Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
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
_version_ 1783546710935470080
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
work_keys_str_mv AT blackkatrinaa aconstrictedopeninginkirchannelsdoesnotimpedepotassiumconduction
AT hesitong aconstrictedopeninginkirchannelsdoesnotimpedepotassiumconduction
AT jinruitao aconstrictedopeninginkirchannelsdoesnotimpedepotassiumconduction
AT millerdavidm aconstrictedopeninginkirchannelsdoesnotimpedepotassiumconduction
AT bollajanir aconstrictedopeninginkirchannelsdoesnotimpedepotassiumconduction
AT clarkeoliverb aconstrictedopeninginkirchannelsdoesnotimpedepotassiumconduction
AT johnsonpaul aconstrictedopeninginkirchannelsdoesnotimpedepotassiumconduction
AT windleymonique aconstrictedopeninginkirchannelsdoesnotimpedepotassiumconduction
AT burnschristopherj aconstrictedopeninginkirchannelsdoesnotimpedepotassiumconduction
AT hilladamp aconstrictedopeninginkirchannelsdoesnotimpedepotassiumconduction
AT laverderek aconstrictedopeninginkirchannelsdoesnotimpedepotassiumconduction
AT robinsoncarolv aconstrictedopeninginkirchannelsdoesnotimpedepotassiumconduction
AT smithbrianj aconstrictedopeninginkirchannelsdoesnotimpedepotassiumconduction
AT gulbisjacquelinem aconstrictedopeninginkirchannelsdoesnotimpedepotassiumconduction
AT blackkatrinaa constrictedopeninginkirchannelsdoesnotimpedepotassiumconduction
AT hesitong constrictedopeninginkirchannelsdoesnotimpedepotassiumconduction
AT jinruitao constrictedopeninginkirchannelsdoesnotimpedepotassiumconduction
AT millerdavidm constrictedopeninginkirchannelsdoesnotimpedepotassiumconduction
AT bollajanir constrictedopeninginkirchannelsdoesnotimpedepotassiumconduction
AT clarkeoliverb constrictedopeninginkirchannelsdoesnotimpedepotassiumconduction
AT johnsonpaul constrictedopeninginkirchannelsdoesnotimpedepotassiumconduction
AT windleymonique constrictedopeninginkirchannelsdoesnotimpedepotassiumconduction
AT burnschristopherj constrictedopeninginkirchannelsdoesnotimpedepotassiumconduction
AT hilladamp constrictedopeninginkirchannelsdoesnotimpedepotassiumconduction
AT laverderek constrictedopeninginkirchannelsdoesnotimpedepotassiumconduction
AT robinsoncarolv constrictedopeninginkirchannelsdoesnotimpedepotassiumconduction
AT smithbrianj constrictedopeninginkirchannelsdoesnotimpedepotassiumconduction
AT gulbisjacquelinem constrictedopeninginkirchannelsdoesnotimpedepotassiumconduction