G蛋白偶联受体
受体
视紫红质样受体
异源的
大麻素受体
生物
大麻素
异源表达
G蛋白
细胞生物学
药物发现
C级GPCR
兴奋剂
化学
生物化学
基因
重组DNA
代谢受体
作者
Chanjuan Xu,Yiwei Zhou,Yuxuan Liu,Li Lin,Peng Liu,Xiaomei Wang,Zhengyuan Xu,Jean‐Philippe Pin,Philippe Rondard,Jianfeng Liu
标识
DOI:10.1038/s41467-024-46177-z
摘要
Abstract G protein-coupled receptors (GPCRs) constitute the largest family of membrane proteins and are important drug targets. The discovery of drugs targeting these receptors and their G protein signaling properties are based on assays mainly performed with modified receptors expressed in heterologous cells. However, GPCR responses may differ in their native environment. Here, by using highly sensitive G i/o sensors, we reveal specific properties of G i/o protein-mediated responses triggered by GABA B , α 2 adrenergic and cannabinoid CB1 receptors in primary neurons, different from those in heterologous cells. These include different profiles in the G i/o protein subtypes-mediated responses, and differences in the potencies of some ligands even at similar receptor expression levels. Altogether, our results show the importance of using biosensors compatible with primary cells for evaluating the activities of endogenous GPCRs in their native environment.
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