IP Library Granted Patent US 10,385,115
Granted Patent B2
US 10,385,115 · App. 15/561,799 · Granted Aug 20, 2019

Fibronectin type III domain-based fusion proteins

Inventors: Ashutosh Chilkoti (Durham, NC); Mandana Manzari (Durham, NC); Mareva Fevre (San Jose, CA)
Assignee: Duke University
C07K14/78A61K9/0019A61P35/00A61K38/00C07K2319/00C07K2319/01C07K2319/74
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Quick Facts
Patent No.
US 10,385,115
App. No.
15/561,799
Granted
Aug 20, 2019
Kind
B2
Abstract

Provided herein are fusion proteins including at least one binding polypeptide and at least one unstructured polypeptide. The fusion protein may further include at least one linker. Further provided are methods for determining the presence of a target in a sample, methods of treating a disease, methods of diagnosing a disease in a subject, and methods of determining the effectiveness of a treatment for a disease in a subject. The methods may include administering to the subject an effective amount of the fusion protein.

Claims (15)

1. A multivalent fusion protein comprising at least one Fibronectin type III (FnIII) domain that binds TNF-related apoptosis-inducing ligand receptor 2 (TRAILR-2) and comprises SEQ ID NO: 1, and at least one elastin-like polypeptide (ELP) comprising (VPGXG) n (SEQ ID NO: 19), wherein X is any amino acid except proline and n is an integer greater than or equal to 1, and wherein the ELP has a transition temperature (T t ) of about 10° C. to about 50° C.

2. The multivalent fusion protein of claim 1 , wherein n is 60, 120, or 180.

3. The multivalent fusion protein of claim 1 , wherein X is valine.

4. The multivalent fusion protein of claim 1 , wherein the multivalent fusion protein comprises a plurality of the FnIII domain.

5. The multivalent fusion protein of claim 4 , wherein the multivalent fusion protein comprises 2, 4, or 6 FnIII domains.

6. The multivalent fusion protein of claim 4 , wherein the multivalent fusion protein further comprises a linker positioned between at least two adjacent FnIII domains.

7. The multivalent fusion protein of claim 6 , wherein the linker comprises at least one glycine and at least one serine.

8. The multivalent fusion protein of claim 7 , wherein the linker comprises an amino acid sequence consisting of SEQ ID NO: 3 ((Gly 4 Ser) 3 ).

9. The multivalent fusion protein of claim 6 , wherein the linker comprises an amino acid sequence consisting of SEQ ID NO: 4.

10. A method for treating cancer in a subject in need thereof, the method comprising administering to the subject an effective amount of the multivalent fusion protein of claim 1 .

11. The method of claim 10 , wherein the cancer comprises colorectal adenocarcinoma.

12. The method of claim 10 , wherein the multivalent fusion protein is administered intravenously, intraarterially, or intraperitoneally to the subject.

13. The method of claim 10 , wherein the multivalent fusion protein is administered intratumorally.

14. The method of claim 10 , wherein the multivalent fusion protein forms a depot upon administration to the subject.

15. The method of claim 10 , wherein the multivalent fusion protein is administered in a controlled release formulation.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 26, 2017
From: CHILKOTI, ASHUTOSH; MANZARI, MANDANA; FEVRE, MAREVA
To: DUKE UNIVERSITY
Reel/Frame 043705/0281 →
Continuity (2)
Provisional Application 62138847 · Mar 26, 2015
Related Publication 20180258157A1 · Sep 13, 2018
Cited By (7)
US 12,257,308 US 12,269,847 US 12,296,018 US 12,594,347 US 12,630,590 US 12,637,664 US 12,692,483