IP Library Granted Patent US 7,638,598
Granted Patent B2
US 7,638,598 · App. 10/119,288 · Granted Dec 29, 2009

ErbB interface peptidomimetics and methods of use thereof

Assignee: The Trustees Of The University Of Pennsylvania
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Quick Facts
Patent No.
US 7,638,598
App. No.
10/119,288
Granted
Dec 29, 2009
Kind
B2
Abstract

Peptides, mimetics and antibodies of erbB, TNF, and IgSF receptors and pharmaceutical compositions comprising the same are described. Methods of using such antibodies, peptides, and mimetics in therapeutic, prophylactic, imaging and diagnostic applications are disclosed.

Claims (30)

1. An isolated peptide having the formula:

R 1 -R 2 -R 3 -R 4 -R 5 -R 6 -R 7

wherein:

R 1 is 1-6 amino acid residues, at least one of which is tyrosine or phenylalanine;

R 2 is cysteine or penicillamine;

R 3 is a bond;

R 4 is 7-8 amino acids;

R 5 is a bond;

R 6 is cysteine or penicillamine;

R 7 is 1-5 amino acid residues, at least one of which is tyrosine or phenylalanine;

wherein: R 1 , R 2 , R 3 , R 4 , R 5 , R 6 and R 7 , taken together, are 30 amino acids or less;

R 1 is selected from the group consisting of F; S-Y; G-S-Y; Y; G-G-S-Y (SEQ ID NO:21); and G-G-G-S-Y (SEQ ID NO:22);

R 2 and R 6 are connected by a bond to cyclicize said peptide;

R 4 is selected from the group consisting of F-P-D-E-E-G-A (SEQ ID NO: 1); and F-Y-P-D-E-E-G-A (SEQ ID NO:2); and

R 7 is selected from the group consisting of F; Y-G-G-S (SEQ ID NO:27); Y-G-G-G (SEQ ID NO:23); Y-G-G-G-S (SEQ ID NO:24); Y; Y-G, and Y-G-G.

2. The peptide of claim 1 wherein R 1 comprises S-Y, G-S-Y, F or Y.

3. The peptide of claim 1 wherein R 1 consists of S-Y, G-S-Y, F or Y.

4. The peptide of claim 1 wherein R 2 is cysteine, R 6 is cysteine and R 1 comprises S-Y.

5. The peptide of claim 1 wherein R 1 comprises S-Y.

6. The peptide of claim 1 wherein R 4 is SEQ ID NO: 1.

7. The peptide of claim 1 wherein R 4 is SEQ ID NO: 2.

8. The peptide of claim 1 wherein R 7 is selected from the group consisting of Y, Y-G, and Y-G-G.

9. The peptide of claim 1 wherein R 1 comprises F or Y.

10. The peptide of claim 1 wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 and R 7 , taken together, are less than 20 amino acids.

11. The peptide of claim 1 wherein said peptide has an amino acid sequence selected from the group consisting of SEQ ID NOs: 4-20, 25, and 26.

12. The peptide of claim 1 wherein said peptide comprises an amino acid sequence of SEQ ID NO:21.

13. A conjugated composition comprising a peptide according to claim 1 linked to one or more detectable agent, cytotoxic agent or chemotherapeutic agent.

14. The conjugated composition of claim 13 wherein said peptide is linked to a detectable agent, said detectable agent being a radioisotope.

15. The conjugated composition of claim 13 wherein said peptide is linked to a cytotoxic agent selected from the group consisting of cytotoxic drugs, toxins and cytostatic drugs.

16. A pharmaceutical composition comprising a peptide according to claim 1 , and a pharmaceutically acceptable carrier or diluent.

Assignments (3)
CONFIRMATORY LICENSE Recorded Nov 27, 2022
From: UNIVERSITY OF PENNSYLVANIA
To: NIH - DEITR
Reel/Frame 061883/0730 →
CONFIRMATORY LICENSE Recorded Nov 8, 2022
From: UNIVERSITY OF PENNSYLVANIA
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 061896/0979 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 15, 2002
From: GREENE, MARK I.; MURALI, RAMACHANDRAN; ZHANG, HONGTAO; RICHTER, MARK; BEREZOV, ALAN; LIU, QINGDU; CHEN, JINQIU
To: TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA, THE
Reel/Frame 013207/0882 →
Continuity (3)
Provisional Application 6028203700 · Apr 6, 2001
Provisional Application 6030986400 · Aug 3, 2001
Related Publication 20090286737A1 · Nov 19, 2009