IP Library › Granted Patent US 11,203,630
Granted Patent B2
US 11,203,630 · App. 16/549,462 · Granted Dec 21, 2021

Serum albumin-binding fibronectin type III domains

Inventors: Tracy S. Mitchell (Andover, MA); Michael L. Gosselin (Boston, MA); Dasa Lipovsek (Pepperell, MA); Rex Parker (Titusville, NJ); Ray Camphausen (Wayland, MA); Jonathan H. Davis (Madison, WI); David Fabrizio (South Hamilton, MA)
Assignee: BRISTOL-MYERS SQUIBB COMPANY
C07K14/78A61K47/64A61K38/00C07K2319/00C07K2319/70
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Quick Facts
Patent No.
US 11,203,630
App. No.
16/549,462
Granted
Dec 21, 2021
Kind
B2
Abstract

The present invention relates to polypeptides which include tenth fibronectin type III domains ( 10 Fn3) that binds to serum albumin, with south pole loop substitutions. The invention further relates to fusion molecules comprising a serum albumin-binding 10 Fn3 joined to a heterologous protein for use in diagnostic and therapeutic applications.

Claims (9)

1. An isolated nucleic acid molecule encoding a polypeptide comprising a fibronectin type III tenth domain ( 10 Fn3) wherein the CD loop corresponding to the CD loop of the wild-type 10 Fn3 domain set forth in SEQ ID NO: 1 is replaced by an amino acid sequence selected from the group consisting of SEQ ID NOs: 101-125, and wherein the polypeptide binds to human serum albumin and to one or more of rhesus serum albumin, cynomolgus serum albumin, mouse serum albumin, and rat serum albumin.

2. An expression vector comprising the nucleic acid of claim 1 .

3. A cell comprising a nucleic acid molecule of claim 1 .

4. A method of producing a polypeptide comprising a fibronectin type III tenth ( 10 Fn3) domain, wherein the CD loop corresponding to the CD loop of the wild-type 10 Fn3 domain set forth in SEQ ID NO: 1 is replaced by an amino acid sequence selected from the group consisting of SEQ ID NOs: 101-125, and wherein the polypeptide binds to human serum albumin and d) one or more of rhesus serum albumin, cynomolgus serum albumin, mouse serum albumin, and rat serum albumin, the method comprising culturing a cell comprising a nucleic acid encoding the polypeptide under conditions suitable for expressing the polypeptide, and purifying the polypeptide.

5. The nucleic acid of claim 1 , wherein the polypeptide comprises an amino acid sequence selected from the group consisting of SEQ 11) NOs: 23-30, 32-40, 42-100, 168-169, 184-191, 193-201, 203-209, 235-242, 243-252 and 254-261.

6. The nucleic acid of claim 1 , wherein the polypeptide is a fusion polypeptide comprising a heterologous protein.

7. The nucleic acid of claim 6 , wherein the heterologous protein is a therapeutic moiety.

8. The nucleic acid of claim 6 , wherein the heterologous protein is a polypeptide comprising a 10 Fn3 domain.

9. The nucleic acid of claim 8 , wherein the 10 Fn3 domain binds to a target protein other than serum albumin.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 11, 2020
From: MITCHELL, TRACY S; GOSSELIN, MICHAEL L.; LIPOVSEK, DASA; PARKER, REX; CAMPHAUSEN, RAY; DAVIS, JONATHAN; FABRIZIO, DAVID
To: BRISTOL-MYERS SQUIBB COMPANY
Reel/Frame 053750/0064 →
Continuity (3)
Division 15127166
Provisional Application 61968181 · Mar 20, 2014
Related Publication 20200048328A1 · Feb 13, 2020
Cited By (1)
US 12,534,511