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Molecular basis of ion permeability in a voltage‐gated sodium channel
Voltage‐gated sodium channels are essential for electrical signalling across cell membranes. They exhibit strong selectivities for sodium ions over other cations, enabling the finely tuned cascade of events associated with action potentials. This paper describes the ion permeability characteristics...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4972137/ https://www.ncbi.nlm.nih.gov/pubmed/26873592 http://dx.doi.org/10.15252/embj.201593285 |
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author | Naylor, Claire E Bagnéris, Claire DeCaen, Paul G Sula, Altin Scaglione, Antonella Clapham, David E Wallace, BA |
author_facet | Naylor, Claire E Bagnéris, Claire DeCaen, Paul G Sula, Altin Scaglione, Antonella Clapham, David E Wallace, BA |
author_sort | Naylor, Claire E |
collection | PubMed |
description | Voltage‐gated sodium channels are essential for electrical signalling across cell membranes. They exhibit strong selectivities for sodium ions over other cations, enabling the finely tuned cascade of events associated with action potentials. This paper describes the ion permeability characteristics and the crystal structure of a prokaryotic sodium channel, showing for the first time the detailed locations of sodium ions in the selectivity filter of a sodium channel. Electrostatic calculations based on the structure are consistent with the relative cation permeability ratios (Na(+) ≈ Li(+) ≫ K(+), Ca(2+), Mg(2+)) measured for these channels. In an E178D selectivity filter mutant constructed to have altered ion selectivities, the sodium ion binding site nearest the extracellular side is missing. Unlike potassium ions in potassium channels, the sodium ions in these channels appear to be hydrated and are associated with side chains of the selectivity filter residues, rather than polypeptide backbones. |
format | Online Article Text |
id | pubmed-4972137 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-49721372016-10-06 Molecular basis of ion permeability in a voltage‐gated sodium channel Naylor, Claire E Bagnéris, Claire DeCaen, Paul G Sula, Altin Scaglione, Antonella Clapham, David E Wallace, BA EMBO J Articles Voltage‐gated sodium channels are essential for electrical signalling across cell membranes. They exhibit strong selectivities for sodium ions over other cations, enabling the finely tuned cascade of events associated with action potentials. This paper describes the ion permeability characteristics and the crystal structure of a prokaryotic sodium channel, showing for the first time the detailed locations of sodium ions in the selectivity filter of a sodium channel. Electrostatic calculations based on the structure are consistent with the relative cation permeability ratios (Na(+) ≈ Li(+) ≫ K(+), Ca(2+), Mg(2+)) measured for these channels. In an E178D selectivity filter mutant constructed to have altered ion selectivities, the sodium ion binding site nearest the extracellular side is missing. Unlike potassium ions in potassium channels, the sodium ions in these channels appear to be hydrated and are associated with side chains of the selectivity filter residues, rather than polypeptide backbones. John Wiley and Sons Inc. 2016-02-12 2016-04-15 /pmc/articles/PMC4972137/ /pubmed/26873592 http://dx.doi.org/10.15252/embj.201593285 Text en © 2016 The Authors. Published under the terms of the CC BY 4.0 license This is an open access article under the terms of the Creative Commons Attribution 4.0 (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Naylor, Claire E Bagnéris, Claire DeCaen, Paul G Sula, Altin Scaglione, Antonella Clapham, David E Wallace, BA Molecular basis of ion permeability in a voltage‐gated sodium channel |
title | Molecular basis of ion permeability in a voltage‐gated sodium channel |
title_full | Molecular basis of ion permeability in a voltage‐gated sodium channel |
title_fullStr | Molecular basis of ion permeability in a voltage‐gated sodium channel |
title_full_unstemmed | Molecular basis of ion permeability in a voltage‐gated sodium channel |
title_short | Molecular basis of ion permeability in a voltage‐gated sodium channel |
title_sort | molecular basis of ion permeability in a voltage‐gated sodium channel |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4972137/ https://www.ncbi.nlm.nih.gov/pubmed/26873592 http://dx.doi.org/10.15252/embj.201593285 |
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