麦角酸二乙酰胺
血清素
受体
5-羟色胺受体
药理学
血清素拮抗剂
神经科学
信号转导
化学
心理学
生物
细胞生物学
生物化学
作者
Can Cao,Ximena Barros-Álvarez,Shicheng Zhang,Kuglae Kim,Marc A. Dämgen,Ouliana Panova,Carl‐Mikael Suomivuori,Jonathan F. Fay,Xiaofang Zhong,B. Krumm,Ryan H. Gumpper,Alpay B. Seven,Michael J. Robertson,Nevan J. Krogan,Ruth Hüttenhain,David E. Nichols,Ron O. Dror,Georgios Skiniotis,Bryan L. Roth
出处
期刊:Neuron
[Cell Press]
日期:2022-09-09
卷期号:110 (19): 3154-3167.e7
被引量:81
标识
DOI:10.1016/j.neuron.2022.08.006
摘要
Serotonin (5-hydroxytryptamine [5-HT]) 5-HT2-family receptors represent essential targets for lysergic acid diethylamide (LSD) and all other psychedelic drugs. Although the primary psychedelic drug effects are mediated by the 5-HT2A serotonin receptor (HTR2A), the 5-HT2B serotonin receptor (HTR2B) has been used as a model receptor to study the activation mechanisms of psychedelic drugs due to its high expression and similarity to HTR2A. In this study, we determined the cryo-EM structures of LSD-bound HTR2B in the transducer-free, Gq-protein-coupled, and β-arrestin-1-coupled states. These structures provide distinct signaling snapshots of LSD’s action, ranging from the transducer-free, partially active state to the transducer-coupled, fully active states. Insights from this study will both provide comprehensive molecular insights into the signaling mechanisms of the prototypical psychedelic LSD and accelerate the discovery of novel psychedelic drugs.
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