Resting state structure of the hyperdepolarization activated two-pore channel 3

Voltage-gated ion channels endow membranes with excitability and the means to propagate action potentials that form the basis of all neuronal signaling. We determined the structure of a voltage-gated sodium channel, two-pore channel 3 (TPC3), which generates ultralong action potentials. TPC3 is dist...

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Veröffentlicht in:Proceedings of the National Academy of Sciences - PNAS 2020-01, Vol.117 (4), p.1988-1993
Hauptverfasser: Dickinson, Miles Sasha, Myasnikov, Alexander, Eriksen, Jacob, Poweleit, Nicole, Stroud, Robert M.
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Sprache:eng
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Zusammenfassung:Voltage-gated ion channels endow membranes with excitability and the means to propagate action potentials that form the basis of all neuronal signaling. We determined the structure of a voltage-gated sodium channel, two-pore channel 3 (TPC3), which generates ultralong action potentials. TPC3 is distinguished by activation only at extreme membrane depolarization (V50 ∼ +75 mV), in contrast to other TPCs and NaV channels that activate between −20 and 0 mV. We present electrophysiological evidence that TPC3 voltage activation depends only on voltage sensing domain 2 (VSD2) and that each of the three gating arginines in VSD2 reduces the activation threshold. The structure presents a chemical basis for sodium selectivity, and a constricted gate suggests a closed pore consistent with extreme voltage dependence. The structure, confirmed by our electrophysiology, illustrates the configuration of a bona fide resting state voltage sensor, observed without the need for any inhibitory ligand, and independent of any chemical or mutagenic alteration.
ISSN:0027-8424
1091-6490
DOI:10.1073/pnas.1915144117