Pathways and Barriers for Ion Translocation through the 5-HT3A Receptor Channel.

Pentameric ligand gated ion channels (pLGICs) are ionotropic receptors that mediate fast intercellular communications at synaptic level and include either cation selective (e.g., nAChR and 5-HT3) or anion selective (e.g., GlyR, GABAA and GluCl) membrane channels. Among others, 5-HT3 is one of the mo...

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Main Authors: Danilo Di Maio, Balasubramanian Chandramouli, Giuseppe Brancato
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4605793?pdf=render
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spelling doaj-ed944f2797754fcabc7bc84ae7b6221d2020-11-25T01:22:08ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-011010e014025810.1371/journal.pone.0140258Pathways and Barriers for Ion Translocation through the 5-HT3A Receptor Channel.Danilo Di MaioBalasubramanian ChandramouliGiuseppe BrancatoPentameric ligand gated ion channels (pLGICs) are ionotropic receptors that mediate fast intercellular communications at synaptic level and include either cation selective (e.g., nAChR and 5-HT3) or anion selective (e.g., GlyR, GABAA and GluCl) membrane channels. Among others, 5-HT3 is one of the most studied members, since its first cloning back in 1991, and a large number of studies have successfully pinpointed protein residues critical for its activation and channel gating. In addition, 5-HT3 is also the target of a few pharmacological treatments due to the demonstrated benefits of its modulation in clinical trials. Nonetheless, a detailed molecular analysis of important protein features, such as the origin of its ion selectivity and the rather low conductance as compared to other channel homologues, has been unfeasible until the recent crystallization of the mouse 5-HT3A receptor. Here, we present extended molecular dynamics simulations and free energy calculations of the whole 5-HT3A protein with the aim of better understanding its ion transport properties, such as the pathways for ion permeation into the receptor body and the complex nature of the selectivity filter. Our investigation unravels previously unpredicted structural features of the 5-HT3A receptor, such as the existence of alternative intersubunit pathways for ion translocation at the interface between the extracellular and the transmembrane domains, in addition to the one along the channel main axis. Moreover, our study offers a molecular interpretation of the role played by an arginine triplet located in the intracellular domain on determining the characteristic low conductance of the 5-HT3A receptor, as evidenced in previous experiments. In view of these results, possible implications on other members of the superfamily are suggested.http://europepmc.org/articles/PMC4605793?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Danilo Di Maio
Balasubramanian Chandramouli
Giuseppe Brancato
spellingShingle Danilo Di Maio
Balasubramanian Chandramouli
Giuseppe Brancato
Pathways and Barriers for Ion Translocation through the 5-HT3A Receptor Channel.
PLoS ONE
author_facet Danilo Di Maio
Balasubramanian Chandramouli
Giuseppe Brancato
author_sort Danilo Di Maio
title Pathways and Barriers for Ion Translocation through the 5-HT3A Receptor Channel.
title_short Pathways and Barriers for Ion Translocation through the 5-HT3A Receptor Channel.
title_full Pathways and Barriers for Ion Translocation through the 5-HT3A Receptor Channel.
title_fullStr Pathways and Barriers for Ion Translocation through the 5-HT3A Receptor Channel.
title_full_unstemmed Pathways and Barriers for Ion Translocation through the 5-HT3A Receptor Channel.
title_sort pathways and barriers for ion translocation through the 5-ht3a receptor channel.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description Pentameric ligand gated ion channels (pLGICs) are ionotropic receptors that mediate fast intercellular communications at synaptic level and include either cation selective (e.g., nAChR and 5-HT3) or anion selective (e.g., GlyR, GABAA and GluCl) membrane channels. Among others, 5-HT3 is one of the most studied members, since its first cloning back in 1991, and a large number of studies have successfully pinpointed protein residues critical for its activation and channel gating. In addition, 5-HT3 is also the target of a few pharmacological treatments due to the demonstrated benefits of its modulation in clinical trials. Nonetheless, a detailed molecular analysis of important protein features, such as the origin of its ion selectivity and the rather low conductance as compared to other channel homologues, has been unfeasible until the recent crystallization of the mouse 5-HT3A receptor. Here, we present extended molecular dynamics simulations and free energy calculations of the whole 5-HT3A protein with the aim of better understanding its ion transport properties, such as the pathways for ion permeation into the receptor body and the complex nature of the selectivity filter. Our investigation unravels previously unpredicted structural features of the 5-HT3A receptor, such as the existence of alternative intersubunit pathways for ion translocation at the interface between the extracellular and the transmembrane domains, in addition to the one along the channel main axis. Moreover, our study offers a molecular interpretation of the role played by an arginine triplet located in the intracellular domain on determining the characteristic low conductance of the 5-HT3A receptor, as evidenced in previous experiments. In view of these results, possible implications on other members of the superfamily are suggested.
url http://europepmc.org/articles/PMC4605793?pdf=render
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