IP Library Granted Patent US 9,873,718
Granted Patent B2
US 9,873,718 · App. 14/889,604 · Granted Jan 23, 2018

Structure-based peptide inhibitors of P53 aggregation as a new approach to cancer therapeutics

Inventors: David S. Eisenberg (Los Angeles, CA); Alice Soragni (Los Angeles, CA); Lin Jiang (Los Angeles, CA)
Assignee: The Regents of the University of California
C07K7/06C07K14/4711C07K14/4746G06F19/16G06F19/18A61K38/00C07K2319/10C07K2319/33C07K2319/70
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Quick Facts
Patent No.
US 9,873,718
App. No.
14/889,604
Granted
Jan 23, 2018
Kind
B2
Abstract

This invention relates, e.g., to an inhibitory peptide or CPP inhibitor which specifically binds to p53 having an aberrant conformation (e.g., is aggregated or misfolded) and inhibits p53 amyloidogenic aggregation or restores proper folding of the misfolded protein. Methods of using the inhibitory peptide or CPP inhibitor (e.g. to treat subjects having tumors that comprise aggregated p53) are described.

Claims (20)

1. A cell penetrating peptide (CPP) inhibitor represented by the sequence (R 2-16 ) P I (L/Y/E/W) T (R/K) I T (L) E (SEQ ID NO: 19), provided the sequence does not comprise YTRITLE (SEQ ID NO: 5).

2. A pharmaceutical composition comprising the peptide of claim 1 and a pharmaceutically acceptable carrier.

3. A kit comprising the peptide of claim 1 , packaged in a container.

4. A method of making the peptide of claim 1 , comprising synthesizing it chemically or producing it recombinantly.

5. A peptide which comprises the amino acid sequence LTRITLE (SEQ ID NO: 4), wherein said amino acid sequence is coupled to 2 to 16 arginine (R) residues.

6. A pharmaceutical composition comprising the peptide of claim 5 and a pharmaceutically acceptable carrier.

7. A pharmaceutical composition comprising the peptide of claim 5 and a pharmaceutically acceptable carrier, wherein the peptide has been isolated.

8. A composition of matter comprising the peptide of claim 5 ;

wherein:

the peptide is coupled to 4 to 16 arginine residues.

9. The composition of claim 8 , wherein the peptide is coupled to the arginine residues by a peptide linker comprising 1-7 amino acids.

10. The composition of claim 8 , wherein the peptide forms a polycationic structure.

11. The composition of claim 8 , wherein the peptide forms an amphipathic structure.

12. The composition of claim 8 , wherein the peptide is less than 30 amino acids in length.

13. A composition of matter comprising:

the peptide of claim 5 ; and

a pharmaceutically acceptable carrier including a peptide stabilizing excipient.

14. The composition of claim 13 , wherein the peptide stabilizing excipient is a preservative that inhibits the growth of microorganisms.

15. A composition of matter comprising a peptide comprising the sequence RRRRRRRRRRPILTRITLE (SEQ ID NO: 22).

16. The CPP inhibitor of claim 1 represented by the sequence (R 2-16 ) P I L T R I T L E (SEQ ID NO: 19).

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 6, 2018
From: EISENBERG, DAVID S.; SORAGNI, ALICE; JIANG, LIN
To: THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
Reel/Frame 047426/0260 →
CONFIRMATORY LICENSE Recorded May 12, 2016
From: UNIVERSITY OF CALIFORNIA, LOS ANGELES
To: NATIONAL SCIENCE FOUNDATION
Reel/Frame 038688/0457 →
Continuity (2)
Provisional Application 61821157 · May 8, 2013
Related Publication 20160068569A1 · Mar 10, 2016