Modified gal-1 proteins and uses thereof
View Patent ↗Described herein are modified gal1 monomers that can contain one or more mutated cysteines and/or can be pegylated. Also described herein are modified gal1 dimers, trimers, and tetramers that can contain one or more modified gal1 monomers as described herein. Also described herein are pharmaceutical formulations containing a modified gal1 monomer, dimer, trimer, and/or tetramer. Also described herein are methods of making the modified gal1 polypeptides and complexes thereof. Also described herein are methods of using the modified gal1 polypeptides and complexes thereof.
1. A modified gal1 polypeptide comprising:
at least three amino acid mutations as compared to SEQ ID NO: 1, wherein the at least three amino acid mutations comprise three mutations selected from the group consisting of: C2S, C16S, C88S, and C130S, and wherein at least one of the cysteine residues selected from C2, C16, C88, and C130 is unmodified.
2. The modified gal1 polypeptide of claim 1 , wherein the at least three amino acid mutations comprise C2S, C16S, and C88S, and wherein C130 is unmodified.
3. The modified gal1 polypeptide of claim 1 , wherein the modified gal1 polypeptide is resistant to oxidative environments.
4. The modified gal1 polypeptide of claim 3 , wherein the modified gal1 polypeptide has an amino acid sequence that is 90-100% identical to SEQ ID NO: 7.
5. The modified gal1 polypeptide of claim 1 , wherein the modified gal1 polypeptide has an amino acid sequence that is 90-100% identical to SEQ ID NO: 7.
6. A pharmaceutical formulation comprising a modified gal1 polypeptide as in claim 1 and a pharmaceutically acceptable carrier.
7. A method comprising:
administering an amount of a modified gal1 polypeptide as in claim 1 to a subject.
8. The method of claim 7 , wherein the subject has an inflammatory disease, chronic inflammatory disease, autoimmune disease, or a symptom thereof.
9. A polynucleotide comprising a sequence that encodes a modified gal1 polypeptide as in claim 1 .
10. The polynucleotide of claim 9 , wherein the polynucleotide is about 98 to about 100 percent identical to SEQ ID NO: 8.
11. The modified gal1 polypeptide of claim 1 , wherein the modified gal1 polypeptide has an amino acid sequence that is 100% identical to SEQ ID NO: 11.
12. A modified gal1 dimer comprising two crosslinked modified gal1 polypeptides of claim 1 .
13. A modified gal1 tetramer comprising four crosslinked modified gal1 polypeptides of claim 1 .
14. A pharmaceutical formulation comprising the modified gal1 dimer of claim 12 and a pharmaceutically acceptable carrier.
15. A pharmaceutical formulation comprising the modified gal1 tetramer of claim 13 and a pharmaceutically acceptable carrier.
16. A method comprising administering the modified gal1 dimer of claim 12 to a subject.
17. A method comprising administering the modified gal1 tetramer of claim 13 to a subject.
18. The method of claim 16 , wherein the subject has an inflammatory disease, chronic inflammatory disease, autoimmune disease, or a symptom thereof.
19. The method of claim 17 , wherein the subject has an inflammatory disease, chronic inflammatory disease, autoimmune disease, or a symptom thereof.