IP Library Granted Patent US 9,527,890
Granted Patent B2
US 9,527,890 · App. 14/897,999 · Granted Dec 27, 2016

FC receptor (FcRn) binding peptides and uses thereof

Inventors: Richard S. Blumberg (Waltham, MA); Timo Rath (Cambridge, MA); Kristi Baker (Brookline, MA); Adam Mezo (Carmel, IN); Zachary Taylor (Crestview Hills, KY); Kevin McDonnell (Lexington, MA); Rosa Maria Silva Garcia Grenha (Arlington, MA)
C07K14/001C07K7/08C07K14/70535C07K14/765C12N15/1037G01N33/5023A61K38/00C07K2319/00C07K2319/31C07K2319/40
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Quick Facts
Patent No.
US 9,527,890
App. No.
14/897,999
Granted
Dec 27, 2016
Kind
B2
Abstract

The invention provided herein includes isolated polypeptides that specifically block the interaction between neonatal Fc receptor (FcRn) and albumin. Blocking the interaction treats diseases and conditions caused by increased amounts of albumin or modified albumin that possesses pathogenic properties wherein it is deemed desirable to decrease albumin levels. Accordingly, also provided are methods of using these isolated polypeptides to treat various diseases and conditions caused by increased amounts of albumin or modified albumin that possesses pathogenic properties. The invention provided herein also includes isolated polypeptides capable of binding to a non-IgG and non-albumin competitive site on an FcRn alpha 3 domain. These can be useful for tracking FcRn without inhibiting IgG or albumin binding or function. Accordingly, the invention also includes methods and systems to track FcRn without inhibiting IgG or albumin binding or function.

Claims (9)

1. An isolated polypeptide that specifically blocks the interaction between neonatal Fc receptor (FCRN) and albumin comprising at least one peptide subunit consisting of an amino acid sequence that is at least 90% identical to RYFCTKWKHGWCEEVGT (SEQ ID NO:1).

2. The isolated polypeptide of claim 1 , wherein the at least one peptide subunit consists of the amino acid sequence set forth in SEQ ID NO:1.

3. The isolated polypeptide of claim 1 , comprising two peptide subunits, wherein the peptide subunits consist of an amino acid sequence that is at least 90% identical to SEQ ID NO:1.

4. The isolated polypeptide of claim 1 , comprising four peptide subunits, wherein the peptide subunits consist of an amino acid sequence that is at least 90% identical to SEQ ID NO:1.

5. The isolated polypeptide of claim 3 , wherein the peptide subunits are linked by a linker.

6. The isolated polypeptide of claim 5 , wherein the linker is a peptide linker comprising 1-10 amino acids.

7. The isolated polypeptide of claim 5 , wherein the linker is a glycine linker comprising 1-10 glycine residues (SEQ ID NO: 14), or 1-10 glycine and serine residues (SEQ ID NO: 15).

8. The isolated polypeptide of claim 7 , wherein the glycine linker comprises 3-5 glycine residues (SEQ ID NO: 16), or 3-5 glycine and serine residues (SEQ ID NO: 17).

9. The isolated polypeptide of claim 5 , wherein the linker is formed from a polyethylene glycol (PEG) H—(O—CH 2 —CH 2 ) n —OH, wherein n is an integer from 2-12.

Assignments (4)
CONFIRMATORY LICENSE Recorded Dec 11, 2018
From: BRIGHAM AND WOMEN'S HOSPITAL
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 047768/0458 →
CHANGE OF NAME Recorded Dec 8, 2016
From: BIOGEN IDEC MA INC.
To: BIOGEN MA INC.
Reel/Frame 040866/0402 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 15, 2016
From: MEZO, ADAM; TAYLOR, ZACHARY; MCDONNELL, KEVIN
To: BIOGEN IDEC MA INC.
Reel/Frame 040328/0100 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 15, 2016
From: BLUMBERG, RICHARD S.; RATH, TIMO; BAKER, KRISTI; GRENHA, ROSA MARIA SILVA
To: THE BRIGHAM AND WOMEN'S HOSPITAL, INC
Reel/Frame 040328/0145 →
Continuity (2)
Provisional Application 61836279 · Jun 18, 2013
Related Publication 20160122394A1 · May 5, 2016