IP Library Granted Patent US 12,162,924
Granted Patent B2
US 12,162,924 · App. 17/554,650 · Granted Dec 10, 2024

Method for the design of fibrillar collagen-mimetic peptide self-assemblies

Inventors: Ronald T. Raines (Madison, WI); Ismet Tanrikulu (Madison, WI)
Assignee: WISCONSIN ALUMNI RESEARCH FOUNDATION
C07K14/78
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Quick Facts
Patent No.
US 12,162,924
App. No.
17/554,650
Granted
Dec 10, 2024
Kind
B2
Abstract

Novel synthetic human scale collagen triple helices assemblies are disclosed. Methods of making self-assembling collagen mimetic peptides that self-assemble into human scale collagen are also disclosed.

Claims (29)

1. A synthetic symmetrical triple helical collagen assembly comprising:

a plurality of self-assembling collagen mimetic peptides comprising Xaa-Yaa-Gly tripeptide repeats, wherein the number of tripeptide repeats (n T ) is 3v±1, wherein v is a positive integer, wherein the peptide is n residues in length, wherein n=n T ×3;

wherein the collagen mimetic peptides self-assemble with an n t -residue offset to form the symmetrical triple helical collagen assembly.

2. The synthetic symmetrical triple helical collagen assembly of claim 1 , wherein the collagen mimetic peptides comprise the tripeptides in the following sequence:

(POG) n (PKG/DOG) m (POG/DKG) p (DOG/PKG) q (POG) r wherein n, m, p, q, and r are selected from 0 or a positive integer of 1-10, and wherein n T =n+m+p+q+r=3v±1>0.

3. The synthetic symmetrical triple helical collagen assembly of claim 1 , wherein neighboring self-assembling collagen mimetic peptides of the triple helical collagen assembly are offset by Xaa-Yaa-Gly tripeptide repeats.

4. The synthetic symmetrical triple helical collagen assembly of claim 1 , wherein the Yaa amino acid of a K t Xaa-Yaa-Gly tripeptide repeat comprises an amino acid capable of charge pairing and the Xaa amino acid of a D t Xaa-Yaa-Gly tripeptide repeat comprises an amino acid capable of charge pairing with the Yaa amino acid of the K t Xaa-Yaa-Gly tripeptide repeat on a neighboring self-assembling collagen mimetic peptide of the triple helical collagen assembly, and wherein K t is a positive integer from 1 to nT and D t =(K t ±v+1) mod nT.

5. The synthetic symmetrical triple helical collagen assembly of claim 1 , comprising a charged block at an end of the triple helical collagen assembly.

6. The synthetic symmetrical triple helical collagen assembly of claim 5 , wherein the triple helical collagen assembly is stabilized by an interstrand interaction between the Yaa amino acid of the K t Xaa-Yaa-Gly tripeptide repeat and the Xaa amino acid of a D t Xaa-Yaa-Gly tripeptide repeat on the neighboring self-assembling collagen mimetic peptide of the triple helical collagen assembly.

7. The synthetic symmetrical triple helical collagen assembly of claim 6 , wherein the interstrand interaction comprises at least one interstrand salt bridge.

8. The synthetic symmetrical triple helical collagen assembly of claim 7 , wherein the at least one interstrand salt bridge is formed from a lysine residue in the Yaa position of the K t Xaa-Yaa-Gly tripeptide repeat and an aspartic acid residue in the Xaa position of the D t Xaa-Yaa-Gly tripeptide repeat on the neighboring self-assembling collagen mimetic peptide.

9. The synthetic symmetrical triple helical collagen assembly of claim 7 , wherein the at least one interstrand salt bridge comprises a first interstrand salt bridge and a second interstrand salt bridge, wherein the first interstrand salt bridge is formed from a lysine residue in the Yaa position of the K t Xaa-Yaa-Gly tripeptide repeat on a first strand and an aspartic acid residue in the Xaa position of the D t Xaa-Yaa-Gly tripeptide repeat on the neighboring self-assembling collagen mimetic peptide on a second strand and the second interstrand salt bridge is formed from a lysine residue in the Yaa position of the K t Xaa-Yaa-Gly tripeptide repeat on a second strand and an aspartic acid residue in the Xaa position of the D t Xaa-Yaa-Gly tripeptide repeat on the neighboring self-assembling collagen mimetic peptide on a third strand.

