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Voltage-gated proton channel C

Unless otherwise stated all data on this page refer to the human proteins. Gene information is provided for human (Hs), mouse (Mm) and rat (Rn).

Overview

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The voltage-gated proton channel (provisionally denoted Hv1) is a putative 4TM proton-selective channel gated by membrane depolarization and which is sensitive to the transmembrane pH gradient [1,5-6,26,28]. The structure of Hv1 is homologous to the voltage sensing domain (VSD) of the superfamily of voltage-gated ion channels (i.e. segments S1 to S4) and contains no discernable pore region [26,28]. Proton flux through Hv1 is instead most likely mediated by a hydrogen-bonded chain [23] [4] formed in a crevice of the protein when the voltage-sensing S4 helix moves in response to a change in transmembrane potential [25,33]. Proton selective conduction requires an aspartate residue at the center of the pore [2,22,30]. Both selectivity and conduction may result from obligatory protonation by each conducted proton [8,11]. Hv1 expresses largely as a dimer mediated by intracellular C-terminal coiled-coil interactions [18] but individual promoters nonetheless support gated H+ flux via separate conduction pathways [16-17,24,31]. Within dimeric structures, the two protomers do not function independently, but display co-operative interactions during gating resulting in increased voltage sensitivity, but slower activation, of the dimeric, versus monomeric, complexes [13,32].

Channels and Subunits

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Hv1 C Show summary »

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How to cite this family page

Database page citation:

Voltage-gated proton channel. Accessed on 29/11/2020. IUPHAR/BPS Guide to PHARMACOLOGY, http://www.guidetopharmacology.org/GRAC/FamilyDisplayForward?familyId=124.

Concise Guide to PHARMACOLOGY citation:

Alexander SPH, Mathie A, Peters JA, Veale EL, Striessnig J, Kelly E, Armstrong JF, Faccenda E, Harding SD, Pawson AJ, Sharman JL, Southan C, Davies JA; CGTP Collaborators. (2019) The Concise Guide to PHARMACOLOGY 2019/20: Ion channels. Br J Pharmacol. 176 Issue S1: S142-228.