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Temperature dependence of proton permeation through a voltage-gated proton channel

Voltage-gated proton channels are found in many different types of cells, where they facilitate proton movement through the membrane. The mechanism of proton permeation through the channel is an issue of long-term interest, but it remains an open question. To address this issue, we examined the temp...

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Autores principales: Kuno, Miyuki, Ando, Hiroyuki, Morihata, Hirokazu, Sakai, Hiromu, Mori, Hiroyuki, Sawada, Makoto, Oiki, Shigetoshi
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2740922/
https://www.ncbi.nlm.nih.gov/pubmed/19720960
http://dx.doi.org/10.1085/jgp.200910213
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author Kuno, Miyuki
Ando, Hiroyuki
Morihata, Hirokazu
Sakai, Hiromu
Mori, Hiroyuki
Sawada, Makoto
Oiki, Shigetoshi
author_facet Kuno, Miyuki
Ando, Hiroyuki
Morihata, Hirokazu
Sakai, Hiromu
Mori, Hiroyuki
Sawada, Makoto
Oiki, Shigetoshi
author_sort Kuno, Miyuki
collection PubMed
description Voltage-gated proton channels are found in many different types of cells, where they facilitate proton movement through the membrane. The mechanism of proton permeation through the channel is an issue of long-term interest, but it remains an open question. To address this issue, we examined the temperature dependence of proton permeation. Under whole cell recordings, rapid temperature changes within a few milliseconds were imposed. This method allowed for the measurement of current amplitudes immediately before and after a temperature jump, from which the ratios of these currents (I(ratio)) were determined. The use of I(ratio) for evaluating the temperature dependence minimized the contributions of factors other than permeation. Temperature jumps of various degrees (ΔT, −15 to 15°C) were applied over a wide temperature range (4–49°C), and the Q(10)s for the proton currents were evaluated from the I(ratio)s. Q(10) exhibited a high temperature dependence, varying from 2.2 at 10°C to 1.3 at 40°C. This implies that processes with different temperature dependencies underlie the observed Q(10). A novel resistivity pulse method revealed that the access resistance with its low temperature dependence predominated in high temperature ranges. The measured temperature dependence of Q(10) was decomposed into Q(10) of the channel and of the access resistances. Finally, the Q(10) for proton permeation through the voltage-gated proton channel itself was calculated and found to vary from 2.8 at 5°C to 2.2 at 45°C, as expected for an activation enthalpy of 64 kJ/mol. The thermodynamic features for proton permeation through proton-selective channels were discussed for the underlying mechanism.
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spelling pubmed-27409222010-03-01 Temperature dependence of proton permeation through a voltage-gated proton channel Kuno, Miyuki Ando, Hiroyuki Morihata, Hirokazu Sakai, Hiromu Mori, Hiroyuki Sawada, Makoto Oiki, Shigetoshi J Gen Physiol Article Voltage-gated proton channels are found in many different types of cells, where they facilitate proton movement through the membrane. The mechanism of proton permeation through the channel is an issue of long-term interest, but it remains an open question. To address this issue, we examined the temperature dependence of proton permeation. Under whole cell recordings, rapid temperature changes within a few milliseconds were imposed. This method allowed for the measurement of current amplitudes immediately before and after a temperature jump, from which the ratios of these currents (I(ratio)) were determined. The use of I(ratio) for evaluating the temperature dependence minimized the contributions of factors other than permeation. Temperature jumps of various degrees (ΔT, −15 to 15°C) were applied over a wide temperature range (4–49°C), and the Q(10)s for the proton currents were evaluated from the I(ratio)s. Q(10) exhibited a high temperature dependence, varying from 2.2 at 10°C to 1.3 at 40°C. This implies that processes with different temperature dependencies underlie the observed Q(10). A novel resistivity pulse method revealed that the access resistance with its low temperature dependence predominated in high temperature ranges. The measured temperature dependence of Q(10) was decomposed into Q(10) of the channel and of the access resistances. Finally, the Q(10) for proton permeation through the voltage-gated proton channel itself was calculated and found to vary from 2.8 at 5°C to 2.2 at 45°C, as expected for an activation enthalpy of 64 kJ/mol. The thermodynamic features for proton permeation through proton-selective channels were discussed for the underlying mechanism. The Rockefeller University Press 2009-09 /pmc/articles/PMC2740922/ /pubmed/19720960 http://dx.doi.org/10.1085/jgp.200910213 Text en © 2009 Kuno et al. 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.jgp.org/misc/terms.shtml). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).
spellingShingle Article
Kuno, Miyuki
Ando, Hiroyuki
Morihata, Hirokazu
Sakai, Hiromu
Mori, Hiroyuki
Sawada, Makoto
Oiki, Shigetoshi
Temperature dependence of proton permeation through a voltage-gated proton channel
title Temperature dependence of proton permeation through a voltage-gated proton channel
title_full Temperature dependence of proton permeation through a voltage-gated proton channel
title_fullStr Temperature dependence of proton permeation through a voltage-gated proton channel
title_full_unstemmed Temperature dependence of proton permeation through a voltage-gated proton channel
title_short Temperature dependence of proton permeation through a voltage-gated proton channel
title_sort temperature dependence of proton permeation through a voltage-gated proton channel
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2740922/
https://www.ncbi.nlm.nih.gov/pubmed/19720960
http://dx.doi.org/10.1085/jgp.200910213
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