Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: D'Avanzo, Nazzareno, Cho, Hee Cheol, Tolokh, Illya, Pekhletski, Roman, Tolokh, Igor, Gray, Chris, Goldman, Saul, Backx, Peter H.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2005
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
_version_ 1782149268733165568
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
work_keys_str_mv AT davanzonazzareno conductionthroughtheinwardrectifierpotassiumchannelkir21isincreasedbynegativelychargedextracellularresidues
AT choheecheol conductionthroughtheinwardrectifierpotassiumchannelkir21isincreasedbynegativelychargedextracellularresidues
AT tolokhillya conductionthroughtheinwardrectifierpotassiumchannelkir21isincreasedbynegativelychargedextracellularresidues
AT pekhletskiroman conductionthroughtheinwardrectifierpotassiumchannelkir21isincreasedbynegativelychargedextracellularresidues
AT tolokhigor conductionthroughtheinwardrectifierpotassiumchannelkir21isincreasedbynegativelychargedextracellularresidues
AT graychris conductionthroughtheinwardrectifierpotassiumchannelkir21isincreasedbynegativelychargedextracellularresidues
AT goldmansaul conductionthroughtheinwardrectifierpotassiumchannelkir21isincreasedbynegativelychargedextracellularresidues
AT backxpeterh conductionthroughtheinwardrectifierpotassiumchannelkir21isincreasedbynegativelychargedextracellularresidues