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A Quantitative Description of KcsA Gating II: Single-Channel Currents

The kinetic transitions of proton-activated WT KcsA and the noninactivating E71A mutant were studied at the single-channel level in purified, liposome-reconstituted preparations. Single-channel currents were recorded using patch-clamp techniques under nonstationary and steady-state conditions. Maxim...

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Autores principales: Chakrapani, Sudha, Cordero-Morales, Julio F, Perozo, Eduardo
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2151667/
https://www.ncbi.nlm.nih.gov/pubmed/17938231
http://dx.doi.org/10.1085/jgp.200709844
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author Chakrapani, Sudha
Cordero-Morales, Julio F
Perozo, Eduardo
author_facet Chakrapani, Sudha
Cordero-Morales, Julio F
Perozo, Eduardo
author_sort Chakrapani, Sudha
collection PubMed
description The kinetic transitions of proton-activated WT KcsA and the noninactivating E71A mutant were studied at the single-channel level in purified, liposome-reconstituted preparations. Single-channel currents were recorded using patch-clamp techniques under nonstationary and steady-state conditions. Maximum-likelihood analyses reveal that the key influence of acidic pH is to increase the frequency of bursting without an effect on the intraburst open and closed dwell times, consistent with the finding from macroscopic currents that protons promote activation without a significant effect on inactivation. However, in steady-conditions of pH, voltage not only alters the burst frequency but also affects their properties, such as the frequency of the flickers and the dwell times of the closed and open states. This is to be expected if voltage modulates pathways connecting open and inactivated states. Upon opening, KcsA can enter at least two closed states that are not part of the activation pathway. The frequency and duration of these closed states was found to be voltage dependent and therefore these are likely to represent short-lived inactivated states. Single-channel recordings of WT KcsA also show varying propensity for the presence of subconductance states. The probability of occurrence of these states did not show clear modulation by voltage or pH and their origin remains unclear and a focus for further investigation. A kinetic model is proposed to describe the gating events in KcsA that recapitulates its macroscopic and single-channel behavior. The model has been constrained by the single-channel analyses presented in this work along with data from macroscopic currents in the preceding paper.
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spelling pubmed-21516672008-04-30 A Quantitative Description of KcsA Gating II: Single-Channel Currents Chakrapani, Sudha Cordero-Morales, Julio F Perozo, Eduardo J Gen Physiol Articles The kinetic transitions of proton-activated WT KcsA and the noninactivating E71A mutant were studied at the single-channel level in purified, liposome-reconstituted preparations. Single-channel currents were recorded using patch-clamp techniques under nonstationary and steady-state conditions. Maximum-likelihood analyses reveal that the key influence of acidic pH is to increase the frequency of bursting without an effect on the intraburst open and closed dwell times, consistent with the finding from macroscopic currents that protons promote activation without a significant effect on inactivation. However, in steady-conditions of pH, voltage not only alters the burst frequency but also affects their properties, such as the frequency of the flickers and the dwell times of the closed and open states. This is to be expected if voltage modulates pathways connecting open and inactivated states. Upon opening, KcsA can enter at least two closed states that are not part of the activation pathway. The frequency and duration of these closed states was found to be voltage dependent and therefore these are likely to represent short-lived inactivated states. Single-channel recordings of WT KcsA also show varying propensity for the presence of subconductance states. The probability of occurrence of these states did not show clear modulation by voltage or pH and their origin remains unclear and a focus for further investigation. A kinetic model is proposed to describe the gating events in KcsA that recapitulates its macroscopic and single-channel behavior. The model has been constrained by the single-channel analyses presented in this work along with data from macroscopic currents in the preceding paper. The Rockefeller University Press 2007-11 /pmc/articles/PMC2151667/ /pubmed/17938231 http://dx.doi.org/10.1085/jgp.200709844 Text en Copyright © 2007, 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 Articles
Chakrapani, Sudha
Cordero-Morales, Julio F
Perozo, Eduardo
A Quantitative Description of KcsA Gating II: Single-Channel Currents
title A Quantitative Description of KcsA Gating II: Single-Channel Currents
title_full A Quantitative Description of KcsA Gating II: Single-Channel Currents
title_fullStr A Quantitative Description of KcsA Gating II: Single-Channel Currents
title_full_unstemmed A Quantitative Description of KcsA Gating II: Single-Channel Currents
title_short A Quantitative Description of KcsA Gating II: Single-Channel Currents
title_sort quantitative description of kcsa gating ii: single-channel currents
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2151667/
https://www.ncbi.nlm.nih.gov/pubmed/17938231
http://dx.doi.org/10.1085/jgp.200709844
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