Proceedings of the National Academy of Sciences · 2017 · 59 citations · 49 references
Natural SciencesBiophysicsPhysiologyElectrophysiologyIon Channel BiophysicsMolecular PhysiologyCardiac Ion ChannelsChannelopathiesIon Channel ModulationIon Channel PhysiologyIon Channel RegulationIon ChannelsChannelsPotassium Channel FunctionPotassium Channel GatingPotassium Channel PharmacologyPotassium Channel PhysiologyPotassium ChannelopathiesVoltage-dependent Ion ChannelsVoltage-gated Potassium Channels
channels in the physiological voltage range and important for controlling water and salt secretion and absorption. How KCNE1 and KCNE3 subunits modify KCNQ1 channel gating so differently is largely unknown. Here, we use voltage clamp fluorometry to determine how KCNE1 and KCNE3 affect the voltage sensor and the gate of KCNQ1. By separating S4 movement and gate opening by mutations or phosphatidylinositol 4,5-bisphosphate depletion, we show that KCNE1 affects both the S4 movement and the gate, whereas KCNE3 affects the S4 movement and only affects the gate in KCNQ1 if an intact S4-to-gate coupling is present. Further, we show that a triple mutation in the middle of the transmembrane (TM) segment of KCNE3 introduces KCNE1-like effects on the second S4 movement and the gate. In addition, we show that differences in two residues at the external end of the KCNE TM segments underlie differences in the effects of the different KCNEs on the first S4 movement and the voltage sensor-to-gate coupling.
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