IP Library Granted Patent US 7,985,554
Granted Patent B2
US 7,985,554 · App. 11/546,880 · Granted Jul 26, 2011

Botulinum neurotoxin A receptor and the use thereof

Assignee: Wisconsin Alumni Research Foundation
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Quick Facts
Patent No.
US 7,985,554
App. No.
11/546,880
Granted
Jul 26, 2011
Kind
B2
Abstract

The present invention is based on the identification of synaptic vessel glycoprotein SV2 as the BoNT/A receptor and the further identification of various BoNT/A-binding fragments of SV2. The disclosure here provides new tools for diagnosing and treating botulism.

Claims (19)

1. An isolated polypeptide comprising an amino acid sequence selected from (i) amino acids 529-562 of rat SV2C (SEQ ID NO:6), (ii) amino acids 529-562 of human SV2C (SEQ ID NO:18), (iii) amino acids 486 to 519 of rat SV2B (SEQ ID NO:4), (iv) amino acids 486 to 519 of mouse SV2B (SEQ ID NO:10), (v) amino acids 486 to 519 of human SV2B (SEQ ID NO:16), (vi) amino acids 543 to 576 of rat SV2A (SEQ ID NO:2), (vii) amino acids 454-546 of rat SV2C (SEQ ID NO:6), (viii) amino acids 454-546 of human SV2C (SEQ ID NO:18), (ix) amino acids 411 to 503 of rat SV2B (SEQ ID NO:4), (x) amino acids 411 to 503 of human SV2B (SEQ ID NO:16), (xi) amino acids 468 to 560 of rat SV2A (SEQ ID NO:2), (xii) amino acids 468 to 560 of human SV2A (SEQ ID NO:14), and (xiii) an amino acid sequence that is at least 95% identical to (iii), (iv), (v), (ix), or (x) and is capable of binding to botulinum neurotoxin A (BoNT/A), with the proviso that a polypeptide comprising a full length SV2 protein, a polypeptide consisting of an SV2 luminal domain, and a polypeptide comprising an SV2 luminal domain wherein the domain is flanked at one or both ends by a non-native flanking amino acid sequence are excluded.

2. The isolated polypeptide of claim 1 , wherein the polypeptide is soluble in an aqueous solvent.

3. The isolated polypeptide of claim 1 , wherein the polypeptide has no more than 128 amino acids.

4. An isolated polypeptide consisting of an amino acid sequence selected from (i) amino acids 529-562 of rat SV2C (SEQ ID NO:6), (ii) amino acids 529-562 of mouse SV2C (SEQ ID NO:12), (iii) amino acids 529-562 of human SV2C (SEQ ID NO:18), (iv) amino acids 486 to 519 of rat SV2B (SEQ ID NO:4), (v) amino acids 486 to 519 of mouse SV2B (SEQ ID NO:10), (vi) amino acids 486 to 519 of human SV2B (SEQ ID NO:16), (vii) amino acids 543 to 576 of rat SV2A (SEQ ID NO:2), (viii) amino acids 543 to 576 of human SV2A (SEQ ID NO:14), (ix) amino acids 529-566 of rat SV2C (SEQ ID NO:6), (x) amino acids 529-566 of mouse SV2C (SEQ ID NO:12), (xi) amino acids 529-566 of human SV2C (SEQ ID NO:18), (xii) amino acids 486 to 523 of rat SV2B (SEQ ID NO:4), (xiii) amino acids 486 to 523 of mouse SV2B (SEQ ID NO:10), (xiv) amino acids 486 to 523 of human SV2B (SEQ ID NO:16), (xv) amino acids 543 to 580 of rat SV2A (SEQ ID NO:2), (xvi) amino acids 543 to 580 of human SV2A (SEQ ID NO:14), (xvii) amino acids 454-546 of rat SV2C (SEQ ID NO:6), (xviii) amino acids 454-546 of mouse SV2C (SEQ ID NO:12), (xix) amino acids 454-546 of human SV2C (SEQ ID NO:18), (xx) amino acids 411 to 503 of rat SV2B (SEQ ID NO:4), (xxi) amino acids 411 to 503 of human SV2B (SEQ ID NO:16), (xxii) amino acids 468 to 560 of rat SV2A (SEQ ID NO:2), (xxiii) amino acids 468 to 560 of human SV2A (SEQ ID NO:14), and (xxiv) an amino acid sequence that is at least 95% identical to (iv), (v), (vi), (xii), (xiii), (xiv), (xx), or (xxi) and is capable of binding to botulinum neurotoxin A (BoNT/A).

5. A method for identifying an agent that can block binding between BoNT/A and an SV2 protein, the method comprising the steps of:

measuring binding between BoNT/A and a polypeptide that comprises the polypeptide of claim 1 in the presence of a test agent; and

comparing the binding to that of a control measured under the same conditions but in the absence of the test agent, wherein a lower than control binding indicates that the agent can block binding between BoNT/A and the SV2 protein.

6. The method of claim 5 , wherein all steps are performed in vitro.

7. The method of claim 5 , wherein the polypeptide is provided on a cell surface and the cell is exposed to the test agent.

8. The method of claim 7 , wherein the binding between BoNT/A and the polypeptide is measured indirectly by monitoring the entry of BoNT/A into the cell.

9. A method for identifying an agent that can bind to a BoNT/A-binding sequence of an SV2 protein, the method comprising the steps of:

exposing a polypeptide that comprises the polypeptide of claim 1 to a test agent; and

determining whether the agent binds to the polypeptide.

10. The method of claim 9 , wherein all steps are carried out in vitro.

11. The method of claim 9 , where the polypeptide is provided and exposed to a test agent in a cell.

12. A method for detecting BoNT/A or Clostridium botulinum comprising the steps of:

exposing a sample suspected of containing BoNT/A to a polypeptide that comprises the polypeptide of claim 1 ;

optionally, exposing the sample to a ganglioside; and

detecting binding of the polypeptide to BoNT/A.

Assignments (3)
CONFIRMATORY LICENSE Recorded Feb 28, 2011
From: WISCONSIN ALUMNI RESEARCH FOUNDATION
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 025854/0738 →
EXECUTIVE ORDER 9424, CONFIRMATORY LICENSE Recorded Dec 18, 2008
From: UNIVERSITY OF WISCONSIN-MADISON
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 022001/0567 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 6, 2006
From: CHAPMAN, EDWIN R.; DONG, MIN
To: WISCONSIN ALUMNI RESEARCH FOUNDATION
Reel/Frame 018589/0111 →
Continuity (2)
Provisional Application 60726879 · Oct 14, 2005
Related Publication 20100249372A1 · Sep 30, 2010