Repulsion between tetraethylammonium ions in cloned voltage-gated potassium channels

Neuron. 1992 May;8(5):975-82. doi: 10.1016/0896-6273(92)90212-v.

Abstract

Tetraethylammonium ion (TEA+) blocks voltage-gated K+ channels by acting at two sites located at opposite ends of the aqueous pore. This allowed us to test two predictions made by models of ion permeation, namely that K+ channels can be simultaneously occupied by multiple ions and that the ions repel each other. We show that externally applied TEA+ antagonize block by internal TEA+ and vice versa. The antagonism is less than predicted for competitive binding, hence TEA+ may occupy both sites simultaneously. External TEA+ and internal TEA+ reduce each others affinity 4- to 5-fold. In addition, K+ antagonizes block by TEA+ at the opposite side of the membrane, and external TEA+ antagonizes is block by internal Ba2+. The antagonism between ions applied at opposite sides of the membrane may be common to all cations binding to K+ channels.

Publication types

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

MeSH terms

  • Animals
  • Barium / pharmacology
  • Binding, Competitive
  • Cations
  • Electrophysiology
  • Female
  • Oocytes / physiology
  • Potassium / pharmacology
  • Potassium Channels / drug effects
  • Potassium Channels / genetics
  • Potassium Channels / physiology*
  • RNA, Messenger / genetics
  • Tetraethylammonium
  • Tetraethylammonium Compounds / antagonists & inhibitors
  • Tetraethylammonium Compounds / metabolism
  • Tetraethylammonium Compounds / pharmacology*
  • Transfection
  • Xenopus laevis

Substances

  • Cations
  • Potassium Channels
  • RNA, Messenger
  • Tetraethylammonium Compounds
  • Barium
  • Tetraethylammonium
  • Potassium