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Conduction through the Inward Rectifier Potassium Channel, Kir2.1, Is Increased by Negatively Charged Extracellular Residues
Ion channel conductance can be influenced by electrostatic effects originating from fixed “surface” charges that are remote from the selectivity filter. To explore whether surface charges contribute to the conductance properties of Kir2.1 channels, unitary conductance was measured in cell-attached r...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2217506/ https://www.ncbi.nlm.nih.gov/pubmed/15824191 http://dx.doi.org/10.1085/jgp.200409175 |
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author | D'Avanzo, Nazzareno Cho, Hee Cheol Tolokh, Illya Pekhletski, Roman Tolokh, Igor Gray, Chris Goldman, Saul Backx, Peter H. |
author_facet | D'Avanzo, Nazzareno Cho, Hee Cheol Tolokh, Illya Pekhletski, Roman Tolokh, Igor Gray, Chris Goldman, Saul Backx, Peter H. |
author_sort | D'Avanzo, Nazzareno |
collection | PubMed |
description | Ion channel conductance can be influenced by electrostatic effects originating from fixed “surface” charges that are remote from the selectivity filter. To explore whether surface charges contribute to the conductance properties of Kir2.1 channels, unitary conductance was measured in cell-attached recordings of Chinese hamster ovary (CHO) cells transfected with Kir2.1 channels over a range of K(+) activities (4.6–293.5 mM) using single-channel measurements as well as nonstationary fluctuation analysis for low K(+) activities. K(+) ion concentrations were shown to equilibrate across the cell membrane in our studies using the voltage-sensitive dye DiBAC(4)(5). The dependence of γ on the K(+) activity (a(K)) was fit well by a modified Langmuir binding isotherm, with a nonzero intercept as a(K) approaches 0 mM, suggesting electrostatic surface charge effects. Following the addition of 100 mM N-methyl-d-glucamine (NMG(+)), a nonpermeant, nonblocking cation or following pretreatment with 50 mM trimethyloxonium (TMO), a carboxylic acid esterifying agent, the γ–a(K) relationship did not show nonzero intercepts, suggesting the presence of surface charges formed by glutamate or aspartate residues. Consistent with surface charges in Kir2.1 channels, the rates of current decay induced by Ba(2+) block were slowed with the addition of NMG or TMO. Using a molecular model of Kir2.1 channels, three candidate negatively charged residues were identified near the extracellular mouth of the pore and mutated to cysteine (E125C, D152C, and E153C). E153C channels, but not E125C or D152C channels, showed hyperbolic γ–a(K) relationships going through the origin. Moreover, the addition of MTSES to restore the negative charges in E53C channels reestablished wild-type conductance properties. Our results demonstrate that E153 contributes to the conductance properties of Kir2.1 channels by acting as a surface charge. |
format | Text |
id | pubmed-2217506 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-22175062008-03-21 Conduction through the Inward Rectifier Potassium Channel, Kir2.1, Is Increased by Negatively Charged Extracellular Residues D'Avanzo, Nazzareno Cho, Hee Cheol Tolokh, Illya Pekhletski, Roman Tolokh, Igor Gray, Chris Goldman, Saul Backx, Peter H. J Gen Physiol Article Ion channel conductance can be influenced by electrostatic effects originating from fixed “surface” charges that are remote from the selectivity filter. To explore whether surface charges contribute to the conductance properties of Kir2.1 channels, unitary conductance was measured in cell-attached recordings of Chinese hamster ovary (CHO) cells transfected with Kir2.1 channels over a range of K(+) activities (4.6–293.5 mM) using single-channel measurements as well as nonstationary fluctuation analysis for low K(+) activities. K(+) ion concentrations were shown to equilibrate across the cell membrane in our studies using the voltage-sensitive dye DiBAC(4)(5). The dependence of γ on the K(+) activity (a(K)) was fit well by a modified Langmuir binding isotherm, with a nonzero intercept as a(K) approaches 0 mM, suggesting electrostatic surface charge effects. Following the addition of 100 mM N-methyl-d-glucamine (NMG(+)), a nonpermeant, nonblocking cation or following pretreatment with 50 mM trimethyloxonium (TMO), a carboxylic acid esterifying agent, the γ–a(K) relationship did not show nonzero intercepts, suggesting the presence of surface charges formed by glutamate or aspartate residues. Consistent with surface charges in Kir2.1 channels, the rates of current decay induced by Ba(2+) block were slowed with the addition of NMG or TMO. Using a molecular model of Kir2.1 channels, three candidate negatively charged residues were identified near the extracellular mouth of the pore and mutated to cysteine (E125C, D152C, and E153C). E153C channels, but not E125C or D152C channels, showed hyperbolic γ–a(K) relationships going through the origin. Moreover, the addition of MTSES to restore the negative charges in E53C channels reestablished wild-type conductance properties. Our results demonstrate that E153 contributes to the conductance properties of Kir2.1 channels by acting as a surface charge. The Rockefeller University Press 2005-05 /pmc/articles/PMC2217506/ /pubmed/15824191 http://dx.doi.org/10.1085/jgp.200409175 Text en Copyright © 2005, 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 | Article D'Avanzo, Nazzareno Cho, Hee Cheol Tolokh, Illya Pekhletski, Roman Tolokh, Igor Gray, Chris Goldman, Saul Backx, Peter H. Conduction through the Inward Rectifier Potassium Channel, Kir2.1, Is Increased by Negatively Charged Extracellular Residues |
title | Conduction through the Inward Rectifier Potassium Channel, Kir2.1, Is Increased by Negatively Charged Extracellular Residues |
title_full | Conduction through the Inward Rectifier Potassium Channel, Kir2.1, Is Increased by Negatively Charged Extracellular Residues |
title_fullStr | Conduction through the Inward Rectifier Potassium Channel, Kir2.1, Is Increased by Negatively Charged Extracellular Residues |
title_full_unstemmed | Conduction through the Inward Rectifier Potassium Channel, Kir2.1, Is Increased by Negatively Charged Extracellular Residues |
title_short | Conduction through the Inward Rectifier Potassium Channel, Kir2.1, Is Increased by Negatively Charged Extracellular Residues |
title_sort | conduction through the inward rectifier potassium channel, kir2.1, is increased by negatively charged extracellular residues |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2217506/ https://www.ncbi.nlm.nih.gov/pubmed/15824191 http://dx.doi.org/10.1085/jgp.200409175 |
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