US2003013137A1PendingUtilityA1

Automated methods of detecting receptor activity

Priority: Mar 13, 2001Filed: Mar 12, 2002Published: Jan 16, 2003
Est. expiryMar 13, 2021(expired)· nominal 20-yr term from priority
G01N 33/5076C12N 2503/00G01N 2333/726C12N 15/1089G01N 2500/10G01N 33/566G01N 2500/04
39
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Claims

Abstract

Methods of detecting G protein-coupled receptor (GPCR) activity in vitro and in vivo are provided. In one embodiment, the method includes providing at least one cell that expresses a GPCR and a plurality of conjugated proteins. Each of the plurality of conjugated proteins is formed by conjugating an arrestin protein and a detectable molecule. The plurality of conjugated proteins are substantially evenly distributed in the cytoplasm of the at least one cell. A first image of the at least one cell is obtained by detecting an amount of energy emitted from the detectable molecules and storing a value relative to the amount of energy. The at least one cell is treated with an agonist. A second image of the at least one cell is obtained. The first image and the second image are compared to detect the localization of at least some of the plurality of conjugated proteins at endocytic vesicles and/or endosomes.

Claims

exact text as granted — not AI-modified
What is claimed is:  
     
         1 . A method of detecting G protein-coupled receptor (GPCR) pathway activity, comprising: 
 providing at least one cell that expresses a GPCR and a plurality of conjugated proteins, each of the plurality of conjugated proteins formed by conjugating an arrestin protein and a detectable molecule, the plurality of conjugated proteins being substantially evenly distributed in the cytoplasm of the at least one cell;    obtaining a first image of the at least one cell by detecting an amount of energy emitted from the detectable molecules and storing a value relative to the amount of energy;    treating the at least one cell with a test compound;    obtaining a second image of the at least one cell by detecting an amount of energy emitted from the detectable molecules and storing a value relative to the amount of energy; and    comparing the first image and the second image to detect the localization of at least some of the plurality of conjugated proteins at at least one of endocytic vesicles and endosomes.    
     
     
         2 . The method of  claim 1 , wherein the step of obtaining a second image of the at least one cell includes setting a threshold intensity such that the energy emitted from detectable molecules evenly distributed in the cytoplasm are excluded.  
     
     
         3 . The method of  claim 2 , wherein the threshold intensity is set to exclude as much as possible of the energy emitted from the detectable molecules that are evenly distributed in the cytoplasm and as little as possible of the energy emitted from the detectable molecules in endocytic vesicles.  
     
     
         4 . The method of  claim 2 , wherein the threshold intensity is set at the mean intensity of all energy emitted in a control cell plus two standard deviations.  
     
     
         5 . The method of  claim 2 , wherein the threshold intensity is set at the mean intensity of all energy emitted in a control cell plus three standard deviations.  
     
     
         6 . The method of  claim 1 , wherein the test compound is a potential agonist or a potential antagonist.  
     
     
         7 . A method of detecting G protein-coupled receptor (GPCR) pathway activity, comprising: 
 providing at least one cell that expresses a GPCR and a plurality of conjugated proteins, each of the plurality of conjugated proteins formed by conjugating an arrestin protein and a detectable molecule, the plurality of conjugated proteins being substantially evenly distributed in the cytoplasm of the at least one cell;    obtaining a first digital image of the at least one cell by detecting and measuring energy emitted from the detectable molecules, the first digital image being formed from an array of a plurality of pixels each having respective intensity values, a respective intensity value being based on the intensity of energy emitted from the detectable molecules associated with a pixel's location in the array;    treating the at least one cell with a test compound;    obtaining a second digital image of the at least one cell by detecting and measuring energy emitted from the detectable molecules, the second digital image being formed from an array of a plurality of pixels each having respective intensity values, a respective intensity value being based on the intensity of energy emitted from the detectable molecules associated with a pixel's location in the array; and    comparing the first digital image and the second digital image to detect the localization of at least some of the plurality of conjugated proteins at at least one of endocytic vesicles and endosomes, the localization of at least some of the plurality of conjugated proteins being detected by a change in apparent intensity of energy emitted from detectable molecules resulting in an increase in the value of at least some of the plurality of pixels.    
     
