Real-time monitoring of receptor and G-protein interactions in living cells

被引:323
作者
Galés, C
Rebois, RV
Hogue, M
Trieu, P
Breit, A
Hébert, TE
Bouvier, M
机构
[1] Univ Montreal, Dept Biochem, Montreal, PQ H3C 3J7, Canada
[2] Natl Inst Hlth, Lab Cellular Biol, Rockville, MD 20850 USA
[3] Univ Montreal, Inst Cardiol Montreal, Montreal, PQ H1T 1C8, Canada
[4] Univ Montreal, Dept Anesthesiol, Montreal, PQ H1T 1C8, Canada
关键词
D O I
10.1038/NMETH743
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
G protein-coupled receptors (GPCRs) represent the largest family of proteins involved in signal transduction. Here we present a bioluminescence resonance energy transfer (BRET) assay that directly monitors in real time the early interactions between human GPCRs and their cognate G-protein subunits in living human cells. In addition to detecting basal precoupling of the receptors to Galpha-, Gbeta- and Ggamma-subunits, BRET measured very rapid ligand-induced increases in the interaction between receptor and Galphabetagamma-complexes (t(1/2) similar to 300 ms) followed by a slower (several minutes) decrease, reflecting receptor desensitization. The agonist-promoted increase in GPCR-Gbetagamma interaction was highly dependent on the identity of the Galpha-subunit present in the complex. Therefore, this G protein-activity biosensor provides a novel toot to directly probe the dynamics and selectivity of receptor-mediated, G-protein activation-deactivation cycles that could be advantageously used to identify ligands for orphan GPCRs.
引用
收藏
页码:177 / 184
页数:8
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