CSIR-National Chemical Laboratory , Dr. Homi Bhabha Road , Pune 411 008 , India.
Academy of Scientific and Innovative Research , Sector 19 , Kamla Nehru Nagar , Ghaziabad 201 002 , India.
J Phys Chem B. 2018 Jun 7;122(22):5727-5737. doi: 10.1021/acs.jpcb.8b01657. Epub 2018 May 6.
Gprotein-coupled receptors (GPCRs) are seven transmembrane receptors that mediate a large number of cellular responses and are important drug targets. One of the current challenges in GPCR biology is to analyze the molecular signatures of receptor-lipid interactions and their subsequent effects on GPCR structure, organization, and function. Molecular dynamics simulation studies have been successful in predicting molecular determinants of receptor-lipid interactions. In particular, predicted cholesterol interaction sites appear to correspond well with experimentally determined binding sites and estimated time scales of association. In spite of several success stories, the methodologies in molecular dynamics simulations are still emerging. In this Feature Article, we provide a comprehensive overview of coarse-grain and atomistic molecular dynamics simulations of GPCR-lipid interaction in the context of experimental observations. In addition, we discuss the effect of secondary and tertiary structural constraints in coarse-grain simulations in the context of functional dynamics and structural plasticity of GPCRs. We envision that this comprehensive overview will help resolve differences in computational studies and provide a way forward.
G 蛋白偶联受体(GPCRs)是一种七次跨膜受体,介导大量细胞反应,是重要的药物靶点。目前 GPCR 生物学的挑战之一是分析受体-脂质相互作用的分子特征及其对 GPCR 结构、组织和功能的后续影响。分子动力学模拟研究成功地预测了受体-脂质相互作用的分子决定因素。特别是,预测的胆固醇相互作用位点似乎与实验确定的结合位点和估计的缔合时间尺度很好地对应。尽管有几个成功的案例,但分子动力学模拟的方法仍在不断发展。在这篇专题文章中,我们提供了一个全面的综述,讨论了在实验观察的背景下,粗粒和原子分子动力学模拟 GPCR-脂质相互作用。此外,我们还讨论了在 GPCR 功能动力学和结构可塑性的背景下,粗粒模拟中二级和三级结构约束的影响。我们设想,这个全面的综述将有助于解决计算研究中的差异,并提供前进的方向。