Mafi Amirhossein, Kim Soo-Kyung, Goddard William A
Materials and Process Simulation Center (139-74), California Institute of Technology, Pasadena, CA 91125, USA.
QRB Discov. 2021 Aug 5;2:e9. doi: 10.1017/qrd.2021.7. eCollection 2021.
We report the G protein-first mechanism for activation of G protein-coupled receptors (GPCR) for the three closest subtypes of the opioid receptors (OR), μOR, κOR and δOR. We find that they couple to the inactive Gi protein-bound guanosine diphosphate (GDP) to agonist binding. The inactive Gi protein forms anchors to the intracellular loops of the apo-μOR, apo-κOR and apo-δOR, inducing opening of the cytoplasmic region to form a pre-activated state that holds Gi protein in place until agonist binds. Then, agonist binds to μOR, κOR and δOR already complexed with Gi protein, to trigger the Gαi to open up the tightly coupled GDP binding site, making GDP accessible for GTP exchange, an essential step for Gi signalling. We show that the agonist alone open the intracellular region of μOR and κOR, requiring Gi protein to open the cytoplasmic region by itself. We consider that this G protein-first mechanism may apply to activation of other Class A GPCRs. However, for δOR, agonist binding can open up the intracellular region to encourage Gi protein recruitment. Thus, activation of Gi protein mediated by δOR favourably may proceed with either ligand-first or G protein-first activation mechanisms.
我们报道了阿片受体(OR)的三种最接近亚型,即μ阿片受体(μOR)、κ阿片受体(κOR)和δ阿片受体(δOR)的G蛋白优先激活机制。我们发现,它们在激动剂结合时与结合有鸟苷二磷酸(GDP)的无活性Gi蛋白偶联。无活性的Gi蛋白与脱辅基μOR、脱辅基κOR和脱辅基δOR的细胞内环形成锚定,诱导细胞质区域开放,形成一种预激活状态,使Gi蛋白保持在原位,直到激动剂结合。然后,激动剂与已经与Gi蛋白复合的μOR、κOR和δOR结合,触发Gαi打开紧密偶联的GDP结合位点,使GDP可用于GTP交换,这是Gi信号传导的关键步骤。我们表明,单独的激动剂可打开μOR和κOR的细胞内区域,而需要Gi蛋白自行打开细胞质区域。我们认为这种G蛋白优先机制可能适用于其他A类G蛋白偶联受体(GPCR)的激活。然而,对于δOR,激动剂结合可打开细胞内区域以促进Gi蛋白募集。因此,由δOR介导的Gi蛋白激活可能有利地通过配体优先或G蛋白优先激活机制进行。