Literature DB >> 29665428

Enhanced sampling of glutamate receptor ligand-binding domains.

Albert Y Lau1.   

Abstract

The majority of excitatory synaptic transmission in the central nervous system is mediated by ionotropic glutamate receptors (iGluRs). These membrane-bound protein assemblies consist of modular domains that can be genetically isolated and expressed, which has resulted in a plethora of crystal structures of individual domains in different conformations bound to different ligands. These structures have presented opportunities for molecular dynamics (MD) simulation studies. To examine the free energies that govern molecular behavior, simulation strategies and algorithms have been developed, collectively called enhanced sampling methods This review focuses on the use of enhanced sampling MD simulations of isolated iGluR ligand-binding domains to characterize thermodynamic properties important to receptor function.
Copyright © 2018 Elsevier B.V. All rights reserved.

Keywords:  Conformational change; Enhanced sampling methods; Free energy computations; Glutamate receptors; Ligand binding; Molecular dynamics simulations

Mesh:

Substances:

Year:  2018        PMID: 29665428     DOI: 10.1016/j.neulet.2018.04.018

Source DB:  PubMed          Journal:  Neurosci Lett        ISSN: 0304-3940            Impact factor:   3.046


  2 in total

1.  D-Serine Potently Drives Ligand-Binding Domain Closure in the Ionotropic Glutamate Receptor GluD2.

Authors:  Alfred C Chin; Remy A Yovanno; Tyler J Wied; Ariel Gershman; Albert Y Lau
Journal:  Structure       Date:  2020-07-30       Impact factor: 5.006

Review 2.  Protein dynamics developments for the large scale and cryoEM: case study of ProDy 2.0.

Authors:  James Michael Krieger; Carlos Oscar S Sorzano; Jose Maria Carazo; Ivet Bahar
Journal:  Acta Crystallogr D Struct Biol       Date:  2022-03-16       Impact factor: 7.652

  2 in total

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