ML277 specifically enhances the fully activated open state of KCNQ1 by modulating VSD-pore coupling

Upon membrane depolarization, the KCNQ1 potassium channel opens at the intermediate (IO) and activated (AO) states of the stepwise voltage-sensing domain (VSD) activation. In the heart, KCNQ1 associates with KCNE1 subunits to form IKs channels that regulate heart rhythm. KCNE1 suppresses the IO stat...

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Main Authors: Panpan Hou, Jingyi Shi, Kelli McFarland White, Yuan Gao, Jianmin Cui
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2019-07-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/48576
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spelling doaj-fee978959f1d4dbf94c401a4401b1fdf2021-05-05T17:47:10ZengeLife Sciences Publications LtdeLife2050-084X2019-07-01810.7554/eLife.48576ML277 specifically enhances the fully activated open state of KCNQ1 by modulating VSD-pore couplingPanpan Hou0https://orcid.org/0000-0001-7694-2262Jingyi Shi1Kelli McFarland White2Yuan Gao3https://orcid.org/0000-0002-7661-2367Jianmin Cui4https://orcid.org/0000-0002-9198-6332Department of Biomedical Engineering, Washington University, St. Louis, United States; Center for the Investigation of Membrane Excitability Disorders, Washington University, St. Louis, United States; Cardiac Bioelectricity and Arrhythmia Center, Washington University, St. Louis, United StatesDepartment of Biomedical Engineering, Washington University, St. Louis, United States; Center for the Investigation of Membrane Excitability Disorders, Washington University, St. Louis, United States; Cardiac Bioelectricity and Arrhythmia Center, Washington University, St. Louis, United StatesDepartment of Biomedical Engineering, Washington University, St. Louis, United States; Center for the Investigation of Membrane Excitability Disorders, Washington University, St. Louis, United States; Cardiac Bioelectricity and Arrhythmia Center, Washington University, St. Louis, United StatesTencent AI Lab, Shenzhen, ChinaDepartment of Biomedical Engineering, Washington University, St. Louis, United States; Center for the Investigation of Membrane Excitability Disorders, Washington University, St. Louis, United States; Cardiac Bioelectricity and Arrhythmia Center, Washington University, St. Louis, United StatesUpon membrane depolarization, the KCNQ1 potassium channel opens at the intermediate (IO) and activated (AO) states of the stepwise voltage-sensing domain (VSD) activation. In the heart, KCNQ1 associates with KCNE1 subunits to form IKs channels that regulate heart rhythm. KCNE1 suppresses the IO state so that the IKs channel opens only to the AO state. Here, we tested modulations of human KCNQ1 channels by an activator ML277 in Xenopus oocytes. It exclusively changes the pore opening properties of the AO state without altering the IO state, but does not affect VSD activation. These observations support a distinctive mechanism responsible for the VSD-pore coupling at the AO state that is sensitive to ML277 modulation. ML277 provides insights and a tool to investigate the gating mechanism of KCNQ1 channels, and our study reveals a new strategy for treating long QT syndrome by specifically enhancing the AO state of native IKs currents.https://elifesciences.org/articles/48576VSD-pore couplingKCNQ1 channelML277state-dependent activationlong QT syndromeactivated open state
collection DOAJ
language English
format Article
sources DOAJ
author Panpan Hou
Jingyi Shi
Kelli McFarland White
Yuan Gao
Jianmin Cui
spellingShingle Panpan Hou
Jingyi Shi
Kelli McFarland White
Yuan Gao
Jianmin Cui
ML277 specifically enhances the fully activated open state of KCNQ1 by modulating VSD-pore coupling
eLife
VSD-pore coupling
KCNQ1 channel
ML277
state-dependent activation
long QT syndrome
activated open state
author_facet Panpan Hou
Jingyi Shi
Kelli McFarland White
Yuan Gao
Jianmin Cui
author_sort Panpan Hou
title ML277 specifically enhances the fully activated open state of KCNQ1 by modulating VSD-pore coupling
title_short ML277 specifically enhances the fully activated open state of KCNQ1 by modulating VSD-pore coupling
title_full ML277 specifically enhances the fully activated open state of KCNQ1 by modulating VSD-pore coupling
title_fullStr ML277 specifically enhances the fully activated open state of KCNQ1 by modulating VSD-pore coupling
title_full_unstemmed ML277 specifically enhances the fully activated open state of KCNQ1 by modulating VSD-pore coupling
title_sort ml277 specifically enhances the fully activated open state of kcnq1 by modulating vsd-pore coupling
publisher eLife Sciences Publications Ltd
series eLife
issn 2050-084X
publishDate 2019-07-01
description Upon membrane depolarization, the KCNQ1 potassium channel opens at the intermediate (IO) and activated (AO) states of the stepwise voltage-sensing domain (VSD) activation. In the heart, KCNQ1 associates with KCNE1 subunits to form IKs channels that regulate heart rhythm. KCNE1 suppresses the IO state so that the IKs channel opens only to the AO state. Here, we tested modulations of human KCNQ1 channels by an activator ML277 in Xenopus oocytes. It exclusively changes the pore opening properties of the AO state without altering the IO state, but does not affect VSD activation. These observations support a distinctive mechanism responsible for the VSD-pore coupling at the AO state that is sensitive to ML277 modulation. ML277 provides insights and a tool to investigate the gating mechanism of KCNQ1 channels, and our study reveals a new strategy for treating long QT syndrome by specifically enhancing the AO state of native IKs currents.
topic VSD-pore coupling
KCNQ1 channel
ML277
state-dependent activation
long QT syndrome
activated open state
url https://elifesciences.org/articles/48576
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AT kellimcfarlandwhite ml277specificallyenhancesthefullyactivatedopenstateofkcnq1bymodulatingvsdporecoupling
AT yuangao ml277specificallyenhancesthefullyactivatedopenstateofkcnq1bymodulatingvsdporecoupling
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