Hot spots for GPCR signaling: lessons from single-molecule microscopy

被引:15
|
作者
Calebiro, Davide [1 ,2 ,3 ,4 ,5 ]
Jobin, Marie-Lise [4 ,5 ]
机构
[1] Univ Birmingham, Inst Metab & Syst Res, Birmingham, W Midlands, England
[2] Univ Birmingham, Ctr Membrane Prot & Receptors COMPARE, Birmingham, W Midlands, England
[3] Univ Nottingham, Nottingham, England
[4] Univ Wurzburg, Inst Pharmacol, Wurzburg, Germany
[5] Univ Wurzburg, Bioimaging Ctr, Wurzburg, Germany
关键词
CRYO-EM STRUCTURE; BETA(2)-ADRENERGIC RECEPTOR; ADENYLATE-CYCLASE; CRYSTAL-STRUCTURE; ADRENERGIC-RECEPTOR; DYNAMIC PROCESS; PROTEIN; COMPLEX; ARRESTIN; DOMAIN;
D O I
10.1016/j.ceb.2018.11.003
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
G protein-coupled receptors (GPCRs) are among the best-studied membrane receptors, mainly due to their central role in human physiology, involvement in disease and relevance as drug targets. Although biochemical and pharmacological studies have characterized the main steps in GPCR signaling, how GPCRs produce highly specific responses in our cells remains insufficiently understood. New developments in single-molecule microscopy have made it possible to study the protein-protein interactions at the basis of GPCR signaling in previously inconceivable detail. Using this approach, it was recently possible to follow individual receptors and G proteins as they diffuse, interact and signal on the surface of living cells. This has revealed hot spots on the plasma membrane, where receptors and G proteins undergo transient interactions to produce rapid and local signals. Overall, these recent findings reveal a high degree of dynamicity and complexity in signaling by GPCRs, which provides a new basis to understand how these important receptors produce specific effects and might pave the way to innovative pharmacological approaches.
引用
收藏
页码:57 / 63
页数:7
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