Potent compstatin analogs
View Patent ↗Compounds comprising peptides and peptidomimetics capable of binding C3 protein and inhibiting complement activation are disclosed. These compounds display greatly improved complement activation-inhibitory activity as compared with currently available compounds.
1. A compound that inhibits complement activation, comprising a peptide having a sequence:
(SEQ ID NO: 26)
Xaa1-Cys-Val-Xaa2-Gln-Asp-Xaa3-Gly-Xaa4-His-Arg-
Cys-Xaa5;
wherein:
Xaa1 is Ile, Val, Leu, Ac-Ile, Ac-Val, Ac-Leu or a dipeptide comprising Gly-Ile;
Xaa2 is Trp or an analog of Trp, wherein the analog of Trp has increased hydrophobic character as compared with Trp, with the proviso that, if Xaa3 is Trp, Xaa2 is the analog of Trp comprising 5-fluoro-l-tryptophan, or 6-fluoro-l-tryptophan, or 5-methoxytryptophan, or 5-methyltryptophan, or 1-methyltryptophan, or 1-formyltryptophan;
Xaa3 is Trp or an analog of Trp comprising a chemical modification to its indole ring wherein the chemical modification increases the hydrogen bond potential of the indole ring;
Xaa4 is His, Ala, Phe or Trp;
Xaa5 is L-Thr, D-Thr, Ile, Val, Gly, a dipeptide comprising Thr-Asn or Thr-Ala, or a tripeptide comprising Thr-Ala-Asn, wherein a carboxy terminal —OH of any of the L-Thr, D-Thr, Ile, Val, Gly or Asn optionally is replaced by —NH2; and
the two Cys residues are joined by a disulfide bond.
2. The compound of claim 1 , wherein Xaa3 is an analog of Trp and Xaa2 is an analog of Trp that participates in a nonpolar interaction with C3.
3. The compound of claim 2 , wherein Xaa3 is an analog of Trp and that participates in a hydrogen bond with C3, and Xaa2 is an analog of Trp that participates in a nonpolar interaction with C3.
4. The compound of claim 1 , wherein Xaa3 is an analog of Trp that participates in a hydrogen bond with C3.
5. The compound of claim 1 , wherein Xaa3 is an analog of Trp, and Xaa2 is an analog of Trp comprising halogenated tryptophan.
6. The compound of claim 5 , wherein the halogenated tryptophan is 5-fluoro-1-tryptophan, or 6-fluoro-1-tryptophan.
7. The compound of claim 1 , wherein Xaa3 is an analog of Trp, and Xaa2 is an analog of Trp comprising a lower alkoxy or lower alkyl substituent at the 1 or 5 position of tryptophan.
8. The compound of claim 7 , wherein the analog of Trp of Xaa2 is 5-methoxytryptophan or 5-methyltryptophan or 1-methyltryptophan or 1-formyltryptophan.
9. The compound of claim 1 , wherein Xaa3 is an analog of Trp, and Xaa2 is an analog of Trp comprising a lower alkanoyl or lower alkyl substituent at the 1 position of tryptophan.
10. The compound of claim 9 , wherein the analog of Trp of Xaa2 is 1-methyltryptophan or 1-formyltryptophan.
11. The compound of claim 1 , wherein the analog of Trp of Xaa3 comprises a halogenated tryptophan.
12. The compound of claim 11 , wherein the halogenated tryptophan is 5-fluoro-1-tryptophan, or 6-fluoro-l-tryptophan.
13. The compound of claim 1 , wherein Xaa4 is Ala.
14. The compound of claim 1 , wherein Xaa2 comprises a lower alkanoyl or lower alkyl substituent at the 1 position of tryptophan, Xaa3 optionally comprises a halogenated tryptophan and Xaa4 comprises Alanine, with the proviso that, if Xaa3 is Trp instead of halogenated tryptophan, Xaa2 is an analog of Trp comprising 1-methyltryptophan, or 1-formyltryptophan.
15. The compound of claim 14 , wherein Xaa2 is 1-methyltryptophan or 1-formyltryptophan and Xaa3 optionally comprises 5-fluoro-1-tryptophan.
16. The compound of claim 1 , comprising any of SEQ ID NOS: 16 -25.
17. The compound of claim 1 , which comprises a peptide produced by expression of a polynucleotide encoding the peptide.
18. The compound of claim 1 , wherein the compound is produced at least in part by peptide synthesis.
19. The compound of claim 16 , comprising any one of SEQ ID NOS: 23, 24 or 25.
20. The compound of claim 1 , wherein the compound is PEGylated.
21. The compound of claim 20 , comprising SEQ ID NO:36.
22. The compound of claim 1 , further comprising an additional peptide component that extends the in vivo retention of the compound.
23. The compound of claim 22 , wherein the additional peptide component is an albumin binding peptide.
24. The compound of claim 23 , comprising SEQ ID NO:39.
25. The compound of claim 1 , which binds C3 and inhibits complement activation with at least 100-fold greater activity than does a peptide comprising SEQ ID NO:1 under equivalent assay conditions.