Key result
Swapping S4-S5 and S6 regions transfers hKv2.1 kinetics to hKv1.5, demonstrating interaction drives electromechanical coupling.
Why the study?
The functional role of the interaction between the S4-S5 linker and the cytoplasmic end of S6 in voltage-dependent K(+) channel gating was unclear.
The study elucidates the structural requirements for electromechanical coupling in voltage-dependent potassium channels, specifically the interaction between the S4-S5 linker and the S6 cytoplasmic end.
Answers are grounded in this paper and cite their sources.
No immediate clinical implications; extends molecular models of electromechanical coupling in Kv channels.
Voltage-dependent K(+) channels transfer the voltage sensor movement into gate opening or closure through an electromechanical coupling. To test functionally whether an interaction between the S4-S5 linker (L45) and the cytoplasmic end of S6 (S6(T)) constitutes this coupling, the L45 in hKv1.5 was replaced by corresponding hKv2.1 sequence. This exchange was not tolerated but could be rescued by also swapping S6(T). Exchanging both L45 and S6(T) transferred hKv2.1 kinetics to an hKv1.5 background while preserving the voltage dependence. A one-by-one residue substitution scan of L45 and S6(T) in hKv1.5 further shows that S6(T) needs to be alpha-helical and forms a "crevice" in which residues I422 and T426 of L45 reside. These residues transfer the mechanical energy onto the S6(T) crevice, whereas other residues in S6(T) and L45 that are not involved in the interaction maintain the correct structure of the coupling.
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Labro et al. (2008) studied this question. Sequence swapping of L45 and S6(T) between hKv1.5 and hKv2.1 vs. Wild-type hKv1.5 was evaluated on Channel kinetics and voltage dependence. Exchanging both the S4-S5 linker and the cytoplasmic end of S6 transferred hKv2.1 kinetics to an hKv1.5 background, demonstrating their interaction is required for electromechanical coupling.
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