| Literature DB >> 36087581 |
Can Cao1, Ximena Barros-Álvarez2, Shicheng Zhang1, Kuglae Kim1, Marc A Dämgen3, Ouliana Panova2, Carl-Mikael Suomivuori3, Jonathan F Fay4, Xiaofang Zhong5, Brian E Krumm1, Ryan H Gumpper1, Alpay B Seven2, Michael J Robertson2, Nevan J Krogan5, Ruth Hüttenhain5, David E Nichols6, Ron O Dror7, Georgios Skiniotis8, Bryan L Roth9.
Abstract
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.Entities:
Keywords: Gq protein; HTR2B; LSD; functional selectivity; psychedelic; signaling transduction; structural biology; β-arrestin-1
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Year: 2022 PMID: 36087581 PMCID: PMC9583076 DOI: 10.1016/j.neuron.2022.08.006
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 18.688