A peptide segment critical for sodium channel inactivation functions as an inactivation gate in a potassium channel

Neuron. 1993 Nov;11(5):967-74. doi: 10.1016/0896-6273(93)90125-b.

Abstract

The short cytoplasmic peptide segment connecting domains III and IV of voltage-gated sodium channels (III-IV linker) is essential for fast inactivation. To test the functional similarity between the III-IV linker and the potassium channel inactivation particle, we attached the III-IV linker to the amino terminus of a noninactivating potassium channel. This chimeric channel inactivated rapidly and displayed biophysical properties similar to Shaker A-type potassium channels. Recovery from inactivation in the chimeric channels was accelerated by high external potassium, consistent with the idea that potassium ions passing through the channel displaced the III-IV linker inactivation particle. A mutation that completely abolishes fast inactivation in rat brain sodium channels also completely abolished inactivation in the chimera. These results demonstrate that the sodium channel III-IV linker can function as a fast inactivation gate and suggest a functional relationship between the fast inactivation processes of sodium and potassium channels.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Base Sequence
  • Chimera
  • Ion Channel Gating / physiology*
  • Molecular Sequence Data
  • Oligonucleotide Probes / genetics
  • Peptide Fragments / genetics
  • Peptide Fragments / physiology*
  • Potassium Channels / genetics
  • Potassium Channels / physiology*
  • Sodium Channels / genetics
  • Sodium Channels / physiology*

Substances

  • Oligonucleotide Probes
  • Peptide Fragments
  • Potassium Channels
  • Sodium Channels