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September 23, 1988Science388 citations

Identification of an Intracellular Peptide Segment Involved in Sodium Channel Inactivation

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PVPeter VassilevTSTodd ScheuerWCWilliam A. Catterall

Key Points

  • This research aims to identify a specific intracellular peptide segment that plays a role in sodium channel inactivation.
  • Tested four site-directed antibodies against a specific peptide segment of the sodium channel alpha subunit.
  • Examined the effects of antibodies on sodium channel inactivation in rat muscle cells at different membrane potentials.
  • Analyzed the correlation between antibody binding and sodium channel activation/inactivation rates.
  • Antibodies against the intracellular segment successfully slowed sodium channel inactivation, with effects blocked by the corresponding peptide antigen.
  • Voltage-dependence observed where antibody effects were greater during depolarization to positive potentials.
  • Antibody binding was quicker at negative potentials, indicating a direct involvement of the peptide in channel inactivation.

Abstract

Antibodies directed against a conserved intracellular segment of the sodium channel alpha subunit slow the inactivation of sodium channels in rat muscle cells. Of four site-directed antibodies tested, only antibodies against the short intracellular segment between homologous transmembrane domains III and IV slowed inactivation, and their effects were blocked by the corresponding peptide antigen. No effects on the voltage dependence of sodium channel activation or of steady-state inactivation were observed, but the rate of onset of the antibody effect and the extent of slowing of inactivation were voltage-dependent. Antibody binding was more rapid at negative potentials, at which sodium channels are not inactivated; antibody-induced slowing of inactivation was greater during depolarizations to more positive membrane potentials. The peptide segment recognized by this antibody appears to participate directly in rapid sodium channel inactivation during large depolarizations and to undergo a conformational change that reduces its accessibility to antibodies as the channel inactivates.

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Cite This Study

Vassilev et al. (1988) studied this question.

synapsesocial.com/papers/6a0b1e91e1320844825d1f20https://doi.org/10.1126/science.2458625
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