Felce James H, James John R, Davis Simon J
Kennedy Institute of Rheumatology, University of Oxford, Roosevelt Drive, Oxford, OX3 7FY, UK.
Warwick Medical School, University of Warwick, Coventry, CV4 7AL, UK.
Methods Mol Biol. 2019;1947:183-197. doi: 10.1007/978-1-4939-9121-1_10.
How G protein-coupled receptors are assembled is a matter of considerable interest owing in large part to their remarkable pharmacological importance. For determining receptor stoichiometry, resonance energy transfer-based methods offer considerable advantages insofar as they provide the necessary spatial resolution, and because measurements can be made in situ, relatively easily. This chapter describes three complementary stoichiometric assays that rely on measurements of bioluminescence resonance energy transfer. These quantitative approaches make it possible to identify true protein-protein interactions from non-specific associations that inevitably result from constraining proteins in cellular membranes. In our experience, concordant data obtained in two or more of these assays, benchmarked with suitable controls, strongly predict receptor stoichiometry.
G蛋白偶联受体如何组装是一个备受关注的问题,这在很大程度上归因于它们显著的药理学重要性。对于确定受体化学计量,基于共振能量转移的方法具有相当大的优势,因为它们提供了必要的空间分辨率,并且由于可以在原位相对容易地进行测量。本章描述了三种基于生物发光共振能量转移测量的互补化学计量分析方法。这些定量方法使得从细胞膜中蛋白质受限不可避免产生的非特异性结合中识别真正的蛋白质-蛋白质相互作用成为可能。根据我们的经验,在两种或更多种这些分析中获得的一致数据,并以适当的对照为基准,能有力地预测受体化学计量。