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Mechanism of Electromechanical Coupling in Voltage-Gated Potassium Channels

Voltage-gated ion channels play a central role in the generation of action potentials in the nervous system. They are selective for one type of ion – sodium, calcium, or potassium. Voltage-gated ion channels are composed of a central pore that allows ions to pass through the membrane and four periph...

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Autores principales: Blunck, Rikard, Batulan, Zarah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3439648/
https://www.ncbi.nlm.nih.gov/pubmed/22988442
http://dx.doi.org/10.3389/fphar.2012.00166
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author Blunck, Rikard
Batulan, Zarah
author_facet Blunck, Rikard
Batulan, Zarah
author_sort Blunck, Rikard
collection PubMed
description Voltage-gated ion channels play a central role in the generation of action potentials in the nervous system. They are selective for one type of ion – sodium, calcium, or potassium. Voltage-gated ion channels are composed of a central pore that allows ions to pass through the membrane and four peripheral voltage sensing domains that respond to changes in the membrane potential. Upon depolarization, voltage sensors in voltage-gated potassium channels (Kv) undergo conformational changes driven by positive charges in the S4 segment and aided by pairwise electrostatic interactions with the surrounding voltage sensor. Structure-function relations of Kv channels have been investigated in detail, and the resulting models on the movement of the voltage sensors now converge to a consensus; the S4 segment undergoes a combined movement of rotation, tilt, and vertical displacement in order to bring 3–4e(+) each through the electric field focused in this region. Nevertheless, the mechanism by which the voltage sensor movement leads to pore opening, the electromechanical coupling, is still not fully understood. Thus, recently, electromechanical coupling in different Kv channels has been investigated with a multitude of techniques including electrophysiology, 3D crystal structures, fluorescence spectroscopy, and molecular dynamics simulations. Evidently, the S4–S5 linker, the covalent link between the voltage sensor and pore, plays a crucial role. The linker transfers the energy from the voltage sensor movement to the pore domain via an interaction with the S6 C-termini, which are pulled open during gating. In addition, other contact regions have been proposed. This review aims to provide (i) an in-depth comparison of the molecular mechanisms of electromechanical coupling in different Kv channels; (ii) insight as to how the voltage sensor and pore domain influence one another; and (iii) theoretical predictions on the movement of the cytosolic face of the Kv channels during gating.
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spelling pubmed-34396482012-09-17 Mechanism of Electromechanical Coupling in Voltage-Gated Potassium Channels Blunck, Rikard Batulan, Zarah Front Pharmacol Pharmacology Voltage-gated ion channels play a central role in the generation of action potentials in the nervous system. They are selective for one type of ion – sodium, calcium, or potassium. Voltage-gated ion channels are composed of a central pore that allows ions to pass through the membrane and four peripheral voltage sensing domains that respond to changes in the membrane potential. Upon depolarization, voltage sensors in voltage-gated potassium channels (Kv) undergo conformational changes driven by positive charges in the S4 segment and aided by pairwise electrostatic interactions with the surrounding voltage sensor. Structure-function relations of Kv channels have been investigated in detail, and the resulting models on the movement of the voltage sensors now converge to a consensus; the S4 segment undergoes a combined movement of rotation, tilt, and vertical displacement in order to bring 3–4e(+) each through the electric field focused in this region. Nevertheless, the mechanism by which the voltage sensor movement leads to pore opening, the electromechanical coupling, is still not fully understood. Thus, recently, electromechanical coupling in different Kv channels has been investigated with a multitude of techniques including electrophysiology, 3D crystal structures, fluorescence spectroscopy, and molecular dynamics simulations. Evidently, the S4–S5 linker, the covalent link between the voltage sensor and pore, plays a crucial role. The linker transfers the energy from the voltage sensor movement to the pore domain via an interaction with the S6 C-termini, which are pulled open during gating. In addition, other contact regions have been proposed. This review aims to provide (i) an in-depth comparison of the molecular mechanisms of electromechanical coupling in different Kv channels; (ii) insight as to how the voltage sensor and pore domain influence one another; and (iii) theoretical predictions on the movement of the cytosolic face of the Kv channels during gating. Frontiers Research Foundation 2012-09-12 /pmc/articles/PMC3439648/ /pubmed/22988442 http://dx.doi.org/10.3389/fphar.2012.00166 Text en Copyright © 2012 Blunck and Batulan. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Pharmacology
Blunck, Rikard
Batulan, Zarah
Mechanism of Electromechanical Coupling in Voltage-Gated Potassium Channels
title Mechanism of Electromechanical Coupling in Voltage-Gated Potassium Channels
title_full Mechanism of Electromechanical Coupling in Voltage-Gated Potassium Channels
title_fullStr Mechanism of Electromechanical Coupling in Voltage-Gated Potassium Channels
title_full_unstemmed Mechanism of Electromechanical Coupling in Voltage-Gated Potassium Channels
title_short Mechanism of Electromechanical Coupling in Voltage-Gated Potassium Channels
title_sort mechanism of electromechanical coupling in voltage-gated potassium channels
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3439648/
https://www.ncbi.nlm.nih.gov/pubmed/22988442
http://dx.doi.org/10.3389/fphar.2012.00166
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