Journal article
Structure of the adenosine-bound human adenosine A1 receptor-Gi complex
CJ Draper-Joyce, M Khoshouei, DM Thal, YL Liang, ATN Nguyen, SGB Furness, H Venugopal, JA Baltos, JM Plitzko, R Danev, W Baumeister, LT May, D Wootten, PM Sexton, A Glukhova, A Christopoulos
Nature | NATURE PUBLISHING GROUP | Published : 2018
Abstract
The class A adenosine A1 receptor (A1R) is a G-protein-coupled receptor that preferentially couples to inhibitory Gi/o heterotrimeric G proteins, has been implicated in numerous diseases, yet remains poorly targeted. Here we report the 3.6 Å structure of the human A1R in complex with adenosine and heterotrimeric Gi2 protein determined by Volta phase plate cryo-electron microscopy. Compared to inactive A1R, there is contraction at the extracellular surface in the orthosteric binding site mediated via movement of transmembrane domains 1 and 2. At the intracellular surface, the G protein engages the A1R primarily via amino acids in the C terminus of the Gαi α5-helix, concomitant with a 10.5 Å o..
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Awarded by Monash University
Funding Acknowledgements
This work was supported by the Monash University Ramaciotti Centre for Cryo-Electron Microscopy, National Health and Medical Research Council of Australia (NHMRC) project grant APP1145420 and NHMRC program grant APP1055134. A.C., P.M.S. and D.W. are NHMRC Senior Principal Research, Principal Research and Career Development Fellows, respectively. A.G. and D.M.T. are Australian Research Council Discovery Early Career Research Fellows. L.T.M. is an Australian Heart Foundation Future Leaders Fellow.