel polypeptides and methods of making and using the same are described herein. The polypeptides include cross-linking (“hydrocarbon stapling”) moieties to provide a tether between two amino acid moieties, which constrains the secondary structure of the polypeptide. The polypeptides described herein can be used to treat diseases characterized by excessive or inadequate cellular death.

Claims (31)

1. A cross-linked polypeptide comprising an amino acid sequence which is at least 60% identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 92-111, wherein the polypeptide comprises a crosslinker connecting a first amino acid to a second amino acid, and wherein the first and second amino acids are separated by 3 or 6 amino acids.

2. A cross-linked polypeptide comprising an amino acid sequence which is at least 80% identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 92-111 and wherein the cross-linked polypeptide comprises up to 50 amino acids.

3. The cross-linked polypeptide of claim 2 , wherein the cross-linked polypeptide comprises an amino acid sequence that is at least 90% identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 92-111 and wherein the cross-linked polypeptide comprises up to 50 amino acids.

4. The cross-linked polypeptide of claim 2 , wherein the cross-linked polypeptide comprises an amino acid sequence that is at least 80% identical to SEQ ID NO: 111 and wherein the cross-linked polypeptide comprises up to 50 amino acids.

5. The cross-linked polypeptide of claim 3 , wherein the cross-linked polypeptide comprises an amino acid sequence that is at least 90% identical to SEQ ID NO: 111 and wherein the cross-linked polypeptide comprises up to 50 amino acids.

6. The cross-linked polypeptide of claim 5 , wherein the cross-linked polypeptide comprises SEQ ID NO: 111.

7. The cross-linked polypeptide of claim 6 , wherein the amino acid sequence of the cross-linked polypeptide is IWIAQELR*IGD*FNAYYARR (SEQ ID NO:111) and wherein * is a tethered amino acid.

8. The cross-linked polypeptide of claim 7 , wherein an alpha carbon of the tethered amino acid is in an S configuration.

9. The cross-linked polypeptide of claim 8 , wherein a tether connecting the alpha carbons of the tethered amino acids contains nine consecutive C—C bonds.

10. The cross-linked polypeptide of claim 1 , wherein the polypeptide has the Formula:

wherein;

each R 1 and R 2 are independently H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroarylalkyl, or heterocyclylalkyl;

R 3 is a crosslinker which is alkyl, alkenyl, alkynyl; [R 4 —K—R 4 ] n or a naturally occurring amino acid side chain; each of which is substituted with 0-6 R 5 ;

R 4 is alkyl, alkenyl, or alkynyl;

R 5 is halo, alkyl, OR 6 , N(R 6 ) 2 , SR 6 , SOR 6 , SO 2 R 6 , CO 2 R 6 , R 6 , a fluorescent moiety, or a radioisotope;

K is O, S, SO, SO 2 , CO, CO 2 , CONR 6 , or

R 6 is H, alkyl, or a therapeutic agent;

n is an integer from 1-4;

x is 3 or 6;

each y is independently an integer from 1-100;

z is an integer from 1-10; and

each Xaa is independently an amino acid.

11. The cross-linked polypeptide of claim 10 , wherein the polypeptide has a substantially alpha helical secondary structure in aqueous solution.

12. The cross-linked polypeptide of claim 1 , comprising an amino acid sequence which is at least 70% identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 92-111.

13. The cross-linked polypeptide of claim 1 , comprising an amino acid sequence which is at least 80% identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 92-111.

14. The cross-linked polypeptide of claim 1 , comprising an amino acid sequence which is at least 90% identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 92-111.

15. The cross-linked polypeptide of claim 1 , wherein the cross-linked polypeptide comprises up to 50 amino acids.

16. The cross-linked polypeptide of claim 2 , 3 , 4 , or 5 , wherein the cross-linked polypeptide comprises a crosslinker connecting a first amino acid to a second amino acid.

17. The cross-linked polypeptide of claim 16 , wherein the first and second amino acids are separated by 3 or 6 amino acids.

18. The cross-linked polypeptide of claim 16 , wherein the crosslinker is a hydrocarbon crosslinker.

19. The cross-linked polypeptide of claim 1 , 2 , 3 , 4 , or 5 , wherein the polypeptide has a substantially alpha-helical secondary structure in aqueous solution.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 11, 2008
From: WALENSKY, LOREN D.
To: DANA-FARBER CANCER INSTITUTE, INC.
Reel/Frame 021368/0536 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 11, 2008
From: HOWARD HUGHES MEDICAL INSTITUTE
To: DANA-FARBER CANCER INSTITUTE, INC.
Reel/Frame 021368/0597 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 11, 2008
From: VERDINE, GREGORY
To: PRESIDENT AND FELLOWS OF HARVARD COLLEGE
Reel/Frame 021368/0618 →
Continuity (4)
Continuation 10981873 · Nov 5, 2004
Provisional Application 60517848 · Nov 5, 2003
Provisional Application 60591548 · Jul 27, 2004
Related Publication 20090176964A1 · Jul 9, 2009