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The gating cycle of a K(+) channel at atomic resolution
C-type inactivation in potassium channels helps fine-tune long-term channel activity through conformational changes at the selectivity filter. Here, through the use of cross-linked constitutively open constructs, we determined the structures of KcsA’s mutants that stabilize the selectivity filter in...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5711375/ https://www.ncbi.nlm.nih.gov/pubmed/29165243 http://dx.doi.org/10.7554/eLife.28032 |
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author | Cuello, Luis G Cortes, D Marien Perozo, Eduardo |
author_facet | Cuello, Luis G Cortes, D Marien Perozo, Eduardo |
author_sort | Cuello, Luis G |
collection | PubMed |
description | C-type inactivation in potassium channels helps fine-tune long-term channel activity through conformational changes at the selectivity filter. Here, through the use of cross-linked constitutively open constructs, we determined the structures of KcsA’s mutants that stabilize the selectivity filter in its conductive (E71A, at 2.25 Å) and deep C-type inactivated (Y82A at 2.4 Å) conformations. These structural snapshots represent KcsA’s transient open-conductive (O/O) and the stable open deep C-type inactivated states (O/I), respectively. The present structures provide an unprecedented view of the selectivity filter backbone in its collapsed deep C-type inactivated conformation, highlighting the close interactions with structural waters and the local allosteric interactions that couple activation and inactivation gating. Together with the structures associated with the closed-inactivated state (C/I) and in the well-known closed conductive state (C/O), this work recapitulates, at atomic resolution, the key conformational changes of a potassium channel pore domain as it progresses along its gating cycle. |
format | Online Article Text |
id | pubmed-5711375 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-57113752017-12-03 The gating cycle of a K(+) channel at atomic resolution Cuello, Luis G Cortes, D Marien Perozo, Eduardo eLife Biochemistry and Chemical Biology C-type inactivation in potassium channels helps fine-tune long-term channel activity through conformational changes at the selectivity filter. Here, through the use of cross-linked constitutively open constructs, we determined the structures of KcsA’s mutants that stabilize the selectivity filter in its conductive (E71A, at 2.25 Å) and deep C-type inactivated (Y82A at 2.4 Å) conformations. These structural snapshots represent KcsA’s transient open-conductive (O/O) and the stable open deep C-type inactivated states (O/I), respectively. The present structures provide an unprecedented view of the selectivity filter backbone in its collapsed deep C-type inactivated conformation, highlighting the close interactions with structural waters and the local allosteric interactions that couple activation and inactivation gating. Together with the structures associated with the closed-inactivated state (C/I) and in the well-known closed conductive state (C/O), this work recapitulates, at atomic resolution, the key conformational changes of a potassium channel pore domain as it progresses along its gating cycle. eLife Sciences Publications, Ltd 2017-11-22 /pmc/articles/PMC5711375/ /pubmed/29165243 http://dx.doi.org/10.7554/eLife.28032 Text en © 2017, Cuello et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Biochemistry and Chemical Biology Cuello, Luis G Cortes, D Marien Perozo, Eduardo The gating cycle of a K(+) channel at atomic resolution |
title | The gating cycle of a K(+) channel at atomic resolution |
title_full | The gating cycle of a K(+) channel at atomic resolution |
title_fullStr | The gating cycle of a K(+) channel at atomic resolution |
title_full_unstemmed | The gating cycle of a K(+) channel at atomic resolution |
title_short | The gating cycle of a K(+) channel at atomic resolution |
title_sort | gating cycle of a k(+) channel at atomic resolution |
topic | Biochemistry and Chemical Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5711375/ https://www.ncbi.nlm.nih.gov/pubmed/29165243 http://dx.doi.org/10.7554/eLife.28032 |
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