IP Library Granted Patent US 8,178,496
Granted Patent B2
US 8,178,496 · App. 12/338,880 · Granted May 15, 2012

Photoreactive regulator of glutamate receptor function and methods of use thereof

Assignee: The Regents of the University of California
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Quick Facts
Patent No.
US 8,178,496
App. No.
12/338,880
Granted
May 15, 2012
Kind
B2
Abstract

The present invention provides a synthetic regulator of glutamate receptor function, which regulator is a light-sensitive (photoreactive) regulator. The present invention further provides a light-regulated glutamate receptor that includes a subject synthetic regulator non-covalently associated with the glutamate receptor. Also provided are cells and membranes comprising a subject light-regulated glutamate receptor. The present invention further provides methods of modulating glutamate receptor function, involving use of light. The present invention further provides methods of identifying agents that modulate glutamate receptor function.

Claims (13)

1. A synthetic regulator of glutamate receptor function, the regulator comprising:

a) a photoisomerizable group selected from an azobenzene, a fulgide, a spiropyran, a triphenyl methane, a thioindigo, a diarylethene, and an overcrowded alkene;

b) a ligand that binds to a ligand binding site of said glutamate receptor, wherein the ligand is selected from the group consisting of glutamate, methylglutamate, 4-allyl glutamate, N-methyl-D-aspartate, D-serine, or glycine,

wherein the ligand is covalently linked to the photoisomerizable group, and

wherein the synthetic regulator does not comprise a linker domain comprising a binding moiety that provides for stable association with the glutamate receptor.

2. The synthetic regulator of claim 1 , wherein the photoisomerizable group comprises an azobenzene.

3. The synthetic regulator of claim 1 , wherein photoisomerization of the photoisomerizable group results in a change in the binding of the ligand to the ligand-binding site, thereby regulating the function of said glutamate receptor.

4. The synthetic regulator of claim 1 , wherein the glutamate receptor is an ionotropic glutamate receptor.

5. The synthetic regulator of claim 4 , wherein the ionotropic glutamate receptor is an N-methyl-D-aspartate (NMDA) receptor, an α-amino-3-hydroxy-5-methyl-4-isoxazole-propionate (AMPA) receptor, or a kainate (KA) receptor.

6. The synthetic regulator of claim 1 , wherein the synthetic regulator has the structure:

7. A pharmaceutical composition comprising:

a) the synthetic regulator of claim 1 ; and

b) a pharmaceutically acceptable excipient.

Assignments (3)
CONFIRMATORY LICENSE Recorded Aug 17, 2010
From: REGENTS OF THE UNIVERSITY OF CALIFORNIA, THE
To: ENERGY, UNITED STATE DEPARTMENT OF
Reel/Frame 024849/0954 →
CONFIRMATORY LICENSE Recorded Jul 31, 2009
From: UNIVERSITY OF CALIFORNIA BERKELEY
To: NATIONAL SCIENCE FOUNDATION
Reel/Frame 023036/0739 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 30, 2009
From: TRAUNER, DIRK; ISACOFF, EHUD Y.; VOLGRAF, MATTHEW; GOROSTIZA LANGA, PABLO IGNACIO
To: THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
Reel/Frame 022470/0752 →
Continuity (2)
Provisional Application 61016233 · Dec 21, 2007
Related Publication 20090181454A1 · Jul 16, 2009