     
         8 . A method of detecting G protein-coupled receptor (GPCR) pathway activity, comprising: 
 providing at least one cell that expresses a GPCR and a plurality of conjugated proteins, each of the plurality of conjugated proteins formed by conjugating an arrestin protein and a detectable molecule, the plurality of conjugated proteins being substantially evenly distributed in the cytoplasm of the at least one cell;    treating the at least one cell with a test compound;    obtaining a digital image of the at least one cell by detecting and measuring energy emitted from the detectable molecules, the digital image being formed from an array of a plurality of pixels each having respective intensity values, a respective intensity value being based on the intensity of energy emitted from the detectable molecules associated with a pixel's location in the array; and    detecting the localization of at least some of the plurality of conjugated proteins at at least one of endocytic vesicles and endosomes, the localization of at least some of the plurality of conjugated proteins being detected by a change in apparent intensity of energy emitted from detectable molecules resulting at least some of the plurality of pixels having a value above a threshold intensity.    
     
     
         9 . The method of  claim 8 , wherein the step of obtaining a digital image of the at least one cell includes setting the threshold intensity such that the energy emitted from detectable molecules evenly distributed in the cytoplasm are excluded.  
     
     
         10 . The method of  claim 9 , wherein the threshold intensity is set to exclude as much as possible of the energy emitted from the detectable molecules that are evenly distributed in the cytoplasm and as little as possible of the energy emitted from the detectable molecules in endocytic vesicles.  
     
     
         11 . The method of  claim 8 , wherein the threshold intensity is set based on the mean intensity of all energy emitted from detectable molecules in a control cell.  
     
     
         12 . The method of  claim 11 , wherein the threshold intensity is set at the mean intensity of all energy emitted from detectable molecules in a control cell plus two standard deviations.  
     
     
         13 . The method of  claim 11 , wherein the threshold intensity is set at the mean intensity of all energy emitted from detectable molecules in a control cell plus three standard deviations.  
     
     
         14 . The method of  claim 8 , wherein the test compound is a potential agonist or a potential antagonist.  
     
     
         15 . A method of detecting G protein-coupled receptor (GPCR) pathway activity, comprising: 
 providing at least one cell that expresses a GPCR and a plurality of conjugated proteins, each of the plurality of conjugated proteins formed by conjugating an arrestin protein and a detectable molecule, the plurality of conjugated proteins being substantially evenly distributed in the cytoplasm of the at least one cell;    treating the at least one cell with a test compound;    obtaining a digital image of the at least one cell by detecting and measuring energy emitted from the detectable molecules, the digital image being formed from an array of a plurality of pixels each having respective intensity values, a respective intensity value being based on the intensity of energy emitted from the detectable molecules associated with a pixel's location in the array; and    detecting the localization of at least some of the plurality of conjugated proteins by a change in apparent intensity of energy emitted from detectable molecules resulting in at least some of the plurality of pixels having a value above a threshold intensity.    
     
     
         16 . The method of  claim 15 , wherein the step of obtaining a digital image of the at least one cell includes setting the threshold intensity such that the energy emitted from detectable molecules evenly distributed in the cytoplasm are excluded.  
     
     
         17 . The method of  claim 16 , wherein the threshold intensity is set to exclude as much as possible of the energy emitted from the detectable molecules that are evenly distributed in the cytoplasm and as little as possible of the energy emitted from the detectable molecules in endocytic vesicles.  
     
     
         18 . The method of  claim 15 , wherein the threshold intensity is set based on the mean intensity of all energy emitted from detectable molecules in a control cell.  
     
     
         19 . The method of  claim 18 , wherein the threshold intensity is set at the mean intensity of all energy emitted from detectable molecules in a control cell plus two standard deviations.  
     
     
         20 . The method of  claim 18 , wherein the threshold intensity is set at the mean intensity of all energy emitted from detectable molecules in a control cell plus three standard deviations.  
     
     
         21 . The method of  claim 15 , wherein the test compound is a potential agonist or a potential antagonist.

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