Structural highlights
Publication Abstract from PubMed
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 approximately +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.
Resting state structure of the hyperdepolarization activated two-pore channel 3.,Dickinson MS, Myasnikov A, Eriksen J, Poweleit N, Stroud RM Proc Natl Acad Sci U S A. 2020 Jan 10. pii: 1915144117. doi:, 10.1073/pnas.1915144117. PMID:31924746[1]
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
References
- ↑ Dickinson MS, Myasnikov A, Eriksen J, Poweleit N, Stroud RM. Resting state structure of the hyperdepolarization activated two-pore channel 3. Proc Natl Acad Sci U S A. 2020 Jan 10. pii: 1915144117. doi:, 10.1073/pnas.1915144117. PMID:31924746 doi:http://dx.doi.org/10.1073/pnas.1915144117