Proceedings of the National Academy of Sciences · 1997 · 312 citations · 40 references
Natural SciencesCell BiologyMolecular BiologyCell SignalingElectrophysiologyIon Channel BiophysicsChannel StructureIon Channel PhysiologyIon Channel RegulationIon ChannelsMembrane ElectrophysiologyPotassium Channel BiophysicsChannelsTransient ExpressionTransmembrane DomainsTransmembrane ProteinsVoltage-dependent Ion ChannelsVoltage-gated ChannelsVoltage-gated Ion ChannelsVoltage-gated Potassium Channels
Large conductance voltage- and Ca2+-dependent K+ (MaxiK) channels show sequence similarities to voltage-gated ion channels. They have a homologous S1-S6 region, but are unique at the N and C termini. At the C terminus, MaxiK channels have four additional hydrophobic regions (S7-S10) of unknown topology. At the N terminus, we have recently proposed a new model where MaxiK channels have an additional transmembrane region (S0) that confers beta subunit regulation. Using transient expression of epitope tagged MaxiK channels, in vitro translation, functional, and "in vivo" reconstitution assays, we now show that MaxiK channels have seven transmembrane segments (S0-S6) at the N terminus and a S1-S6 region that folds in a similar way as in voltage-gated ion channels. Further, our results indicate that hydrophobic segments S9-S10 in the C terminus are cytoplasmic and unequivocally demonstrate that S0 forms an additional transmembrane segment leading to an exoplasmic N terminus.
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