Abstract
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.
Author supplied keywords
Cite
CITATION STYLE
Dickinson, M. S., Myasnikov, A., Eriksen, J., Poweleit, N., & Stroud, R. M. (2020). Resting state structure of the hyperdepolarization activated two-pore channel 3. Proceedings of the National Academy of Sciences of the United States of America, 117(4), 1988–1993. https://doi.org/10.1073/pnas.1915144117
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.