IP Library Granted Patent US 8,691,766
Granted Patent B2
US 8,691,766 · App. 13/368,968 · Granted Apr 8, 2014

Biglycan and related therapeutics and methods of use

Inventors: Justin R. Fallon (Providence, RI); Beth A. McKechnie (North Attleboro, MA); Michael Rafii (San Diego, CA); Hilliary Creely (Providence, RI); Mark A. Bowe (Damascus, MD); Alison R. Amenta (Pawtucket, RI); Mary Lynn Mercado (Robbinsville, NJ); Hiroki Hagiwara (Tokyo, JP)
Assignee: Brown University Research Foundation
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Quick Facts
Patent No.
US 8,691,766
App. No.
13/368,968
Granted
Apr 8, 2014
Kind
B2
Abstract

The invention provides compositions and methods for treating, preventing, and diagnosing diseases or conditions associated with an abnormal level or activity of biglycan; disorders associated with an unstable cytoplasmic membrane, due, e.g., to an unstable dystrophin associated protein complex (DAPC); disorders associated with abnormal synapses or neuromuscular junctions, including those resulting from an abnormal MuSK activation or acetylcholine receptor (AChR) aggregation. Example of diseases include muscular dystrophies, such as Duchenne's Muscular Dystrophy, Becker's Muscular Dystrophy, neuromuscular disorders and neurological disorders.

Claims (10)

1. A method for stabilizing dystrophin-associated protein complexes (DAPCs) on the surface of a cell, comprising contacting the cell with an effective amount of a biglycan therapeutic, such that the DAPCs are stabilized, wherein the biglycan therapeutic is a polypeptide comprising a biglycan amino acid sequence which is at least about 90% identical to amino acids 38-365 of SEQ ID NO: 9.

2. The method of claim 1 , wherein the biglycan therapeutic binds to Muscle-specific kinase (MuSK) on the cell.

3. The method of claim 1 , wherein the biglycan therapeutic binds to a α-sarcoglycan and/or γ-sarcoglycan on the cell.

4. The method of claim 1 , wherein the biglycan therapeutic induces phosphorylation of sarcoglycans on a cell membrane.

5. The method of claim 1 , wherein the biglycan therapeutic upregulates utrophin levels in the cell.

6. The method of claim 1 , wherein the biglycan amino acid sequence comprises one or more motifs of 24 consecutive amino acids in the Leucine Rich Repeat (LLR) of SEQ ID NO: 9.

7. The method of claim 1 , wherein the polypeptide is derivatized with one or more glycosaminoglycan (GAG) side chains.

8. The method of claim 1 , wherein the biglycan amino acid sequence is at least about 95% identical to amino acids 38-365 of SEQ ID NO: 9.

9. The method of claim 1 , wherein the biglycan amino acid sequence is encoded by a nucleic acid which hybridizes under stringent conditions of 6.0×sodium chloride/sodium citrate (SSC) at about 45° C. to a complementary strand of SEQ ID NO: 8.

10. The method of claim 1 , wherein the cell is a muscle cell.

Assignments (2)
CONFIRMATORY LICENSE Recorded Dec 7, 2015
From: BROWN UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 037224/0226 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 11, 2012
From: FALLON, JUSTIN R.; MCKECHNIE, BETH; RAFII, MICHAEL; CREELY, HILLIARY; BOWE, MARK A.; AMENTA, ALISON; MERCADO, MARY LYNN; HAGIWARA, HIROKI
To: BROWN UNIVERSITY RESEARCH FOUNDATION
Reel/Frame 028195/0011 →
Continuity (6)
Continuation 12498172 · Jul 6, 2009
Division 10081736 · Feb 20, 2002
Continuation In Part 09715836 · Nov 17, 2000
Provisional Application 60166253 · Nov 18, 1999
Provisional Application 60270053 · Feb 20, 2001
Related Publication 20120245095A1 · Sep 27, 2012