Mechanism of voltage sensing in Ca<sup>2+</sup>- and voltage-activated K<sup>+</sup> (BK) channels.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 35704760.
- Also identified by DOI 10.1073/pnas.2204620119 and PMC identifier 9231616.
- Licence recorded as CC BY-NC-ND.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
In neurosecretion, allosteric communication between voltage sensors and Ca<sup>2+</sup> binding in BK channels is crucially involved in damping excitatory stimuli. Nevertheless, the voltage-sensing mechanism of BK channels is still under debate. Here, based on gating current measurements, we demonstrate that two arginines in the transmembrane segment S4 (R210 and R213) function as the BK gating charges. Significantly, the energy landscape of the gating particles is electrostatically tuned by a network of salt bridges contained in the voltage sensor domain (VSD). Molecular dynamics simulations and proton transport experiments in the hyperpolarization-activated R210H mutant suggest that the electric field drops off within a narrow septum whose boundaries are defined by the gating charges. Unlike Kv channels, the charge movement in BK appears to be limited to a small displacement of the guanidinium moieties of R210 and R213, without significant movement of the S4.
Medical subject headings
- Ion Channel Gating
- Large-Conductance Calcium-Activated Potassium Channels