Mutagenesis computer experiments in pentameric ligand-gated ion channels: the role of simulation tools with different resolution

被引:11
作者
Crnjar, Alessandro [1 ]
Comitani, Federico [2 ]
Melis, Claudio [3 ]
Molteni, Carla [1 ]
机构
[1] Kings Coll London, Dept Phys, London WC2R 2LS, England
[2] Hosp Sick Children, Program Genet & Genome Biol, Toronto, ON, Canada
[3] Univ Cagliari, Complesso Univ Monserrato, Dipartimento Fis, SP Monserrato Sestu Km 0,700, I-09042 Monserrato, CA, Italy
基金
英国工程与自然科学研究理事会;
关键词
pentameric ligand-gated ion channels; mutagenesis electrophysiology experiments; first principles methods; molecular dynamics; enhanced sampling methods; metadynamics; NICOTINIC ACETYLCHOLINE-RECEPTOR; MOLECULAR-DYNAMICS SIMULATIONS; CATION-PI INTERACTIONS; X-RAY STRUCTURES; CRYSTAL-STRUCTURE; GATING MECHANISM; STRUCTURAL BASIS; BINDING DOMAIN; 5-HT3; RECEPTOR; STRING METHOD;
D O I
10.1098/rsfs.2018.0067
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
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页数:13
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