IP Library Granted Patent US 8,426,367
Granted Patent B2
US 8,426,367 · App. 12/530,137 · Granted Apr 23, 2013

Peptides specific for human blood outgrowth endothelial cells

Inventors: Cam Patterson (Chapel Hill, NC); Anka Veleva (Cary, NC); Stuart Cooper (Powell, OH)
Assignees: The University of North Carolina at Chapel Hill; North Carolina State University; The Ohio State University Research Foundation
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Quick Facts
Patent No.
US 8,426,367
App. No.
12/530,137
Granted
Apr 23, 2013
Kind
B2
Abstract

Provided herein are compositions and methods for binding outgrowth endothelial cells (OEC). The compositions consist of peptide ligands capable of binding OEC with high affinity and specificity. The compositions of the invention include peptides set forth in SEQ ID NO: 1-38 and variants and derivatives thereof. Compositions also include the nucleotide sequences encoding the peptides of the invention. The compositions find use in methods for the isolation of OEC and for the recruitment and retention of OEC to sites of therapeutic interest. Methods for the identification and isolation of other peptides capable of binding OEC are also provided.

Claims (30)

1. An isolated peptide that binds outgrowth endothelial cells (OEC) wherein said peptide comprises the amino acid sequence of SEQ ID NO:26 or a variant thereof, wherein said variant differs from SEQ ID NO:26 by one amino acid and wherein said variant binds OEC.

2. The peptide of claim 1 , wherein said peptide has from about 11 to about 30 amino acids.

3. The peptide of claim 1 , wherein said peptide contains at least one motif selected from the group consisting of PPR, TP, and PPS.

4. A method for sequestering and retaining outgrowth endothelial cells (OEC) at a therapeutic site of interest, said method comprising introducing at said therapeutic site at least one peptide wherein said peptide comprises the amino acid sequence of SEQ ID NO:26 or a variant thereof, wherein said variant differs from SEQ ID NO:26 by one amino acid and wherein said variant binds OEC.

5. The method of claim 4 , wherein said peptide has from about 11 to about 30 amino acids.

6. The method of claim 4 , wherein said peptide contains at least one motif selected from the group consisting of PPR, TP, and PPS.

7. The method of claim 4 , wherein said peptide is bound to an outgrowth endothelial cell.

8. The method of claim 4 , wherein said therapeutic site of interest is selected from the group consisting of an area where angiogenesis is desired, an area of ischemic injury, an area of organ transplantation, and an area of vascular injury.

9. A kit comprising at least one of the peptides of claim 1 .

10. A composition comprising at least one peptide for use in a method for sequestering and retaining outgrowth endothelial cells (OEC) at a therapeutic site of interest, said method comprising introducing at said therapeutic site at least one peptide, wherein said peptide comprises the amino acid sequence of SEQ ID NO:26 or a variant thereof, wherein said variant differs from SEQ ID NO:26 by one amino acid and wherein said variant binds OEC.

11. The method composition of claim 10 , wherein said peptide is bound to an OEC.

12. The composition of claim 10 , wherein said therapeutic site of interest is selected from the group consisting of an area where angiogenesis is desired, an area of ischemic injury, an area of organ transplantation, and an area of vascular injury.

13. The peptide of claim 1 , wherein said peptide is attached to an implant.

14. The peptide of claim 13 , wherein said peptide is bound to an OEC.

15. An implant coated with at least one peptide, wherein said peptide comprises the amino acid sequence of SEQ ID NO:26 or a variant thereof, wherein said variant differs from SEQ ID NO:26 by one amino acid and wherein said variant binds outgrowth endothelial cells (OEC).

16. The implant of claim 15 , wherein said peptide contains at least one motif selected from the group consisting of PPR, TP, and PPS.

17. The implant of claim 15 , wherein said implant further comprises OEC bound to said peptide.

18. The implant of claim 15 , wherein said peptide binds at least 10% more to OEC than a different cell type.

19. The implant of claim 15 , wherein said peptide binds at least 50% more to OEC than a different cell type.

20. The implant of claim 15 , wherein said peptide has from about 11 to about 30 amino acids.

21. The peptide of claim 1 , wherein said peptide binds at least 10% more to OEC than a different cell type.

22. The peptide of claim 1 , wherein said peptide binds at least 50% more to OEC than a different cell type.

23. The method of claim 4 , wherein said peptide binds at least 10% more to OEC than a different cell type.

24. The method of claim 4 , wherein said peptide binds at least 50% more to OEC than a different cell type.

25. The method of claim 4 , wherein said peptide is attached to an implant.

26. The composition of claim 10 , wherein said peptide binds at least 10% more to OEC than a different cell type.

27. The composition of claim 10 , wherein said peptide binds at least 50% more to OEC than a different cell type.

28. The composition of claim 10 , wherein said peptide has from about 11 to about 30 amino acids.

29. The composition of claim 10 , wherein said peptide contains at least one motif selected from the group consisting of PPR, TP, and PPS.

30. A pharmaceutical composition comprising at least one peptide according to claim 1 and a pharmaceutically acceptable carrier.

Assignments (1)
CONFIRMATORY LICENSE Recorded May 11, 2012
From: THE UNIVERSITY OF NORTH CAROLINA AT CHAPEL HILL
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 028193/0132 →
Continuity (2)
Provisional Application 60892987 · Mar 5, 2007
Related Publication 20100190703A1 · Jul 29, 2010