Department of Molecular and Cellular Physiology, Stanford University School of Medicine, 279 Campus Drive, Stanford, CA 94305, USA.
Department of Molecular and Cellular Physiology, Stanford University School of Medicine, 279 Campus Drive, Stanford, CA 94305, USA; Department of Structural Biology, Stanford University School of Medicine, 279 Campus Drive, Stanford, CA 94305, USA.
Cell. 2019 Jan 24;176(3):448-458.e12. doi: 10.1016/j.cell.2018.11.040. Epub 2019 Jan 10.
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. Activation of CB1-G signaling pathways holds potential for treating a number of neurological disorders and is thus crucial to understand the mechanism of G activation by CB1. Here, we present the structure of the CB1-G 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. 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.
大麻通过大麻素受体 1(CB1)发挥其改善情绪和镇痛作用,CB1 是一种 G 蛋白偶联受体(GPCR),主要通过抑制腺苷酸环化酶的异三聚体 G 蛋白 G 传递信号。激活 CB1-G 信号通路有可能治疗多种神经疾病,因此理解 CB1 对 G 的激活机制至关重要。在这里,我们展示了与高活性激动剂 MDMB-Fubinaca(FUB)结合的 CB1-G 信号复合物的结构,FUB 是一种新出现的非法合成大麻素,掺入街头毒品中,与许多过量和死亡事件有关。该结构说明了 FUB 如何稳定受体处于激活状态,以促进 G 中的核苷酸交换。研究结果构成了结构框架,用于解释不同类别的配体对 CB1 的激活作用,并深入了解受体采用的 G 蛋白偶联和选择性机制。