Affibody-based dual affinity fusion proteins and uses thereof

Patent metadata

Field	Value
Publication number	US-2026070967-A1
Application number	US-202519324928-A
Country	US
Kind code	A1
Filing date	Sep 10, 2025
Priority date	Sep 10, 2024
Publication date	Mar 12, 2026
Grant date	—

Abstract

Provided are dual-affinity fusion proteins including an affibody domain specific for a therapeutic protein, and including a localization domain specific for a structural bone component. The therapeutic protein can include bone morphogenetic protein 2 (BMP-2), vascular endothelial growth factor (VEGF), fibroblast growth factor 2 (FGF-2), platelet-derived growth factor (PDGF), granulocyte-macrophage colony-stimulating factor (GM-CSF), interleukin-4 (IL-4), or glial derived neurotrophic factor (GDNF). Also provided are compositions that include the dual-affinity fusion proteins, affibodies and the corresponding therapeutic proteins, and/or a medical material used to treat a wound, or a bone or cartilage injury or disease. Also provided are methods of using the compositions, for example to treat bone injuries, bone diseases, cartilage injuries, cartilage diseases, and wounds. In some examples, the composition includes at least two different dual-affinity fusion proteins specific for the same therapeutic protein, but have different disassociation constants (K D ).

First claim

We claim:

1 . A dual-affinity fusion protein, comprising an affibody sequence, a linker, and a localization domain, wherein the affibody sequence is specific for a therapeutic protein, and the localization domain is specific for a structural bone component.

2 . The dual-affinity fusion protein of claim 1 , wherein the therapeutic protein is bone morphogenetic protein 2 (BMP-2), vascular endothelial growth factor (VEGF), fibroblast growth factor 2 (FGF-2), platelet-derived growth factor (PDGF), granulocyte macrophage colony stimulating factor (GM-CSF), or interleukin-4 (IL-4).

3 . The dual-affinity fusion protein of claim 1 , wherein the structural bone component is present in a collagen scaffold, collagen sponge, bone void filler, or bone graft.

4 . The dual-affinity fusion protein of claim 1 , wherein the structural bone component is collagen, a calcium phosphate, or a calcium sulphate.

5 . The dual-affinity fusion protein of claim 4 , wherein:
the collagen is Type I collagen, Type II collagen, or Type III collagen, or the calcium phosphate is hydroxyapatite (HA), β-tricalcium phosphate (β-TCP), α-tricalcium phosphate (α-TCP), calcium deficient hydroxyapatite (CDHA), tetracalcium phosphate (TTCP), amorphous calcium phosphate (ACP), dicalcium phosphate dihydrate (DCPD), or dicalcium phosphate anhydrous (DCPA).

6 . The dual-affinity fusion protein of claim 1 , wherein the linker is a flexible linker, a rigid linker, or a hybrid linker comprising a flexible and a rigid segments.

7 . The dual-affinity fusion protein of claim 1 , wherein the affibody sequence comprises at least 90% sequence identity to any one of SEQ ID NOs: 1-68 and 71-74, with or without the initial A.

8 . The dual-affinity fusion protein of claim 1 , wherein the localization domain comprises at least 90% sequence identity to any one of SEQ ID NOs: 75-79 and 127.

9 . The dual-affinity fusion protein of claim 1 , wherein the linker sequence comprises any one of SEQ ID NOs: 80-85 and 120-125.

10 . The dual-affinity fusion protein of claim 1 , wherein the affibody sequence is 58 to 65 amino acids in length.

11 . The dual-affinity fusion protein of claim 1 , wherein the affibody sequence comprises 1, 2, 3, 4, 5 or 6 conservative amino acid substitutions as compared to any of SEQ ID NOs: 1-68 and 71-74, with or without the initial A.

12 . The dual-affinity fusion protein of claim 1 , wherein the fusion protein comprises at least 90% sequence identity to any one of SEQ ID NOs: 87-112 and 126, or comprises 1, 2, 3, 4, 5 or 6 conservative amino acid substitutions as compared to any of SEQ ID NOs: 87-112 and 126.

13 . A composition comprising:
the dual-affinity fusion protein of claim 1 , and a therapeutic protein; wherein the affibody sequence in the dual-affinity fusion protein is specific for the therapeutic protein.

14 . The composition of claim 13 , wherein the dual-affinity fusion protein is non-covalently bound to the therapeutic protein through the affibody sequence.

15 . The composition of claim 13 , wherein the composition further comprises a structural bone component.

16 . The composition of claim 15 , wherein the dual-affinity fusion protein is non-covalently bound to the structural bone component through the localization domain.

17 . The composition of claim 13 , wherein the therapeutic protein is bone morphogenetic protein 2 (BMP-2), vascular endothelial growth factor (VEGF), fibroblast growth factor 2 (FGF-2), platelet-derived growth factor (PDGF), granulocyte macrophage colony stimulating factor (GM-CSF), or interleukin-4 (IL-4).

18 . The composition of claim 15 , wherein the structural bone component is present in a collagen scaffold, collagen sponge, bone void filler, or bone graft.

19 . The composition of claim 15 , wherein the structural bone component is collagen, a calcium phosphate, or a calcium sulphate.

20 . The composition of claim 19 , wherein:
the collagen is Type I collagen, Type II collagen, or Type III collagen, or the calcium phosphate is hydroxyapatite (HA), β-tricalcium phosphate (β-TCP), α-tricalcium phosphate (α-TCP), calcium deficient hydroxyapatite (CDHA), tetracalcium phosphate (TTCP), amorphous calcium phosphate (ACP), dicalcium phosphate dihydrate (DCPD), or dicalcium phosphate anhydrous (DCPA).

21 . A method of treating a wound, or a bone or cartilage injury or disease in a subject, comprising:
administering an effective amount of the dual-affinity fusion protein of claim 1 to the subject, thereby treating the bone or cartilage injury or disease.

22 . The method of claim 21 , wherein the bone injury or disease is a bone fracture or a degenerative bone disease.

23 . The method of claim 21 , wherein the administering is surgical administration or injection.

Assignees

• Univ Oregon

Inventors

• Singhal Malvika
• Hettiaratchi Marian H

Classifications

• C07K14/475

  Growth factors; Growth regulators · CPC title

• C07K2319/33

  fusions for targeting to specific cell types, e.g. tissue specific targeting, targeting of a bacterial subspecies · CPC title

• C07K14/51

  Bone morphogenetic factor; Osteogenins; Osteogenic factor; Bone-inducing factor · CPC title

• C07K2319/00

  Fusion polypeptide · CPC title

• C07K2319/01

  containing a localisation/targetting motif · CPC title