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A constricted opening in Kir channels does not impede potassium conduction
The canonical mechanistic model explaining potassium channel gating is of a conformational change that alternately dilates and constricts a collar-like intracellular entrance to the pore. It is based on the premise that K(+) ions maintain a complete hydration shell while passing between the transmem...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7295778/ https://www.ncbi.nlm.nih.gov/pubmed/32541684 http://dx.doi.org/10.1038/s41467-020-16842-0 |
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author | Black, Katrina A. He, Sitong Jin, Ruitao Miller, David M. Bolla, Jani R. Clarke, Oliver B. Johnson, Paul Windley, Monique Burns, Christopher J. Hill, Adam P. Laver, Derek Robinson, Carol V. Smith, Brian J. Gulbis, Jacqueline M. |
author_facet | Black, Katrina A. He, Sitong Jin, Ruitao Miller, David M. Bolla, Jani R. Clarke, Oliver B. Johnson, Paul Windley, Monique Burns, Christopher J. Hill, Adam P. Laver, Derek Robinson, Carol V. Smith, Brian J. Gulbis, Jacqueline M. |
author_sort | Black, Katrina A. |
collection | PubMed |
description | The canonical mechanistic model explaining potassium channel gating is of a conformational change that alternately dilates and constricts a collar-like intracellular entrance to the pore. It is based on the premise that K(+) ions maintain a complete hydration shell while passing between the transmembrane cavity and cytosol, which must be accommodated. To put the canonical model to the test, we locked the conformation of a Kir K(+) channel to prevent widening of the narrow collar. Unexpectedly, conduction was unimpaired in the locked channels. In parallel, we employed all-atom molecular dynamics to simulate K(+) ions moving along the conduction pathway between the lower cavity and cytosol. During simulations, the constriction did not significantly widen. Instead, transient loss of some water molecules facilitated K(+) permeation through the collar. The low free energy barrier to partial dehydration in the absence of conformational change indicates Kir channels are not gated by the canonical mechanism. |
format | Online Article Text |
id | pubmed-7295778 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-72957782020-06-19 A constricted opening in Kir channels does not impede potassium conduction Black, Katrina A. He, Sitong Jin, Ruitao Miller, David M. Bolla, Jani R. Clarke, Oliver B. Johnson, Paul Windley, Monique Burns, Christopher J. Hill, Adam P. Laver, Derek Robinson, Carol V. Smith, Brian J. Gulbis, Jacqueline M. Nat Commun Article The canonical mechanistic model explaining potassium channel gating is of a conformational change that alternately dilates and constricts a collar-like intracellular entrance to the pore. It is based on the premise that K(+) ions maintain a complete hydration shell while passing between the transmembrane cavity and cytosol, which must be accommodated. To put the canonical model to the test, we locked the conformation of a Kir K(+) channel to prevent widening of the narrow collar. Unexpectedly, conduction was unimpaired in the locked channels. In parallel, we employed all-atom molecular dynamics to simulate K(+) ions moving along the conduction pathway between the lower cavity and cytosol. During simulations, the constriction did not significantly widen. Instead, transient loss of some water molecules facilitated K(+) permeation through the collar. The low free energy barrier to partial dehydration in the absence of conformational change indicates Kir channels are not gated by the canonical mechanism. Nature Publishing Group UK 2020-06-15 /pmc/articles/PMC7295778/ /pubmed/32541684 http://dx.doi.org/10.1038/s41467-020-16842-0 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Black, Katrina A. He, Sitong Jin, Ruitao Miller, David M. Bolla, Jani R. Clarke, Oliver B. Johnson, Paul Windley, Monique Burns, Christopher J. Hill, Adam P. Laver, Derek Robinson, Carol V. Smith, Brian J. Gulbis, Jacqueline M. A constricted opening in Kir channels does not impede potassium conduction |
title | A constricted opening in Kir channels does not impede potassium conduction |
title_full | A constricted opening in Kir channels does not impede potassium conduction |
title_fullStr | A constricted opening in Kir channels does not impede potassium conduction |
title_full_unstemmed | A constricted opening in Kir channels does not impede potassium conduction |
title_short | A constricted opening in Kir channels does not impede potassium conduction |
title_sort | constricted opening in kir channels does not impede potassium conduction |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7295778/ https://www.ncbi.nlm.nih.gov/pubmed/32541684 http://dx.doi.org/10.1038/s41467-020-16842-0 |
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