Crnjar Alessandro, Comitani Federico, Melis Claudio, Molteni Carla
King's College London, Department of Physics, Strand, London WC2R 2LS, UK.
Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.
Interface Focus. 2019 Jun 6;9(3):20180067. doi: 10.1098/rsfs.2018.0067. Epub 2019 Apr 19.
Pentameric ligand-gated ion channels (pLGICs) are an important class of widely expressed membrane neuroreceptors, which play a crucial role in fast synaptic communications and are involved in several neurological conditions. They are activated by the binding of neurotransmitters, which trigger the transmission of an electrical signal via facilitated ion flux. They can also be activated, inhibited or modulated by a number of drugs. Mutagenesis electrophysiology experiments, with natural or unnatural amino acids, have provided a large body of functional data that, together with emerging structural information from X-ray spectroscopy and cryo-electron microscopy, are helping unravel the complex working mechanisms of these neuroreceptors. Computer simulations are complementing these mutagenesis experiments, with insights at various levels of accuracy and resolution. Here, we review how a selection of computational tools, including first principles methods, classical molecular dynamics and enhanced sampling techniques, are contributing to construct a picture of how pLGICs function and can be pharmacologically targeted to treat the disorders they are responsible for.
五聚体配体门控离子通道(pLGICs)是一类广泛表达的重要膜神经受体,在快速突触通讯中起关键作用,并与多种神经疾病有关。它们通过神经递质的结合而被激活,神经递质通过促进离子通量触发电信号的传递。它们也可被多种药物激活、抑制或调节。使用天然或非天然氨基酸的诱变电生理学实验提供了大量功能数据,这些数据与X射线光谱学和冷冻电子显微镜的新结构信息一起,有助于揭示这些神经受体的复杂工作机制。计算机模拟正在补充这些诱变实验,提供不同精度和分辨率水平的见解。在这里,我们综述了一系列计算工具,包括第一性原理方法、经典分子动力学和增强采样技术,如何有助于构建pLGICs的功能图景,以及如何从药理学角度靶向治疗由它们引起的疾病。