Designer collagens and use thereof
The present disclosure provides synthetic collagen and methods of making and using synthetic collagen that include a synthetic collagen that facilitates wound closure comprising an isolated and purified triple helical backbone protein that facilitates wound closure comprising one or more alteration in a triple helical backbone protein sequence, that stabilize the isolated and purified triple helical backbone protein and does not disrupt an additional collagen ligand interaction; and one or more integrin binding motifs, wherein the isolated and purified triple helical backbone protein facilitates wound closure.
1. A synthetic collagen that facilitates wound closure comprising:
an isolated and purified triple helical backbone protein that facilitates the wound closure comprising:
one or more alterations in a triple helical backbone protein sequence comprising charged residues without hydroxyproline that stabilize the isolated and purified triple helical backbone protein, wherein the one or more alterations do not disrupt an additional collagen ligand interaction and do not bind or activate platelets; wherein the altered triple helical backbone protein sequence has been modified to comprise two or more GFPGER (SEP ID NO: 10) integrin binding motifs that binds an integrin α1, wherein the isolated and purified triple helical backbone protein facilitates the wound closure.
2. The synthetic collagen of claim 1 , wherein the isolated and purified triple helical backbone protein is produced in a prokaryotic expression system.
3. The synthetic collagen of claim 1 , wherein the triple helical backbone is derived from a Streptococcal protein.
4. The synthetic collagen of claim 1 wherein the synthetic collagen is formulated with a topical carrier to form a topical composition.
5. The synthetic collagen of claim 1 , wherein the collagen ligand is an integrin.
6. The synthetic collagen of claim 5 , wherein the collagen ligand is an integrin α1β1.
7. The synthetic collagen of claim 1 , wherein the isolated and purified triple helical backbone protein has a higher melting temperature than an unmodified triple helical backbone protein.
8. The synthetic collagen of claim 1 , wherein the isolated and purified triple helical backbone protein is supported by a matrix.
9. The synthetic collagen of claim 8 , wherein the matrix is a polymer matrix.
10. The synthetic collagen of claim 8 , wherein the polymer matrix is a Poly(ethylene glycol) hydrogel.
11. The synthetic collagen of claim 8 , wherein the matrix is an acellular derived mammalian matrix.
12. The synthetic collagen of claim 1 , wherein the isolated and purified triple helical backbone protein is formed into a vascular graft, a wound dressing, or a matrices for bone and cartilage regeneration.
13. The synthetic collagen of claim 1 , wherein the isolated and purified triple helical backbone protein is formed into a lumen of a vascular graft.
14. The synthetic collagen of claim 1 , wherein the isolated and purified triple helical backbone protein binds a fibronectin.
15. The synthetic collagen of claim 14 , wherein the fibronectin is in an acellular matrix derived from mammals.
16. A topical synthetic collagen composition that facilitates wound closure comprising:
a topical carrier;
a synthetic and isolated triple helical backbone protein that facilitates the wound closure disposed in the topical carrier, wherein the synthetic and isolated triple, helical backbone protein comprises:
one or more alteration in the triple helical backbone protein sequence, that stabilize the synthetic and isolated triple helical backbone protein and does not disrupt interaction of integrin α 1 β 1 or integrin α 2 β 1 with collagen and does not bind and activate platelets; wherein the altered triple helical backbone protein sequence has been modified to comprise two or more GFPGER (SEP ID NO: 10) repeats that are integrin binding motifs which bind integrin α 1 and have an increased binding affinity for the integrin.