Immobilizing the Moving Parts of Voltage-Gated Ion Channels
Open Access
- 28 August 2000
- journal article
- research article
- Published by Rockefeller University Press in The Journal of general physiology
- Vol. 116 (3) , 461-476
- https://doi.org/10.1085/jgp.116.3.461
Abstract
Voltage-gated ion channels have at least two classes of moving parts, voltage sensors that respond to changes in the transmembrane potential and gates that create or deny permeant ions access to the conduction pathway. To explore the coupling between voltage sensors and gates, we have systematically immobilized each using a bifunctional photoactivatable cross-linker, benzophenone-4-carboxamidocysteine methanethiosulfonate, that can be tethered to cysteines introduced into the channel protein by mutagenesis. To validate the method, we first tested it on the inactivation gate of the sodium channel. The benzophenone-labeled inactivation gate of the sodium channel can be trapped selectively either in an open or closed state by ultraviolet irradiation at either a hyperpolarized or depolarized voltage, respectively. To verify that ultraviolet light can immobilize S4 segments, we examined its relative effects on ionic and gating currents in Shaker potassium channels, labeled at residue 359 at the extracellular end of the S4 segment. As predicted by the tetrameric stoichiometry of these potassium channels, ultraviolet irradiation reduces ionic current by approximately the fourth power of the gating current reduction, suggesting little cooperativity between the movements of individual S4 segments. Photocross-linking occurs preferably at hyperpolarized voltages after labeling residue 359, suggesting that depolarization moves the benzophenone adduct out of a restricted environment. Immobilization of the S4 segment of the second domain of sodium channels prevents channels from opening. By contrast, photocross-linking the S4 segment of the fourth domain of the sodium channel has effects on both activation and inactivation. Our results indicate that specific voltage sensors of the sodium channel play unique roles in gating, and suggest that movement of one voltage sensor, the S4 segment of domain 4, is at least a two-step process, each step coupled to a different gate.Keywords
This publication has 66 references indexed in Scilit:
- The Role of the Putative Inactivation Lid in Sodium Channel Gating Current ImmobilizationThe Journal of general physiology, 2000
- A Piston Model for Transmembrane Signaling of the Aspartate ReceptorScience, 1999
- The screw–helical voltage gating of ion channelsProceedings Of The Royal Society B-Biological Sciences, 1999
- Interactions between a Pore-Blocking Peptide and the Voltage Sensor of the Sodium Channel: An Electrostatic Approach to Channel GeometryNeuron, 1996
- Evidence for voltage-dependent S4 movement in sodium channelsNeuron, 1995
- Identification of a translocated protein segment in a voltage-dependent channelNature, 1994
- Dynamic Transitions of the Transmembrane Domain of Diphtheria Toxin: Disulfide Trapping and Fluorescence Proximity StudiesBiochemistry, 1994
- Sodium channel mutations in paramyotonia congenita uncouple inactivation from activationNeuron, 1994
- Evidence for cooperative interactions in potassium channel gatingNature, 1992
- Gating of Na channels. Inactivation modifiers discriminate among models.The Journal of general physiology, 1987