Structures of the M1 and M2 muscarinic acetylcholine receptor/G-protein complexes
Author(s) -
Shoji Maeda,
Qianhui Qu,
Michael J. Robertson,
Georgios Skiniotis,
Brian K. Kobilka
Publication year - 2019
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.aaw5188
Subject(s) - muscarinic acetylcholine receptor , g protein coupled receptor , receptor , acetylcholine , acetylcholine receptor , muscarinic acetylcholine receptor m5 , chemistry , g protein , biophysics , muscarinic acetylcholine receptor m2 , muscarinic acetylcholine receptor m3 , microbiology and biotechnology , biochemistry , biology , pharmacology
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.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom