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Structure and physiological function of the human KCNQ1 channel voltage sensor intermediate state
Voltage-gated ion channels feature voltage sensor domains (VSDs) that exist in three distinct conformations during activation: resting, intermediate, and activated. Experimental determination of the structure of a potassium channel VSD in the intermediate state has previously proven elusive. Here, w...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7069725/ https://www.ncbi.nlm.nih.gov/pubmed/32096762 http://dx.doi.org/10.7554/eLife.53901 |
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author | Taylor, Keenan C Kang, Po Wei Hou, Panpan Yang, Nien-Du Kuenze, Georg Smith, Jarrod A Shi, Jingyi Huang, Hui White, Kelli McFarland Peng, Dungeng George, Alfred L Meiler, Jens McFeeters, Robert L Cui, Jianmin Sanders, Charles R |
author_facet | Taylor, Keenan C Kang, Po Wei Hou, Panpan Yang, Nien-Du Kuenze, Georg Smith, Jarrod A Shi, Jingyi Huang, Hui White, Kelli McFarland Peng, Dungeng George, Alfred L Meiler, Jens McFeeters, Robert L Cui, Jianmin Sanders, Charles R |
author_sort | Taylor, Keenan C |
collection | PubMed |
description | Voltage-gated ion channels feature voltage sensor domains (VSDs) that exist in three distinct conformations during activation: resting, intermediate, and activated. Experimental determination of the structure of a potassium channel VSD in the intermediate state has previously proven elusive. Here, we report and validate the experimental three-dimensional structure of the human KCNQ1 voltage-gated potassium channel VSD in the intermediate state. We also used mutagenesis and electrophysiology in Xenopus laevisoocytes to functionally map the determinants of S4 helix motion during voltage-dependent transition from the intermediate to the activated state. Finally, the physiological relevance of the intermediate state KCNQ1 conductance is demonstrated using voltage-clamp fluorometry. This work illuminates the structure of the VSD intermediate state and demonstrates that intermediate state conductivity contributes to the unusual versatility of KCNQ1, which can function either as the slow delayed rectifier current (I(Ks)) of the cardiac action potential or as a constitutively active epithelial leak current. |
format | Online Article Text |
id | pubmed-7069725 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-70697252020-03-18 Structure and physiological function of the human KCNQ1 channel voltage sensor intermediate state Taylor, Keenan C Kang, Po Wei Hou, Panpan Yang, Nien-Du Kuenze, Georg Smith, Jarrod A Shi, Jingyi Huang, Hui White, Kelli McFarland Peng, Dungeng George, Alfred L Meiler, Jens McFeeters, Robert L Cui, Jianmin Sanders, Charles R eLife Structural Biology and Molecular Biophysics Voltage-gated ion channels feature voltage sensor domains (VSDs) that exist in three distinct conformations during activation: resting, intermediate, and activated. Experimental determination of the structure of a potassium channel VSD in the intermediate state has previously proven elusive. Here, we report and validate the experimental three-dimensional structure of the human KCNQ1 voltage-gated potassium channel VSD in the intermediate state. We also used mutagenesis and electrophysiology in Xenopus laevisoocytes to functionally map the determinants of S4 helix motion during voltage-dependent transition from the intermediate to the activated state. Finally, the physiological relevance of the intermediate state KCNQ1 conductance is demonstrated using voltage-clamp fluorometry. This work illuminates the structure of the VSD intermediate state and demonstrates that intermediate state conductivity contributes to the unusual versatility of KCNQ1, which can function either as the slow delayed rectifier current (I(Ks)) of the cardiac action potential or as a constitutively active epithelial leak current. eLife Sciences Publications, Ltd 2020-02-25 /pmc/articles/PMC7069725/ /pubmed/32096762 http://dx.doi.org/10.7554/eLife.53901 Text en © 2020, Taylor 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 | Structural Biology and Molecular Biophysics Taylor, Keenan C Kang, Po Wei Hou, Panpan Yang, Nien-Du Kuenze, Georg Smith, Jarrod A Shi, Jingyi Huang, Hui White, Kelli McFarland Peng, Dungeng George, Alfred L Meiler, Jens McFeeters, Robert L Cui, Jianmin Sanders, Charles R Structure and physiological function of the human KCNQ1 channel voltage sensor intermediate state |
title | Structure and physiological function of the human KCNQ1 channel voltage sensor intermediate state |
title_full | Structure and physiological function of the human KCNQ1 channel voltage sensor intermediate state |
title_fullStr | Structure and physiological function of the human KCNQ1 channel voltage sensor intermediate state |
title_full_unstemmed | Structure and physiological function of the human KCNQ1 channel voltage sensor intermediate state |
title_short | Structure and physiological function of the human KCNQ1 channel voltage sensor intermediate state |
title_sort | structure and physiological function of the human kcnq1 channel voltage sensor intermediate state |
topic | Structural Biology and Molecular Biophysics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7069725/ https://www.ncbi.nlm.nih.gov/pubmed/32096762 http://dx.doi.org/10.7554/eLife.53901 |
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