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Integrated Allosteric Model of Voltage Gating of Hcn Channels

Hyperpolarization-activated (pacemaker) channels are dually gated by negative voltage and intracellular cAMP. Kinetics of native cardiac f-channels are not compatible with HH gating, and require closed/open multistate models. We verified that members of the HCN channel family (mHCN1, hHCN2, hHCN4) a...

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Autores principales: Altomare, Claudia, Bucchi, Annalisa, Camatini, Eva, Baruscotti, Mirko, Viscomi, Carlo, Moroni, Anna, DiFrancesco, Dario
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2001
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2232403/
https://www.ncbi.nlm.nih.gov/pubmed/11382803
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author Altomare, Claudia
Bucchi, Annalisa
Camatini, Eva
Baruscotti, Mirko
Viscomi, Carlo
Moroni, Anna
DiFrancesco, Dario
author_facet Altomare, Claudia
Bucchi, Annalisa
Camatini, Eva
Baruscotti, Mirko
Viscomi, Carlo
Moroni, Anna
DiFrancesco, Dario
author_sort Altomare, Claudia
collection PubMed
description Hyperpolarization-activated (pacemaker) channels are dually gated by negative voltage and intracellular cAMP. Kinetics of native cardiac f-channels are not compatible with HH gating, and require closed/open multistate models. We verified that members of the HCN channel family (mHCN1, hHCN2, hHCN4) also have properties not complying with HH gating, such as sigmoidal activation and deactivation, activation deviating from fixed power of an exponential, removal of activation “delay” by preconditioning hyperpolarization. Previous work on native channels has indicated that the shifting action of cAMP on the open probability (Po) curve can be accounted for by an allosteric model, whereby cAMP binds more favorably to open than closed channels. We therefore asked whether not only cAMP-dependent, but also voltage-dependent gating of hyperpolarization-activated channels could be explained by an allosteric model. We hypothesized that HCN channels are tetramers and that each subunit comprises a voltage sensor moving between “reluctant” and “willing” states, whereas voltage sensors are independently gated by voltage, channel closed/open transitions occur allosterically. These hypotheses led to a multistate scheme comprising five open and five closed channel states. We estimated model rate constants by fitting first activation delay curves and single exponential time constant curves, and then individual activation/deactivation traces. By simply using different sets of rate constants, the model accounts for qualitative and quantitative aspects of voltage gating of all three HCN isoforms investigated, and allows an interpretation of the different kinetic properties of different isoforms. For example, faster kinetics of HCN1 relative to HCN2/HCN4 are attributable to higher HCN1 voltage sensors' rates and looser voltage-independent interactions between subunits in closed/open transitions. It also accounts for experimental evidence that reduction of sensors' positive charge leads to negative voltage shifts of Po curve, with little change of curve slope. HCN voltage gating thus involves two processes: voltage sensor gating and allosteric opening/closing.
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spelling pubmed-22324032008-04-22 Integrated Allosteric Model of Voltage Gating of Hcn Channels Altomare, Claudia Bucchi, Annalisa Camatini, Eva Baruscotti, Mirko Viscomi, Carlo Moroni, Anna DiFrancesco, Dario J Gen Physiol Original Article Hyperpolarization-activated (pacemaker) channels are dually gated by negative voltage and intracellular cAMP. Kinetics of native cardiac f-channels are not compatible with HH gating, and require closed/open multistate models. We verified that members of the HCN channel family (mHCN1, hHCN2, hHCN4) also have properties not complying with HH gating, such as sigmoidal activation and deactivation, activation deviating from fixed power of an exponential, removal of activation “delay” by preconditioning hyperpolarization. Previous work on native channels has indicated that the shifting action of cAMP on the open probability (Po) curve can be accounted for by an allosteric model, whereby cAMP binds more favorably to open than closed channels. We therefore asked whether not only cAMP-dependent, but also voltage-dependent gating of hyperpolarization-activated channels could be explained by an allosteric model. We hypothesized that HCN channels are tetramers and that each subunit comprises a voltage sensor moving between “reluctant” and “willing” states, whereas voltage sensors are independently gated by voltage, channel closed/open transitions occur allosterically. These hypotheses led to a multistate scheme comprising five open and five closed channel states. We estimated model rate constants by fitting first activation delay curves and single exponential time constant curves, and then individual activation/deactivation traces. By simply using different sets of rate constants, the model accounts for qualitative and quantitative aspects of voltage gating of all three HCN isoforms investigated, and allows an interpretation of the different kinetic properties of different isoforms. For example, faster kinetics of HCN1 relative to HCN2/HCN4 are attributable to higher HCN1 voltage sensors' rates and looser voltage-independent interactions between subunits in closed/open transitions. It also accounts for experimental evidence that reduction of sensors' positive charge leads to negative voltage shifts of Po curve, with little change of curve slope. HCN voltage gating thus involves two processes: voltage sensor gating and allosteric opening/closing. The Rockefeller University Press 2001-06-01 /pmc/articles/PMC2232403/ /pubmed/11382803 Text en © 2001 The Rockefeller University Press 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 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Original Article
Altomare, Claudia
Bucchi, Annalisa
Camatini, Eva
Baruscotti, Mirko
Viscomi, Carlo
Moroni, Anna
DiFrancesco, Dario
Integrated Allosteric Model of Voltage Gating of Hcn Channels
title Integrated Allosteric Model of Voltage Gating of Hcn Channels
title_full Integrated Allosteric Model of Voltage Gating of Hcn Channels
title_fullStr Integrated Allosteric Model of Voltage Gating of Hcn Channels
title_full_unstemmed Integrated Allosteric Model of Voltage Gating of Hcn Channels
title_short Integrated Allosteric Model of Voltage Gating of Hcn Channels
title_sort integrated allosteric model of voltage gating of hcn channels
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2232403/
https://www.ncbi.nlm.nih.gov/pubmed/11382803
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