Structures of the M1 and M2 muscarinic acetylcholine receptor/G-protein complexes

被引:237
作者
Maeda, Shoji [1 ]
Qu, Qianhui [1 ,2 ]
Robertson, Michael J. [1 ,2 ]
Skiniotis, Georgios [1 ,2 ]
Kobilka, Brian K. [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Mol & Cellular Physiol, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Struct Biol, Stanford, CA 94305 USA
关键词
CRYO-EM STRUCTURE; AMINO-ACID; ALLOSTERIC MODULATION; CRYSTAL-STRUCTURE; ACTIVATION; SPECIFICITY; SELECTIVITY; REGION; IDENTIFICATION; VISUALIZATION;
D O I
10.1126/science.aaw5188
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Muscarinic acetylcholine receptors are G protein-coupled receptors that respond to acetylcholine and play important signaling roles in the nervous system. There are five muscarinic receptor subtypes (M1R to M5R), which, despite sharing a high degree of sequence identity in the transmembrane region, couple to different heterotrimeric GTP-binding proteins (G proteins) to transmit signals. M1R, M3R, and M5R couple to the G(q/11) family, whereas M2R and M4R couple to the G(i/o) family. Here, we present and compare the cryo-electron microscopy structures of M1R in complex with G(11) and M2R in complex with G(oA). The M1R-G(11) complex exhibits distinct features, including an extended transmembrane helix 5 and carboxyl-terminal receptor tail that interacts with G protein. Detailed analysis of these structures provides a framework for understanding the molecular determinants of G-protein coupling selectivity.
引用
收藏
页码:552 / +
页数:42
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