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Voltage-sensing domain mode shift is coupled to the activation gate by the N-terminal tail of hERG channels

Human ether-a-go-go–related gene (hERG) potassium channels exhibit unique gating kinetics characterized by unusually slow activation and deactivation. The N terminus of the channel, which contains an amphipathic helix and an unstructured tail, has been shown to be involved in regulation of this slow...

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Autores principales: Tan, Peter S., Perry, Matthew D., Ng, Chai Ann, Vandenberg, Jamie I., Hill, Adam P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3434099/
https://www.ncbi.nlm.nih.gov/pubmed/22891279
http://dx.doi.org/10.1085/jgp.201110761
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author Tan, Peter S.
Perry, Matthew D.
Ng, Chai Ann
Vandenberg, Jamie I.
Hill, Adam P.
author_facet Tan, Peter S.
Perry, Matthew D.
Ng, Chai Ann
Vandenberg, Jamie I.
Hill, Adam P.
author_sort Tan, Peter S.
collection PubMed
description Human ether-a-go-go–related gene (hERG) potassium channels exhibit unique gating kinetics characterized by unusually slow activation and deactivation. The N terminus of the channel, which contains an amphipathic helix and an unstructured tail, has been shown to be involved in regulation of this slow deactivation. However, the mechanism of how this occurs and the connection between voltage-sensing domain (VSD) return and closing of the gate are unclear. To examine this relationship, we have used voltage-clamp fluorometry to simultaneously measure VSD motion and gate closure in N-terminally truncated constructs. We report that mode shifting of the hERG VSD results in a corresponding shift in the voltage-dependent equilibrium of channel closing and that at negative potentials, coupling of the mode-shifted VSD to the gate defines the rate of channel closure. Deletion of the first 25 aa from the N terminus of hERG does not alter mode shifting of the VSD but uncouples the shift from closure of the cytoplasmic gate. Based on these observations, we propose the N-terminal tail as an adaptor that couples voltage sensor return to gate closure to define slow deactivation gating in hERG channels. Furthermore, because the mode shift occurs on a time scale relevant to the cardiac action potential, we suggest a physiological role for this phenomenon in maximizing current flow through hERG channels during repolarization.
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spelling pubmed-34340992013-03-01 Voltage-sensing domain mode shift is coupled to the activation gate by the N-terminal tail of hERG channels Tan, Peter S. Perry, Matthew D. Ng, Chai Ann Vandenberg, Jamie I. Hill, Adam P. J Gen Physiol Article Human ether-a-go-go–related gene (hERG) potassium channels exhibit unique gating kinetics characterized by unusually slow activation and deactivation. The N terminus of the channel, which contains an amphipathic helix and an unstructured tail, has been shown to be involved in regulation of this slow deactivation. However, the mechanism of how this occurs and the connection between voltage-sensing domain (VSD) return and closing of the gate are unclear. To examine this relationship, we have used voltage-clamp fluorometry to simultaneously measure VSD motion and gate closure in N-terminally truncated constructs. We report that mode shifting of the hERG VSD results in a corresponding shift in the voltage-dependent equilibrium of channel closing and that at negative potentials, coupling of the mode-shifted VSD to the gate defines the rate of channel closure. Deletion of the first 25 aa from the N terminus of hERG does not alter mode shifting of the VSD but uncouples the shift from closure of the cytoplasmic gate. Based on these observations, we propose the N-terminal tail as an adaptor that couples voltage sensor return to gate closure to define slow deactivation gating in hERG channels. Furthermore, because the mode shift occurs on a time scale relevant to the cardiac action potential, we suggest a physiological role for this phenomenon in maximizing current flow through hERG channels during repolarization. The Rockefeller University Press 2012-09 /pmc/articles/PMC3434099/ /pubmed/22891279 http://dx.doi.org/10.1085/jgp.201110761 Text en © 2012 Tan et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).
spellingShingle Article
Tan, Peter S.
Perry, Matthew D.
Ng, Chai Ann
Vandenberg, Jamie I.
Hill, Adam P.
Voltage-sensing domain mode shift is coupled to the activation gate by the N-terminal tail of hERG channels
title Voltage-sensing domain mode shift is coupled to the activation gate by the N-terminal tail of hERG channels
title_full Voltage-sensing domain mode shift is coupled to the activation gate by the N-terminal tail of hERG channels
title_fullStr Voltage-sensing domain mode shift is coupled to the activation gate by the N-terminal tail of hERG channels
title_full_unstemmed Voltage-sensing domain mode shift is coupled to the activation gate by the N-terminal tail of hERG channels
title_short Voltage-sensing domain mode shift is coupled to the activation gate by the N-terminal tail of hERG channels
title_sort voltage-sensing domain mode shift is coupled to the activation gate by the n-terminal tail of herg channels
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3434099/
https://www.ncbi.nlm.nih.gov/pubmed/22891279
http://dx.doi.org/10.1085/jgp.201110761
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