Compositions comprising bowman-birk protease inhibitors and variants thereof
The present invention provides compositions and methods related to expression of protease inhibitors and variants thereof in bacterial species. The present invention further provides fusion nucleic acids, vectors, fusion polypeptides, and processes for obtaining the protease inhibitors.
1. A composition comprising a fusion protein, wherein said fusion protein comprises a Bowman Birk Inhibitor (BBI) comprising SEQ ID NO:13, wherein the trypsin and/or chymotrypsin loop of said SEQ ID NO: 13 is replaced with a vascular endothelial growth factor binding peptide consisting of SEQ ID NO: 9.
2. The composition of claim 1 , wherein the trypsin and chymotrypsin loop of said SEQ ID NO: 13 is replaced with a VEGF binding peptide consisting of SEQ ID NO: 9.
3. A protease inhibitor composition comprising a Bowman Birk Inhibitor (BBI) comprising SEQ ID NO:13, wherein the trypsin or chymotrypsin loop of said SEQ ID NO: 13 is replaced with the amino acid sequence of SEQ ID NO:9.
4. The composition of claim 1 , wherein said fusion protein binds a vascular endothelial growth factor.
5. The composition of claim 1 , wherein said fusion protein further comprises at least one catalytic domain and a cleavage site, wherein said catalytic domain is selected from the group consisting of cellulase, cutinase, and disulfide isomerase.
6. The composition of claim 1 , wherein said fusion protein further comprises at least one linker sequence.
7. The composition of claim 6 , wherein said, wherein said linker sequence is selected from the group consisting of SEQ ID NOS:141-143.
8. A composition comprising a fusion protein, wherein said fusion protein comprises a Bowman Birk Inhibitor (BBI) comprising SEQ ID NO:13, wherein the trypsin and/or chymotrypsin loop of said SEQ ID NO: 13 is replaced with a vascular endothelial growth factor binding peptide consisting of SEQ ID NO: 9, and wherein said SEQ ID NO: 13 is truncated at the N- and/or C-terminus, with as many as seven N-terminal residues up to the first cysteine (Cys8) and/or as many as nine C-terminal residues up to the last cysteine (Cys62) removed.