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The structural basis of divalent cation block in a tetrameric prokaryotic sodium channel
Divalent cation block is observed in various tetrameric ion channels. For blocking, a divalent cation is thought to bind in the ion pathway of the channel, but such block has not yet been directly observed. So, the behaviour of these blocking divalent cations remains still uncertain. Here, we elucid...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10349818/ https://www.ncbi.nlm.nih.gov/pubmed/37454189 http://dx.doi.org/10.1038/s41467-023-39987-0 |
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author | Irie, Katsumasa Oda, Yoshinori Sumikama, Takashi Oshima, Atsunori Fujiyoshi, Yoshinori |
author_facet | Irie, Katsumasa Oda, Yoshinori Sumikama, Takashi Oshima, Atsunori Fujiyoshi, Yoshinori |
author_sort | Irie, Katsumasa |
collection | PubMed |
description | Divalent cation block is observed in various tetrameric ion channels. For blocking, a divalent cation is thought to bind in the ion pathway of the channel, but such block has not yet been directly observed. So, the behaviour of these blocking divalent cations remains still uncertain. Here, we elucidated the mechanism of the divalent cation block by reproducing the blocking effect into NavAb, a well-studied tetrameric sodium channel. Our crystal structures of NavAb mutants show that the mutations increasing the hydrophilicity of the inner vestibule of the pore domain enable a divalent cation to stack on the ion pathway. Furthermore, non-equilibrium molecular dynamics simulation showed that the stacking calcium ion repel sodium ion at the bottom of the selectivity filter. These results suggest the primary process of the divalent cation block mechanism in tetrameric cation channels. |
format | Online Article Text |
id | pubmed-10349818 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-103498182023-07-17 The structural basis of divalent cation block in a tetrameric prokaryotic sodium channel Irie, Katsumasa Oda, Yoshinori Sumikama, Takashi Oshima, Atsunori Fujiyoshi, Yoshinori Nat Commun Article Divalent cation block is observed in various tetrameric ion channels. For blocking, a divalent cation is thought to bind in the ion pathway of the channel, but such block has not yet been directly observed. So, the behaviour of these blocking divalent cations remains still uncertain. Here, we elucidated the mechanism of the divalent cation block by reproducing the blocking effect into NavAb, a well-studied tetrameric sodium channel. Our crystal structures of NavAb mutants show that the mutations increasing the hydrophilicity of the inner vestibule of the pore domain enable a divalent cation to stack on the ion pathway. Furthermore, non-equilibrium molecular dynamics simulation showed that the stacking calcium ion repel sodium ion at the bottom of the selectivity filter. These results suggest the primary process of the divalent cation block mechanism in tetrameric cation channels. Nature Publishing Group UK 2023-07-15 /pmc/articles/PMC10349818/ /pubmed/37454189 http://dx.doi.org/10.1038/s41467-023-39987-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Irie, Katsumasa Oda, Yoshinori Sumikama, Takashi Oshima, Atsunori Fujiyoshi, Yoshinori The structural basis of divalent cation block in a tetrameric prokaryotic sodium channel |
title | The structural basis of divalent cation block in a tetrameric prokaryotic sodium channel |
title_full | The structural basis of divalent cation block in a tetrameric prokaryotic sodium channel |
title_fullStr | The structural basis of divalent cation block in a tetrameric prokaryotic sodium channel |
title_full_unstemmed | The structural basis of divalent cation block in a tetrameric prokaryotic sodium channel |
title_short | The structural basis of divalent cation block in a tetrameric prokaryotic sodium channel |
title_sort | structural basis of divalent cation block in a tetrameric prokaryotic sodium channel |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10349818/ https://www.ncbi.nlm.nih.gov/pubmed/37454189 http://dx.doi.org/10.1038/s41467-023-39987-0 |
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