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The data suggest the involvement of a sulfhydryl group in the Na+ channel inactivation gate and its conformational change.
Treatment of murine neuroblastoma N18 cells with N-ethylmaleimide under conditions that favor diminution of membrane potential leads to a 65% increase in the rate of veratridine-stimulated, tetrodotoxin-sensitive Na+ uptake and to a 50% decrease in the concentration of veratridine required for half-maximal stimulation. This modification does not appear to occur in N18 cells having a normal membrane potential of approx. -40 mV. The data are consistent with the involvement of a sulfhydryl group in the Na+ channel inactivation gate and in the conformational change in this gate which results in closing of the channel.
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Panini et al. (1980) studied this question.
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