Université Côte d'Azur, CNRS , Institut de Chimie de Nice UMR7272 , 06108 Nice , France.
Department of Brain and Cognitive Sciences , Daegu Gyeongbuk Institute of Science and Technology , Daegu , 711-873 , South Korea.
J Chem Theory Comput. 2018 Aug 14;14(8):4467-4473. doi: 10.1021/acs.jctc.8b00216. Epub 2018 Jul 25.
A replica-exchange protocol remarkably enhances the sampling of the activation dynamics of the neurotensin receptor type 1, a G protein-coupled receptor (GPCR) and important drug target. Our work highlights the dynamic communication between conformational changes of the agonist and the G protein-binding site, via contraction-oscillation of the orthosteric pocket. It also gives insights into the mechanism by which certain mutations diminish or stimulate activation. The replica-exchange protocol effectively enhances barrier crossing where standard brute-force molecular dynamics simulations fail. It is readily applicable to other GPCRs and represents a promising approach for virtual ligand screening, using the typical features of receptor activation as a benchmark.
一个复制交换协议显著提高了神经降压素受体 1 的激活动力学的采样,神经降压素受体 1 是一种 G 蛋白偶联受体 (GPCR),也是一个重要的药物靶点。我们的工作强调了激动剂构象变化与 G 蛋白结合位点之间的动态通讯,通过正构口袋的收缩-振荡来实现。它还深入了解了某些突变如何减少或刺激激活的机制。复制交换协议有效地增强了标准强力分子动力学模拟失败的势垒穿越。它很容易适用于其他 GPCR,并代表了一种有前途的虚拟配体筛选方法,使用受体激活的典型特征作为基准。