Structure of a Signaling Cannabinoid Receptor 1-G Protein Complex

被引:309
作者
Kumar, Kaavya Krishna [1 ]
Shalev-Benami, Moran [1 ,2 ]
Robertson, Michael J. [1 ,2 ]
Hu, Hongli [1 ,2 ]
Banister, Samuel D. [3 ]
Hollingsworth, Scott A. [1 ,4 ,5 ]
Latorraca, Naomi R. [1 ,4 ,5 ]
Kato, Hideaki E. [1 ]
Hilger, Daniel [1 ]
Maeda, Shoji [1 ]
Weis, William I. [2 ,6 ]
Farrens, David L. [7 ,8 ]
Dror, Ron O. [1 ,4 ,5 ]
Malhotra, Sanjay V. [3 ]
Kobilka, Brian K. [1 ]
Skiniotis, Georgios [1 ,2 ,6 ]
机构
[1] Stanford Univ, Sch Med, Dept Mol & Cellular Physiol, 279 Campus Dr, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Biol Struct, Sch Med, 279 Campus Dr, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Dept Radiat Oncol, Div Radiat & Canc Biol, Stanford, CA 94304 USA
[4] Stanford Univ, Dept Comp Sci, Stanford, CA 94305 USA
[5] Stanford Univ, Biophys Program, Stanford, CA 94305 USA
[6] Stanford Univ, SLAC Natl Accelerator Lab, Dept Photon Sci, Menlo Pk, CA 94025 USA
[7] Oregon Hlth & Sci Univ, Dept Biochem, Portland, OR 97201 USA
[8] Oregon Hlth & Sci Univ, Dept Mol Biol, Portland, OR 97201 USA
基金
澳大利亚国家健康与医学研究理事会;
关键词
MOLECULAR-DYNAMICS; FORCE-FIELD; CRYSTAL-STRUCTURE; CB1; SYSTEM; G(S); VISUALIZATION; VALIDATION; AUTOMATION; ENERGETICS;
D O I
10.1016/j.cell.2018.11.040
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cannabis elicits its mood-enhancing and analgesic effects through the cannabinoid receptor 1 (CB1), a G protein-coupled receptor (GPCR) that signals primarily through the adenylyl cyclase-inhibiting heterotrimeric G protein G(i). Activation of CB1-G(i) signaling pathways holds potential for treating a number of neurological disorders and is thus crucial to understand the mechanism of G(i) activation by CB1. Here, we present the structure of the CB1-G(i) signaling complex bound to the highly potent agonist MDMB-Fubinaca (FUB), a recently emerged illicit synthetic cannabinoid infused in street drugs that have been associated with numerous overdoses and fatalities. The structure illustrates how FUB stabilizes the receptor in an active state to facilitate nucleotide exchange in G(i). The results compose the structural framework to explain CB1 activation by different classes of ligands and provide insights into the G protein coupling and selectivity mechanisms adopted by the receptor.
引用
收藏
页码:448 / +
页数:23
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