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Structural Mechanisms of Gating in Ionotropic Glutamate Receptors

[Image: see text] Ionotropic glutamate receptors (iGluRs) are ligand-gated ion channels that mediate the majority of excitatory neurotransmission in the central nervous system. iGluRs open their ion channels in response to binding of the neurotransmitter glutamate, rapidly depolarize the postsynapti...

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Detalles Bibliográficos
Autores principales: Twomey, Edward C., Sobolevsky, Alexander I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2017
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5780838/
https://www.ncbi.nlm.nih.gov/pubmed/29037031
http://dx.doi.org/10.1021/acs.biochem.7b00891
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author Twomey, Edward C.
Sobolevsky, Alexander I.
author_facet Twomey, Edward C.
Sobolevsky, Alexander I.
author_sort Twomey, Edward C.
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description [Image: see text] Ionotropic glutamate receptors (iGluRs) are ligand-gated ion channels that mediate the majority of excitatory neurotransmission in the central nervous system. iGluRs open their ion channels in response to binding of the neurotransmitter glutamate, rapidly depolarize the postsynaptic neuronal membrane, and initiate signal transduction. Recent studies using X-ray crystallography and cryo-electron microscopy have determined full-length iGluR structures that (1) uncover the receptor architecture in an unliganded, resting state, (2) reveal conformational changes produced by ligands in order to activate iGluRs, open their ion channels, and conduct ions, and (3) show how activated, glutamate-bound iGluRs can adopt a nonconducting desensitized state. These new findings, combined with the results of previous structural and functional experiments, kinetic and molecular modeling, mutagenesis, and biochemical analyses, provide new views on the structural mechanisms of iGluR gating.
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spelling pubmed-57808382018-01-25 Structural Mechanisms of Gating in Ionotropic Glutamate Receptors Twomey, Edward C. Sobolevsky, Alexander I. Biochemistry [Image: see text] Ionotropic glutamate receptors (iGluRs) are ligand-gated ion channels that mediate the majority of excitatory neurotransmission in the central nervous system. iGluRs open their ion channels in response to binding of the neurotransmitter glutamate, rapidly depolarize the postsynaptic neuronal membrane, and initiate signal transduction. Recent studies using X-ray crystallography and cryo-electron microscopy have determined full-length iGluR structures that (1) uncover the receptor architecture in an unliganded, resting state, (2) reveal conformational changes produced by ligands in order to activate iGluRs, open their ion channels, and conduct ions, and (3) show how activated, glutamate-bound iGluRs can adopt a nonconducting desensitized state. These new findings, combined with the results of previous structural and functional experiments, kinetic and molecular modeling, mutagenesis, and biochemical analyses, provide new views on the structural mechanisms of iGluR gating. American Chemical Society 2017-10-16 2018-01-23 /pmc/articles/PMC5780838/ /pubmed/29037031 http://dx.doi.org/10.1021/acs.biochem.7b00891 Text en Copyright © 2017 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Twomey, Edward C.
Sobolevsky, Alexander I.
Structural Mechanisms of Gating in Ionotropic Glutamate Receptors
title Structural Mechanisms of Gating in Ionotropic Glutamate Receptors
title_full Structural Mechanisms of Gating in Ionotropic Glutamate Receptors
title_fullStr Structural Mechanisms of Gating in Ionotropic Glutamate Receptors
title_full_unstemmed Structural Mechanisms of Gating in Ionotropic Glutamate Receptors
title_short Structural Mechanisms of Gating in Ionotropic Glutamate Receptors
title_sort structural mechanisms of gating in ionotropic glutamate receptors
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5780838/
https://www.ncbi.nlm.nih.gov/pubmed/29037031
http://dx.doi.org/10.1021/acs.biochem.7b00891
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