Polypeptides targeting vascular endothelial growth factor receptor-2 and αvβ3 integrin
Polypeptides comprising variant vascular endothelial growth factor sequences are provided. The polypeptides are useful in cancer imaging, cancer diagnosis, monitoring and treatment as well as treatment of diseases characterized by excessive neovascularization.
1. A human vascular endothelial growth factor (VEGF) variant polypeptide, comprising:
a first human VEGF polypeptide comprising F17A and E64A substitutions, and linked through a polypeptide linker to a second human VEGF polypeptide comprising I46A mutation,
wherein said second human VEGF polypeptide comprises an integrin-recognition RGD motif containing loop selected from the sequences set forth in any one of SEQ ID NO:29-SEQ ID NO:75 and replacing a loop 3 sequence of said VEGF polypeptide to provide a single-chain VEGF antagonist,
whereby the VEGF variant exhibits a high affinity to VEGF receptor-2 (VEGFR2) and alpha v beta 3 integrin.
2. The VEGF variant of claim 1 , wherein said loop 3 sequence is I83-Q89.
3. A VEGF variant, having an amino acid sequence set forth in any one of SEQ ID NO:5-8, and SEQ ID NO:19-27.
4. A VEGF variant, having an amino acid sequence set forth in SEQ ID NO:9-18 and 19-27, further comprising the modification of replacing amino acid residues of loop 3 in one of said human VEGF with an RGD motif.
5. A single-chain antagonistic human VEGF variant having an amino acid sequence set forth in SEQ ID NO:9-18.
6. A VEGF variant according to any one of claims 1 , 4 or 5 , further comprising a functional conjugate.
7. The VEGF variant according to claim 6 , wherein said functional conjugate is a detectable moiety.
8. A pharmaceutical composition comprising a VEGF variant according to any one of claims 1 , 4 or 5 , and a pharmaceutically acceptable excipient.
9. An isolated nucleic acid encoding a VEGF variant according to claim 5 .
10. A human vascular endothelial growth factor (VEGF) variant polypeptide, comprising:
a first human VEGF polypeptide linked through a polypeptide linker to a second human VEGF polypeptide:
wherein said first human VEGF polypeptide comprises F17A and E64A amino acid substitutions;
wherein said second human VEGF polypeptide comprises I46A and I83A amino acid substitutions, and an integrin-recognition RGD motif containing loop having the sequence set forth in SEQ ID NO:69,
to provide a single-chain VEGF antagonist that exhibits a high affinity to VEGF receptor-2 (VEGFR2) and alpha v beta 3 integrin.
11. A method of inhibiting VEGF-mediated proliferation or migration of endothelial cells, the method comprising contacting an endothelial cell with a VEGF variant according to claim 5 .
12. The method of claim 11 wherein said contacting is performed in vivo.