IP Library Granted Patent US 8,076,318
Granted Patent B2
US 8,076,318 · App. 10/532,009 · Granted Dec 13, 2011

Caged ligands and uses thereof

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 8,076,318
App. No.
10/532,009
Granted
Dec 13, 2011
Kind
B2
Abstract

Provided are caged compounds comprising a ligand that specifically reacts with a receptor not naturally present in mammals. The cage is released from the ligand upon illumination of the compound with light. Also provided are cells transfected with a gene of interest and a gene encoding a receptor, the gene of interest operably linked to a genetic element capable of being induced by the receptor when bound to a ligand, and the receptor not naturally present in the species of the cell. The cells also comprise a caged ligand of the receptor. Additionally provided are methods of inducing a gene of interest in the above cells. Also provided are methods of repressing a gene of interest in a cell using caged ligands of receptors. Methods are additionally provided for inducing elimination of a target sequence in a cell of a species, using a caged ligand and a recombinase.

Claims (9)

1. A compound comprising a ecdysteroid ligand that specifically reacts with an ecdysone receptor and a molecular cage covalently bound to the ecdysteroid ligand that prevents reaction of the ecdysteroid ligand with the ecdysone receptor, wherein the ecdysteroid ligand is released from the cage and capable of reacting with the ecdysone receptor upon exposure of the compound to light and wherein the molecular cage comprises a nitromethoxybenzyl moiety.

2. The compound of claim 1 , wherein the ligand is an inhibitor of the receptor.

3. The compound of claim 1 , wherein the ligand is selected from the group consisting of ecdysone, 20-hydroxyecdysone, ponasterone A, muristerone A, and inokosterone.

4. The compound of claim 1 , wherein the nitromethoxybenzyl moiety is 1-methyl-4,5-dimethoxy-2-nitrobenzene.

5. The compound of claim 4 , wherein the compound is

6. The compound of claim 1 , wherein the molecular cage is a two-photon cage.

7. The compound of claim 1 , wherein the light comprises wavelengths at 300-400 nm.

8. The compound of claim 1 , wherein the light comprises wavelengths at 325-375 nm.

9. The compound of claim 4 , wherein the compound is

Assignments (3)
CHANGE OF NAME Recorded Oct 19, 2015
From: COM AFFILIATION, INC.
To: ALBERT EINSTEIN COLLEGE OF MEDICINE, INC.
Reel/Frame 036887/0386 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 14, 2015
From: ALBERT EINSTEIN COLLEGE OF MEDICINE OF YESHIVA UNIVERSITY
To: COM AFFILIATION, INC.
Reel/Frame 036865/0901 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 12, 2005
From: LAWRENCE, DAVID S.; PESTELL, RICHARD G.; ALBANESE, CHRISTOPHER
To: ALBERT EINSTEIN COLLEGE OF MEDICINE OF YESHIVA UNIVERSITY
Reel/Frame 016523/0068 →