| Literature DB >> 33783354 |
Monica L Fernández-Quintero1,2, Yousra El Ghaleb1, Petronel Tuluc3, Marta Campiglio1, Klaus R Liedl2, Bernhard E Flucher1.
Abstract
Voltage-gated calcium channels control key functions of excitable cells, like synaptic transmission in neurons and the contraction of heart and skeletal muscles. To accomplish such diverse functions, different calcium channels activate at different voltages and with distinct kinetics. To identify the molecular mechanisms governing specific voltage sensing properties, we combined structure modeling, mutagenesis, and electrophysiology to analyze the structures, free energy, and transition kinetics of the activated and resting states of two functionally distinct voltage sensing domains (VSDs) of the eukaryotic calcium channel CaV1.1. Both VSDs displayed the typical features of the sliding helix model; however, they greatly differed in ion-pair formation of the outer gating charges. Specifically, stabilization of the activated state enhanced the voltage dependence of activation, while stabilization of resting states slowed the kinetics. This mechanism provides a mechanistic model explaining how specific ion-pair formation in separate VSDs can realize the characteristic gating properties of voltage-gated cation channels.Entities:
Keywords: CaV1.1; molecular biophysics; molecular dynamics simulation; mouse; neuroscience; resting state structure; structural biology; voltage sensing; voltage-gated calcium channel
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Year: 2021 PMID: 33783354 PMCID: PMC8099428 DOI: 10.7554/eLife.64087
Source DB: PubMed Journal: Elife ISSN: 2050-084X Impact factor: 8.713