CypHer 5: A generic approach for measuring the activation and trafficking of G protein-coupled receptors in live cells

被引:27
作者
Adie, EJ
Francis, MJ
Davies, J
Smith, L
Marenghi, A
Hather, C
Hadingham, K
Michael, NP
Milligan, G
Gamel, S
机构
[1] Amersham Biosci, Bioassays, Dev, Cardiff CF14 7YT, S Glam, Wales
[2] Univ Glasgow, Inst Biomed & Life Sci, Div Biochem & Mol Biol, Mol Pharmacol Grp, Glasgow, Lanark, Scotland
关键词
D O I
10.1089/15406580360545062
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
GPCRs are one of the most popular classes of therapeutic drug targets. It is therefore important to design specific assay formats to readily identify ligands at these receptors. CypHer 5 technology utilizes the general ability of GPCRs to be internalized into the endosomal pathway of a cell in response to agonist ligands. The CypHer 5 dye is fluorescent in acidic environments, but nonfluorescent at neutral pH. When CypHer 5 is bound to a receptor on the extracellular surface of the cell, it is essentially nonfluorescent. On internalization into a cell, it displays a significant increase in fluorescence. Here we demonstrate the detection of agonist activation of two GPCRs in stably transfected live cells using CypHer 5 technology. The G(q)-coupled TRHR-1 and the G(s)-coupled beta(2)-adrenoceptor were both N-terminally tagged with VSV-G. Following addition of CypHer 5-labeled anti-VSV-G antibodies to HEK 293 cells stably expressing the beta(2)-adrenoceptor or CHO-K1 cells stably expressing the TRHR-1, the cells were treated with agonists and then imaged on Amersham Biosciences' IN Cell Analyzer 3000. Data were quantified using a granularity analysis module. Concentration-response curves were obtained with signal-to-background ratios of 7:1 for both receptors. An EC50 of 0.52 nM was observed on TRH stimulation of the TRHR-1, and an EC50 of 30 nM was obtained on isoprenaline stimulation of the beta(2)-adrenoceptor. These results demonstrated that the CypHer technology was capable of measuring high-potency agonist responses. The beta(2)-adrenoceptor antagonist, alprenolol, competed for isoprenaline with an IC50 of 30 nM, indicating that a high-potency antagonist inhibition curve could also be observed using CypHer. CypHer 5 provides a generic tool to measure GPCR activation in a live cell, homogeneous assay format, and may be equally suitable for detecting activation of other classes of cell surface receptors.
引用
收藏
页码:251 / 259
页数:9
相关论文
共 31 条
[1]   A pH-sensitive fluor, CypHer™ 5, used to monitor agonist-induced g protein-coupled receptor internalization in live cells [J].
Adie, EJ ;
Kalinka, S ;
Smith, L ;
Francis, MJ ;
Marenghi, A ;
Cooper, ME ;
Briggs, M ;
Michael, NP ;
Milligan, G ;
Game, S .
BIOTECHNIQUES, 2002, 33 (05) :1152-1157
[2]  
AUTHIER F, 1994, J BIOL CHEM, V269, P3010
[3]   Diversity of G protein-coupled receptor signaling pathways to ERK/MAP kinase [J].
Belcheva, MM ;
Coscia, CJ .
NEUROSIGNALS, 2002, 11 (01) :34-44
[4]  
BRIGGS MS, 2000, J CHEM SOC CHEM COMM, V32, P2323
[5]   Antidepressant-induced switch of β1-adrenoceptor trafficking as a mechanism for drug action [J].
Bürgi, S ;
Baltensperger, K ;
Honegger, UE .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (02) :1044-1052
[6]   The use of biosensors to study GPCR function: Applications for high-content screening [J].
Conway, BR ;
Demarest, KT .
RECEPTORS & CHANNELS, 2002, 8 (5-6) :331-341
[7]   Real time visualization of agonist-mediated redistribution and internalization of a green fluorescent protein-tagged form of the thyrotropin-releasing hormone receptor [J].
Drmota, T ;
Gould, GW ;
Milligan, G .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (37) :24000-24008
[8]   Localization of G-protein-coupled receptors in health and disease [J].
Edwards, SW ;
Tan, CM ;
Limbird, LE .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2000, 21 (08) :304-308
[9]  
Ferguson SSG, 2001, PHARMACOL REV, V53, P1
[10]   From genes to effective drugs for neurological and psychiatric diseases [J].
Hefti, F .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2001, 22 (04) :159-160