Key result
Epilepsy-causing mutations R198Q and R214W alter KCNQ2 channel opening through distinct mechanisms, with R198Q shifting S4 movement and R214W changing the voltage sensor-to-pore coupling.
Why the study?
The impact of mutations on KCNQ2 channel function remains poorly defined due to limited understanding of voltage-sensing mechanisms that trigger channel gating.
The study reveals that KCNQ2 channel opening does not require multiple voltage-sensor movements and demonstrates how epilepsy-causing mutations like R214W uncouple voltage sensor movement from pore opening.
New KCNQ2 voltage-sensing data may clarify mutation effects; leaves open clinical translation for epileptic encephalopathies.
Neuronal KCNQ channels mediate the muscarine-regulated M-current, a key regulator of membrane excitability in the central and peripheral nervous systems. Mutations in KCNQ2 channels cause severe neurodevelopmental disorders, including epileptic encephalopathies. However, the impact that mutations have on channel function remain poorly defined, largely because of our limited understanding of the voltage sensing mechanisms that trigger channel gating. Here, we present measurements of voltage sensor movements in wt-KCNQ2 and channels bearing epilepsy-causing mutations using mutagenesis, cysteine accessibility, and voltage clamp fluorometry (VCF). Cysteine modification reveals that a stretch of 8-9 amino acids in the S4 become exposed upon opening of KCNQ2 channels. VCF shows that the voltage dependence and kinetics of S4 movement and channel opening/closing closely correlate, suggesting an activation scheme in which channel opening does not require multiple voltage-sensor movements. VCF and kinetic modeling reveal different mechanisms by which epilepsy-causing mutations affect KCNQ2 channel voltage-dependent gating. This study provides insight into KCNQ2 channel function, which will aid in uncovering the mechanisms underlying channelopathies.
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Edmond et al. (2022) studied Epilepsy (KCNQ2 channelopathies). KCNQ2 mutations R198Q and R214W vs. Wild-type KCNQ2 was evaluated on Voltage sensor (S4) movement and channel opening. Epilepsy-causing mutations R198Q and R214W alter KCNQ2 channel opening through distinct mechanisms, with R198Q shifting S4 movement and R214W changing the voltage sensor-to-pore coupling.
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