Key result
Kinetic analysis of gating currents in the mutant N264R voltage-gated proton channel revealed a complex time course with two peaks and a marked Cole-Moore effect, suggesting at least five states.
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This biophysical study demonstrates that the voltage sensor of the monomeric Hv1 channel mutant N264R undergoes complex, multi-state conformational changes during activation.
1 mutant N264R. Isolated ON-gating currents decayed at increasing rates with increasing membrane depolarization, and the amount of gating charges displaced saturates at high voltages. These are two hallmarks of currents arising from the movement of charged elements within the boundaries of the cell membrane. The kinetic analysis of gating currents revealed a complex time course of the ON-gating current characterized by two peaks and a marked Cole-Moore effect. Both features argue that the voltage sensor undergoes several voltage-dependent conformational changes during activation. However, most of the charge is displaced in a single central transition. Upon voltage sensor activation, the charge is trapped, and only a fast component that carries a small percentage of the total charge is observed in the OFF. We hypothesize that trapping is due to the presence of the arginine side chain in position 264, which acts as a blocking ion. We conclude that the movement of the voltage sensor must proceed through at least five states to account for our experimental data satisfactorily.
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Carmona et al. (2018) studied Voltage-gated proton (Hv1) channel function. mutant N264R was evaluated on Gating charge displacement and kinetic analysis. Kinetic analysis of gating currents in the mutant N264R voltage-gated proton channel revealed a complex time course with two peaks and a marked Cole-Moore effect, suggesting at least five states.
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