IP Library Granted Patent US 8,106,013
Granted Patent B2
US 8,106,013 · App. 12/299,881 · Granted Jan 31, 2012

ABC transporter ligand GATX1

Assignee: Georgia Tech Research Corporation
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Quick Facts
Patent No.
US 8,106,013
App. No.
12/299,881
Granted
Jan 31, 2012
Kind
B2
Abstract

Compositions and methods of using scorpion venom peptide that is a ligand for ABC transporters. One aspect provides a peptide having at least 80% sequence identity to SEQ ID NO: 1. The peptide Is believed to have a molecular mass of about 3.7 kDa and specifically interacts with cystic fibrosis transmembrane conductance regulator. Methods of treating a disorder or symptom of a disorder related to aberrant ABC transporter activity are also provided.

Claims (11)

1. A single polypeptide isolated from scorpion L. quinquestriatus hebraeus venom comprising the amino acid sequence of SEQ ID NO:1.

2. The polypeptide of claim 1 , wherein the polypeptide binds cystic fibrosis transmembrane conductance regulator.

3. The polypeptide of claim 2 , wherein the polypeptide interacts with cystic fibrosis transmembrane conductance regulator in the interburst state.

4. The polypeptide of claim 3 , wherein binding of the polypeptide to the cystic fibrosis transmembrane conductance regulator locks closed the cystic fibrosis transmembrane conductance regulator.

5. An isolated synthetic or recombinant polypeptide comprising the amino acid sequence of SEQ ID NO:1.

6. A pharmaceutical composition comprising an effective amount of the polypeptide according to claim 1 or 5 to reduce chloride transport through cystic fibrosis transmembrane conductance regulator and a pharmaceutically acceptable diluent, preservative, solubilizer, emulsifier, adjuvant or carrier.

7. A composition comprising the polypeptide of claim 1 or 5 .

8. An ex vivo method of reducing chloride transport through a cystic fibrosis transmembrane conductance regulator (CFTR) channel comprising contacting the CFTR channel with the polypeptide of claim 1 or 5 .

9. A method for treating a disorder or symptom of a disorder related to increased cystic fibrosis transmembrane conductance regulator (CFTR) activity comprising:

administering a therapeutically effective amount of the polypeptide according to claim 1 or 5 , wherein the disorder is diarrhea-predominant inflammatory bowel syndrome, autosomal dominant polycystic kidney disease (ADPKD), or secretory diarrhea.

10. An in vivo method of reducing chloride transport through cystic fibrosis transmembrane conductance regulator (CFTR) in a subject having a disorder related to increased CFTR activity, comprising administering to the polypeptide of claim 1 or 5 such that CFTR is contacted with the polypeptide, wherein the disorder is diarrhea-predominant inflammatory bowel syndrome, autosomal dominant polycystic kidney disease (ADPKD), or secretory diarrhea.

Assignments (2)
CONFIRMATORY LICENSE Recorded Jul 17, 2015
From: GEORGIA INSTITUTE OF TECHNOLOGY
To: NATIONAL SCIENCE FOUNDATION
Reel/Frame 036129/0682 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 4, 2009
From: MCCARTY, NAEL; FULLER, MATTHEW; KUBANEK, JULIA
To: GEORGIA TECH RESEARCH CORPORATION
Reel/Frame 023467/0245 →
Continuity (2)
Provisional Application 60801863 · May 19, 2006
Related Publication 20090203598A1 · Aug 13, 2009