Paired cysteine substitutions (D60C:R3C) in the bacterial sodium channel NaChBac form a disulfide bond during activation, revealing voltage-dependent formation of an ion pair in real time.
Demonstrates real-time voltage-dependent formation of an ion pair during activation of the voltage sensor, suggesting this interaction catalyzes S4 movement.
The S4 transmembrane segments of voltage-gated ion channels move outward on depolarization, initiating a conformational change that opens the pore, but the mechanism of S4 movement is unresolved. One structural model predicts sequential formation of ion pairs between the S4 gating charges and negative charges in neighboring S2 and S3 transmembrane segments during gating. Here, we show that paired cysteine substitutions for the third gating charge (R3) in S4 and D60 in S2 of the bacterial sodium channel NaChBac form a disulfide bond during activation, thus "locking" the S4 segment and inducing slow inactivation of the channel. Disulfide locking closely followed the kinetics and voltage dependence of activation and was reversed by hyperpolarization. Activation of D60C:R3C channels is favored compared with single cysteine mutants, and mutant cycle analysis revealed strong free-energy coupling between these residues, further supporting interaction of R3 and D60 during gating. Our results demonstrate voltage-dependent formation of an ion pair during activation of the voltage sensor in real time and suggest that this interaction catalyzes S4 movement and channel activation.
DeCaen et al. (2008) studied this question. Paired cysteine substitutions (D60C:R3C) in NaChBac vs. Single cysteine mutants was evaluated on Disulfide bond formation and channel activation kinetics. Paired cysteine substitutions (D60C:R3C) in the bacterial sodium channel NaChBac form a disulfide bond during activation, revealing voltage-dependent formation of an ion pair in real time.