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A Voltage Sensor-Domain Protein Is a Voltage-Gated Proton Channel

Authors: Mari, Sasaki; Masahiro, Takagi; Yasushi, Okamura;

A Voltage Sensor-Domain Protein Is a Voltage-Gated Proton Channel

Abstract

Voltage-gated proton channels have been widely observed but have not been identified at a molecular level. Here we report that a four-transmembrane protein similar to the voltage-sensor domain of voltage-gated ion channels is a voltage-gated proton channel. Cells overexpressing this protein showed depolarization-induced outward currents accompanied by tail currents. Current reversal occured at equilibrium potentials for protons. The currents exhibited pH-dependent gating and zinc ion sensitivity, two features which are characteristic of voltage-gated proton channels. Responses of voltage dependence to sequence changes suggest that mouse voltage-sensor domain–only protein is itself a channel, rather than a regulator of another channel protein.

Keywords

Patch-Clamp Techniques, Molecular Sequence Data, Electric Conductivity, Hydrogen-Ion Concentration, Transfection, Ion Channels, Cell Line, Ciona intestinalis, Membrane Potentials, Protein Structure, Tertiary, Mice, Mutation, Animals, Humans, Protons, Ion Channel Gating

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Powered by OpenAIRE graph
Found an issue? Give us feedback
selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
512
Top 1%
Top 1%
Top 1%
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