10. The synthetic symmetrical triple helical collagen assembly of claim 7 , wherein the at least one interstrand salt bridge is formed from a lysine residue in the Yaa position on a first strand and an aspartic acid residue in the Xaa position on a second strand at a three residue offset.

11. The synthetic symmetrical triple helical collagen assembly of claim 8 , wherein greater than about 90% of the available lysine residues and available aspartic acid residues are linked by an interstrand salt bridge.

12. The synthetic symmetrical triple helical collagen assembly of claim 1 , wherein nT is 3v+1.

13. The synthetic symmetrical triple helical collagen assembly of claim 1 , wherein nT is 3v−1.

14. The synthetic symmetrical triple helical collagen assembly of claim 1 , wherein v is 5.

15. The synthetic symmetrical triple helical collagen assembly of claim 14 , wherein the triple helical collagen assembly comprises a homotrimer wherein the homotrimer comprises about 4 salt bridges per about 14 residues.

16. The synthetic symmetrical triple helical collagen assembly of claim 1 , wherein the Xaa-Yaa-Gly tripeptide repeats comprises Xaa-Yaa-Gly tripeptide repeats of ProLysGly, AspHypGly, ProHypGly or combinations thereof.

17. The synthetic symmetrical triple helical collagen assembly of claim 1 , wherein the Xaa-Yaa-Gly tripeptide repeats are selected from the group consisting of POG, PKG, DOG, DKG and combinations thereof.

18. The synthetic symmetrical triple helical collagen assembly of claim 1 , wherein the each strand of the helix is at least about 500 residues.

19. The synthetic symmetrical triple helical collagen assembly of claim 1 , wherein the assembly is about 200 nm in length.

20. The synthetic symmetrical triple helical collagen assembly of claim 1 , wherein the assembly comprises a central Xaa-Yaa-Gly tripeptide repeat and Xaa of the central Xaa-Yaa-Gly tripeptide repeat is proline or aspartic acid and Yaa of the central Xaa-Yaa-Gly tripeptide repeat is lysine to reduce blunt end association.

21. The synthetic symmetrical triple helical collagen assembly of claim 1 , wherein the self-assembling collagen mimetic peptide comprises a terminal Xaa-Yaa-Gly tripeptide repeat and Yaa of the terminal Xaa-Yaa-Gly tripeptide repeat is hydroxyproline to reduce blunt end association.

22. The synthetic symmetrical triple helical collagen assembly of claim 1 , wherein the symmetrical triple helical collagen assembly has a melting temperature (Tm) of greater than about 37° C.

23. The synthetic symmetrical triple helical collagen assembly of claim 1 , wherein the symmetrical triple helical collagen assembly has a melting temperature (Tm) of greater than about 45° C.

24. The synthetic symmetrical triple helical collagen assembly of claim 1 , wherein the Xaa-Yaa-Gly tripeptide repeats comprises any one of sequence SEQ ID NO: 2-9, 10, 12, 14-18, 22, or 27-37.

25. The synthetic symmetrical triple helical collagen assembly of claim 1 , wherein the collagen mimetic peptides comprise the tripeptides in the following sequence:

(POG)n(PKG/DOG)m(POG/DKG)p (DOG/PKG)q(POG)r wherein n, m, p, q, and r are selected from 0 or a positive integer of 1-10, and wherein nT=n+m+p+q+r=3v±1>0.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 10, 2022
From: TANRIKULU, ISMET; RAINES, ROBERT
To: WISCONSIN ALUMNI RESEARCH FOUNDATION
Reel/Frame 058589/0431 →
Continuity (3)
Division 15622966 · Jun 14, 2017
Provisional Application 62350035 · Jun 14, 2016
Related Publication 20220112269A1 · Apr 14, 2022