Zylbergold Peter, Hébert Terence E
Department of Pharmacology and Therapeutics, McGill University, Montreal, Canada.
Nat Chem Biol. 2009 Sep;5(9):608-9. doi: 10.1038/nchembio0909-608.
The functional architecture of dimeric or oligomeric GPCR signaling remains incompletely understood. Using a clever combination of receptor-G protein fusions and various receptor mutations, new research provides a glimpse into how oligomers might be arranged with respect to the G proteins they interact with.
二聚体或寡聚体G蛋白偶联受体(GPCR)信号传导的功能架构仍未完全被理解。通过巧妙地结合受体 - G蛋白融合以及各种受体突变,新的研究让我们得以一窥寡聚体可能如何相对于它们所相互作用的G蛋白进行排列。