TY - JOUR
T1 - Voltage-dependent regulation of modal gating in the rat SkM 1 sodium channel expressed in Xenopus oocytes
AU - Ji, Sen
AU - Sun, Weijing
AU - George, Alfred L.
AU - Horn, Richard
AU - Barchi, Robert L.
N1 - Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.
PY - 1994/10/1
Y1 - 1994/10/1
N2 - The TTX-sensitive rat skeletal muscle sodium channel (rSkM 1) exhibits two modes of inactivation (fast vs slow) when the et subunit is expressed alone in Xenopus oocytes. In this study, two components are found in the voltage dependence of normalized current inactivation, one having a V1/2 in the expected voltage range (--50 mV, IN) and the other with a more hyperpolarized V1/2 (--130 mV, IH) at a holding potential of -90 mV. The IN component is associated with the gating mode having rapid inactivation and recovery from inactivation of the macroscopic current (N-mode), while IH corresponds to the slow inactivation and recovery mode (H-mode). These two components are interconvertible and their relative contribution to the total current varies with the holding potential: IN is favored by hyperpolarization. The interconversion between the two modes is voltage dependent and is well fit to a first-order two-state model with a voltage dependence of e-fold/8.6 mV and a V1/2 of -62 mY. When the rat sodium channel β1-subunit is coinjected with rSkM1, IH is essentially eliminated and the inactivation kinetics of macroscopic current becomes rapid. These two current components and their associated gating modes may represent two conformations of the β subunit, one of which can be stabilized either by hyperpolarization or by binding of the β1 subunit.
AB - The TTX-sensitive rat skeletal muscle sodium channel (rSkM 1) exhibits two modes of inactivation (fast vs slow) when the et subunit is expressed alone in Xenopus oocytes. In this study, two components are found in the voltage dependence of normalized current inactivation, one having a V1/2 in the expected voltage range (--50 mV, IN) and the other with a more hyperpolarized V1/2 (--130 mV, IH) at a holding potential of -90 mV. The IN component is associated with the gating mode having rapid inactivation and recovery from inactivation of the macroscopic current (N-mode), while IH corresponds to the slow inactivation and recovery mode (H-mode). These two components are interconvertible and their relative contribution to the total current varies with the holding potential: IN is favored by hyperpolarization. The interconversion between the two modes is voltage dependent and is well fit to a first-order two-state model with a voltage dependence of e-fold/8.6 mV and a V1/2 of -62 mY. When the rat sodium channel β1-subunit is coinjected with rSkM1, IH is essentially eliminated and the inactivation kinetics of macroscopic current becomes rapid. These two current components and their associated gating modes may represent two conformations of the β subunit, one of which can be stabilized either by hyperpolarization or by binding of the β1 subunit.
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U2 - 10.1085/jgp.104.4.625
DO - 10.1085/jgp.104.4.625
M3 - Article
C2 - 7836935
AN - SCOPUS:0028081370
VL - 104
SP - 625
EP - 643
JO - Journal of General Physiology
JF - Journal of General Physiology
SN - 0022-1295
IS - 4
ER -