IP Library Granted Patent US 7,618,793
Granted Patent B2
US 7,618,793 · App. 10/970,741 · Granted Nov 17, 2009

Identifying agents for decreasing cellular toxicity associated with huntingin polypeptide

Assignee: The Regents of the University of Washington
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Quick Facts
Patent No.
US 7,618,793
App. No.
10/970,741
Granted
Nov 17, 2009
Kind
B2
Abstract

Methods of screening candidate agents to identify potential therapeutic agents for the treatment of a neurodegenerative disease, such as Huntington's Disease and Parkinson's Disease and methods for identifying a mutation in, or changes in expression of, a gene associated with neurodegenerative disease, such as Huntington's Disease and Parkinson's Disease, are provided.

Claims (15)

1. A method of identifying an agent for decreasing cellular toxicity associated with huntingtin polypeptide, comprising:

contacting a first yeast cell with a candidate agent, wherein the first cell expresses (i) a huntingtin polypeptide comprising an expanded polyQ repeat with at least 103 consecutive glutamine residues and (ii) a wild-type BNA4 gene, wherein expression of the huntingtin polypeptide is toxic to the cell;

contacting a second yeast cell with the candidate agent, wherein the second cell expresses the huntingtin polypeptide and does not express the wild-type BNA4 gene; and

determining for the first and second cells the level of cell viability relative to a cell that does not express the huntingtin polypeptide and formation of inclusion bodies in the cell,

whereby if the first cell (a) exhibits a decrease of cell viability or formation of inclusion bodies relative to a control cell that has not been contacted with the candidate agent and (b) does not exhibit a decrease of cell viability or formation of inclusion bodies relative to the second cell, the agent is identified as an agent for decreasing cellular toxicity associated with huntingtin polypeptide.

2. The method of claim 1 , wherein the second cell contains a null allele of the wild-type BNA4 gene.

3. The method of claim 1 , wherein the second cell has a deletion of the wild-type BNA4 gene.

4. The method of claim 1 , wherein the yeast cell is a Saccharomyces cerevisiae cell.

5. The method of claim 1 , wherein the candidate agent is a small molecule, a nucleic acid, a proteinaceous agent, or a peptidomimetic.

6. The method of claim 1 , wherein the candidate agent is a synthetic compound.

7. The method of claim 1 , wherein the candidate agent is a natural compound.

8. The method of claim 1 , wherein the contacting the cell with the candidate agent comprises transformation or culturing the cell in media containing the candidate agent.

9. The method of claim 1 , wherein the huntingtin polypeptide is a fusion protein.

10. The method of claim 9 , wherein the fusion protein comprises a reporter polypeptide.

11. The method of claim 9 , wherein the fusion protein comprises a myc epitope.

Assignments (3)
CONFIRMATORY LICENSE Recorded Dec 27, 2010
From: UNIVERSITY OF WASHINGTON, CENTER FOR COMMERCIALIZATION
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 025568/0575 →
CONFIRMATORY LICENSE Recorded Feb 24, 2010
From: UNIVERSITY OF WASHINGTON
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 023982/0854 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 15, 2004
From: MUCHOWSKI, PAUL J.
To: UNIVERSITY OF WASHINGTON
Reel/Frame 015458/0352 →
Continuity (1)
Related Publication 20060084072A1 · Apr 20, 2006