CVN-12p1: a recombinant allosteric lectin antagonist of HIV-1 envelope gp120 interactions
View Patent ↗The invention provides a recombinant multi-functional chimera of CVN and 12p1. Chimeras of CVN and 12p1 present a model for targeting gp120 at two discrete sites, by two different modes of inhibition and with increasing potency versus either component alone. A chimera of the invention combines the high affinity suppression of viral activity by CVN with the allosteric suppression of viral envelope binding to both CD4 and co-receptor by 12p1.
1. A chimeric protein comprising a first amino acid sequence of cyanovirin, a second amino acid sequence of 12p1 and a linker covalently connecting the first amino acid sequence with the second amino acid sequence, wherein the first amino acid sequence is selected from the group consisting of SEQ ID NO: 2 and SEQ ID NO: 4, and the second amino acid sequence is selected from the group consisting of SEQ ID NO: 12 and SEQ ID NO: 13, and wherein the linker has one through seven penta-peptide repeats of glycine and serine.
2. The chimeric protein of claim 1 , wherein the linker comprises a sequence encoded by SEQ ID NO: 8.
3. The chimeric protein of claim 2 , wherein the linker has at least three repeats of the sequence encoded by SEQ ID NO: 8.
4. The chimeric protein of claim 2 , wherein the linker has at least five repeats of the sequence encoded by SEQ ID NO:8.
5. The chimeric protein of claim 1 encoded by SEQ ID NO: 10.
6. The chimeric protein of claim 1 encoded by SEQ ID NO: 15.
7. The chimeric protein of claim 3 , wherein the linker is a sequence encoded by SEQ ID NO: 9.
8. A pharmaceutical composition comprising the chimeric protein of claim 1 and a pharmaceutically acceptable carrier.
9. A pharmaceutical composition comprising:
(i) an isolated and purified protein of cyanovirin having an amino acid sequence selected from the group consisting of SEQ ID NO: 2 and SEQ ID NO: 4; and
(ii) an isolated and purified peptide having an amino acid sequence selected from the group consisting of SEQ ID NO: 12 and SEQ ID NO: 13.
10. A method of inhibiting HIV in a mammal comprising contacting a cell of the mammal with the pharmaceutical composition of claim 9 in an amount effective to block HIV binding to the cell.
11. A method of inhibiting HIV in a mammal comprising contacting a cell of the mammal with the pharmaceutical composition of claim 8 in an amount effective to block HIV binding to the cell.