HERG encodes an inwardly-rectifying potassium channel that plays an important role in repolarization of the cardiac action potential. Inward rectification of HERG channels results from rapid and voltage-dependent inactivation gating, combined with very slow activation gating. We asked whether the voltage sensor is implicated in the unusual properties of HERG gating: does the voltage sensor move slowly to account for slow activation and deactivation, or could the voltage sensor move rapidly to account for the rapid kinetics and intrinsic voltage dependence of inactivation? To probe voltage sensor movement, we used a fluorescence technique to examine conformational changes near the positively charged S4 region. Fluorescent probes attached to three different residues on the NH2-terminal end of the S4 region (E518C, E519C, and L520C) reported both fast and slow voltage-dependent changes in fluorescence. The slow changes in fluorescence correlated strongly with activation gating, suggesting that the slow activation gating of HERG results from slow voltage sensor movement. The fast changes in fluorescence showed voltage dependence and kinetics similar to inactivation gating, though these fluorescence signals were not affected by external tetraethylammonium blockade or mutations that alter inactivation. A working model with two types of voltage sensor movement is proposed as a framework for understanding HERG channel gating and the fluorescence signals.
Fast and Slow Voltage Sensor Movements in HERG Potassium Channels
Abbreviations used in this paper: HERG, human ether-à-go-go related gene; TMRM, tetramethylrhodamine maleimide.
In many experiments, fits of the current and the fluorescence reveal that activation is slightly slower than the slow fluorescence and that deactivation is slightly faster than the fluorescence (by up to ∼20%). This discrepancy may be due to a difference in the activation and deactivation kinetics of labeled and unlabeled channels. The fluorescence is reporting changes that occur exclusively in labeled channels, but the current reports the kinetics of both labeled and unlabeled channels. For all three mutants, the g-V relationship of labeled channels is shifted 5–10 mV to the left of the g-V of unlabeled channels, and this slight shift may account for the slight difference between the fluorescence and current kinetics. Over a range of voltages, the steady-state fluorescence-voltage relationship (F-V; Fig. 4, closed circles) and the g-V relationship (Fig. 4, open circles) are nearly identical.
Paula L. Smith, Gary Yellen; Fast and Slow Voltage Sensor Movements in HERG Potassium Channels . J Gen Physiol 1 March 2002; 119 (3): 275–293. doi: https://doi.org/10.1085/jgp.20028534
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