Vilardaga Jean-Pierre, Romero Guillermo, Feinstein Timothy N, Wehbi Vanessa L
Laboratory for GPCR Biology, Department of Pharmacology and Chemical Biology, University of Pittsburgh, School of Medicine, Pittsburgh, Pennsylvania, USA.
Methods Enzymol. 2013;522:337-63. doi: 10.1016/B978-0-12-407865-9.00016-9.
We describe optical and microscopy methods based on Förster resonance energy transfer, fluorescence recovery after photobleaching, and imaging cross-correlation spectroscopy that permit to determine kinetic and dynamic properties of key reactions involved G protein-coupled receptor (GPCR) signaling from the initial ligand binding step to the generation of the second messenger, cAMP. Well suited to determine rate-limiting reactions taking place along a GPCR signaling cascade in live cells, these techniques have also uncovered new concepts in GPCR signaling as well as many interesting mechanistic subtleties by which GPCRs transmit neurotransmitter and hormone signals into cells.
我们描述了基于Förster共振能量转移、光漂白后荧光恢复和成像互相关光谱的光学和显微镜方法,这些方法能够确定参与G蛋白偶联受体(GPCR)信号传导的关键反应的动力学和动态特性,该信号传导从初始配体结合步骤到第二信使cAMP的生成。这些技术非常适合确定活细胞中沿GPCR信号级联发生的限速反应,它们还揭示了GPCR信号传导中的新概念以及许多有趣的机制细节,通过这些细节GPCR将神经递质和激素信号传递到细胞中。