IP Library Granted Patent US 8,420,098
Granted Patent B2
US 8,420,098 · App. 13/085,864 · Granted Apr 16, 2013

Fibronectin based scaffold domain proteins that bind to PCSK9

Inventors: Ray Camphausen (Wayland, MA); Jonathan H. Davis (Auburndale, MA); Sharon T. Cload (Cambridge, MA); Fabienne M. Denhez (Arlington, MA); Amna Saeed-Kothe (West Roxbury, MA); Dasa Lipovsek (Cambridge, MA); Ching-Hsiung Frederick Lo (Pennington, NJ); Chee Meng Low (Allston, MA); Bowman Miao (Churchville, PA); Tracy S. Mitchell (Billerica, MA); Rex A. Parker (Titusville, NJ); Ginger C. Rakestraw (Cambridge, MA); Katie A. Russo (Watertown, MA); Doree F. Sitkoff (Dresher, PA)
Assignee: Bristol-Myers Squibb Company
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Quick Facts
Patent No.
US 8,420,098
App. No.
13/085,864
Granted
Apr 16, 2013
Kind
B2
Abstract

The present invention relates to fibronectin based scaffold domain proteins that bind PCSK9. The invention also relates to the use of the innovative proteins in therapeutic applications to treat atherosclerosis, hypercholesterolemia and other cholesterol related diseases. The invention further relates to cells comprising such proteins, polynucleotides encoding such proteins or fragments thereof, and to vectors comprising the polynucleotides encoding the innovative protein.

Claims (8)

1. An isolated polypeptide comprising a fibronectin type III tenth ( 10 Fn3) domain wherein the 10 Fn3 has a BC, DE and FG loop, and wherein the BC loop comprises SEQ ID NO:14, the DE comprises SEQ ID NO:25 and the FG loop comprises SEQ ID NO:37, and wherein the polypeptide binds proprotein convertase subtilisin kexin type (PCSK9).

2. The isolated polypeptide of claim 1 , wherein the polypeptide binds PCSK9 with a K D of less than 500 nM.

3. The isolated polypeptide of claim 1 , further comprising one or more pharmacokinetic (PK) moieties selected from the group consisting of polyethylene glycol, sialic acid, Fc, Fc fragment, transferring, serum albumin, a serum albumin binding protein, and a serum immunoglobulin binding protein.

4. A pharmaceutically acceptable composition comprising the polypeptide of claim 1 .

5. An isolated polypeptide comprising a 10 Fn3 domain wherein the isolated polypeptide comprises SEQ ID NO:82, and wherein the isolated polypeptide binds PCSK9.

6. The isolated polypeptide of claim 5 , wherein the polypeptide binds PCSK9 with a K D of less than 500 nM.

7. The isolated polypeptide of claim 5 , further comprising one or more pharmacokinetic (PK) moieties selected from the group consisting of polyethylene glycol, sialic acid, Fc, Fc fragment, transferring, serum albumin, a serum albumin binding protein, and a serum immunoglobulin binding protein.

8. A pharmaceutically acceptable composition comprising the polypeptide of claim 5 .

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 8, 2011
From: CAMPHAUSEN, RAY; DAVIS, JONATHAN H.; CLOAD, SHARON T.; DENHEZ, FABIENNE M.; SAEED-KOTHE, AMNA; LIPOVSEK, DASA; LO, CHING-HSIUNG FREDERICK; LOW, CHEE MENG; MIAO, BOWMAN; MITCHELL, TRACY S.; PARKER, REX A.; RAKESTRAW, GINGER C.; RUSSO, KATIE A.; SITKOFF, DOREE F.
To: BRISTOL-MYERS SQUIBB COMPANY
Reel/Frame 026560/0527 →
Continuity (3)
Provisional Application 61323562 · Apr 13, 2010
Provisional Application 61330731 · May 3, 2010
Related Publication 20120094909A1 · Apr 19, 2012