Protease resistant mutants of stromal cell derived factor-1 in the repair of tissue damage
View Patent ↗The present invention is directed stromal cell derived factor-1 peptides that have been mutated to make them resistant to digestion by the proteases dipeptidyl peptidase IV (DPPIV) and matrix metalloproteinase-2 (MMP-2) but which maintain the ability of native SDF-1 to attract T cells. The mutants may be attached to membranes formed by self-assembling peptides and then implanted at sites of tissue damage to help promote repair.
1. An isolated mutant form of stromal cell derived factor-1 (SDF-1) peptide comprising a mutant SDF-1 (mSDF-1) or X p -mSDF-1, wherein:
a) X is proteinogenic amino acid(s) or a protease protective organic group;
b) p is any integer from 1 to 4;
c) said mSDF-1 comprises the amino acid sequence of SEQ ID NO:53, wherein mSDF-1 maintains chemoattractant activity for T cells and is inactivated by matrix metalloproteinase-2 (MMP-2) at a rate that is less than one-half of the rate of inactivation of native SDF-1; and
d) X p -mSDF-1 is a mutant form of said SDF-1 comprising the amino acid sequence of SEQ ID NO: 53, wherein Xe-mSDF-1 maintains chemoattractant activity for T cells, is inactivated by dipeptidyl peptidase IV (DPPIV) at a rate that is less than one-half of the rate at which native SDF-1 is inactivated, and is inactivated by MMP-2 at a rate that is less than one-half of the rate of inactivation of native SDF-1.
2. The isolated mutant SDF-1 peptide of claim 1 , wherein said mSDF-1 peptide or said X p -mSDF-1 peptide is SDF(S4V) consisting of SEQ ID NO:54.
3. An isolated mutant form of SDF-1 peptide comprising the mutant SDF-1 (mSDF-1) or X p -mSDF-1, wherein:
a) X is proteinogenic amino acid(s) or a protease protective organic group;
b) p is any integer from 1 to 4;
c) mSDF-1 is a mutant form of said SDF-1 comprising the amino acid sequence of SEQ ID NO:55, wherein mSDF-1 maintains chemoattractant activity for T cells and is inactivated by MMP-2 at a rate that is less than one-half of the rate of inactivation of native SDF-1; and
d) X p -mSDF-1 is a mutant form of said SDF-1 comprising the amino acid sequence of SEQ ID NO: 55, wherein X p -mSDF-1 maintains chemoattractant activity for T cells, is inactivated by DPPIV at a rate that is less than one-half of the rate at which native SDF-1 is inactivated, and is inactivated by MMP-2 at a rate that is less than one-half of the rate of inactivation of native SDF-1.
4. The isolated mutant SDF-1 peptide of claim 3 , wherein said mSDF-1 peptide or said Xp-mSDF-1 peptide is SDF(L5P) consisting of SEQ ID NO:56.
5. The isolated mutant SDF-1 peptide of claim 2 , wherein said isolated mutant SDF-1 peptide is an Xp-mSDF-1 peptide comprising the amino acid sequence of SEQ ID NO: 54, wherein X is a serine and p equals one.
6. A fusion protein comprising the formula: A-(L) n -(R) q , wherein: A is the isolated mutant SDF-1 peptide of any one of claims 2 - 5 , n is an integer from 0-3; q is an integer from 1-3; L is a linker sequence of 3-9 amino acids, and R is a self-assembling peptide as set forth in RARADADARARADADA (SEQ ID NO: 35).
7. The isolated mutant SDF-1 peptide of claim 1 , wherein said mSDF-1 peptide or said Xp-mSDF-1 peptide maintains chemoattractant activity for T cells of at least 10% that of native SDF-1 and is inactivated by MMP-2 at a rate that is less than one-fourth of the rate of inactivation of native SDF- 1.
8. The fusion protein of claim 6 , wherein n=1 and L is GGGGGG (SEQ ID NO:57).
9. The fusion protein of claim 8 , wherein A is the mSDF-1 peptide of SEQ ID NO:54.
10. The fusion protein of claim 9 , wherein q=1 and R is RARADADARARADADA (SEQ ID NO:35).
11. The fusion protein of claim 6 , wherein: A is an Xp-mSDF-1 peptide comprising the amino acid sequence of SEQ ID NO: 54, wherein X is a serine and p equals one; wherein n is an integer from 0-3; q=1; L is a linker sequence of 3-9 amino acids, and R is RARADADARARADADA (SEQ ID NO:35).
12. The fusion protein of claim 11 , wherein n=1 and L is GGGGGG (SEQ ID NO:57).
13. The fusion protein of claim 6 , wherein: A is an Xp-mSDF-1 peptide comprising the amino acid sequence of SEQ ID NO: 56, wherein X is a serine and p equals one; wherein n is an integer from 0-3; q=1; L is a linker sequence of 3-9 amino acids, and R is RARADADARARADADA (SEQ ID NO:35).
14. The fusion protein of claim 13 , wherein n=1 and L is GGGGGG (SEQ ID NO:57).
15. The isolated mutant SDF-1 peptide of claim 4 , wherein said isolated mutant SDF-1 peptide is an Xp-mSDF-1 peptide comprising the amino acid sequence of SEQ ID NO: 56, wherein X is a serine and p equals one.
16. The isolated mutant SDF-1 peptide of claim 9 , wherein said mSDF-1 peptide or said Xp-mSDF-1 peptide maintains chemoattractant activity for T cells of at least 10% that of native SDF-1 and is inactivated by MMP-2 at a rate that is less than one-fourth of the rate of inactivation of native SDF-1.