| Literature DB >> 33620313 |
Carlos Az Bassetto1, João Luis Carvalho-de-Souza1,2, Francisco Bezanilla1,3,4.
Abstract
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 charge-voltage (Q-V) curve that crosses the conductance-voltage (G-V) curve. 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.Entities:
Keywords: S4-S5 segments; W434F; molecular biophysics; neuroscience; pore domain coupling; slow inactivation; structural biology; v-sensing; xenopus
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Year: 2021 PMID: 33620313 PMCID: PMC7943188 DOI: 10.7554/eLife.63077
Source DB: PubMed Journal: Elife ISSN: 2050-084X Impact factor: 8.140