Published February 23, 2021 | Version v1
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Molecular basis for functional connectivity between the voltage sensor and the selectivity filter gate in Shaker K+ channels

Description

In Shaker K+ channels, the S4-S5 linker couples the voltage sensor (VSD) and pore domain (PD). Another coupling mechanism is revealed using two W434F-containing channels: L361R:W434F and L366H:W434F. In L361R:W434F, W434F affects the L361R VSD seen as a shallower Q-V curve that crosses the G-V. In L366H:W434F, L366H relieves the W434F effect converting a non-conductive channel in a conductive one. We report a chain of residues connecting the VSD (S4) to the selectivity filter (SF) in the PD of an adjacent subunit as the molecular basis for voltage-sensor selectivity filter gate (VS-SF) coupling. Single alanine substitutions in this region (L409A, S411A, S412A or F433A) are enough to disrupt the VS-SF coupling, shown by the absence of Q-V and G-V crossing in L361R:W434F mutant and by the lack of ionic conduction in the L366H:W434F mutant. This residue chain defines a new coupling between the VSD and the PD in voltage-gated channels.

Data availability

All data generated or analysed during this study are included in the manuscript and supporting files.

The following previously published data sets were used:

Carvalho-de-Souza JL Bezanilla F (2018) Fig 2B ID JGP. Nonsensing residues in S3-S4 linker's C terminus affect the voltage sensor set point in K+ channels. https://rupress.org/jgp/article/150/2/307/43720/Nonsensing-residues-in-S3-S4-linker-s-C-terminus

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Additional details

Identifiers

DOI
10.7554/eLife.63077
Other
oai:uchicago.tind.io:9914

Funding

National Institutes of Health
R01-GM030376

UChicago Information

Division(s)
Biological Sciences Division
Department(s)
Biochemistry and Molecular Biology
Center(s) or Institute(s)
Institute for Biophysical Dynamics