致幻剂
生物
体内
药物发现
神经科学
受体
血清素
药理学
5-羟色胺受体
滥用药物
药品
计算生物学
生物信息学
生物化学
生物技术
作者
Chunyang Dong,Calvin Ly,Lee E. Dunlap,Maxemiliano V. Vargas,Junqing Sun,In-Wook Hwang,Arya Azinfar,Won Chan Oh,William C. Wetsel,David E. Olson,Lin Tian
出处
期刊:Cell
[Elsevier]
日期:2021-04-28
卷期号:184 (10): 2779-2792.e18
被引量:125
标识
DOI:10.1016/j.cell.2021.03.043
摘要
Ligands can induce G protein-coupled receptors (GPCRs) to adopt a myriad of conformations, many of which play critical roles in determining the activation of specific signaling cascades associated with distinct functional and behavioral consequences. For example, the 5-hydroxytryptamine 2A receptor (5-HT2AR) is the target of classic hallucinogens, atypical antipsychotics, and psychoplastogens. However, currently available methods are inadequate for directly assessing 5-HT2AR conformation both in vitro and in vivo. Here, we developed psychLight, a genetically encoded fluorescent sensor based on the 5-HT2AR structure. PsychLight detects behaviorally relevant serotonin release and correctly predicts the hallucinogenic behavioral effects of structurally similar 5-HT2AR ligands. We further used psychLight to identify a non-hallucinogenic psychedelic analog, which produced rapid-onset and long-lasting antidepressant-like effects after a single administration. The advent of psychLight will enable in vivo detection of serotonin dynamics, early identification of designer drugs of abuse, and the development of 5-HT2AR-dependent non-hallucinogenic therapeutics.
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