Ca(2+)-dependent inactivation of a cloned cardiac Ca2+ channel alpha 1 subunit (alpha 1C) expressed in Xenopus oocytes

Biophys J. 1994 Jun;66(6):1895-903. doi: 10.1016/S0006-3495(94)80983-X.

Abstract

The alpha 1 subunit of cardiac Ca2+ channel, expressed alone or coexpressed with the corresponding beta subunit in Xenopus laevis oocytes, elicits rapidly inactivating Ca2+ currents. The inactivation has the following properties: 1) It is practically absent in external Ba2+; 2) it increases with Ca2+ current amplitudes; 3) it is faster at more negative potentials for comparable Ca2+ current amplitudes; 4) it is independent of channel density; and 5) it does not require the beta subunit. These findings indicate that the Ca2+ binding site responsible for inactivation is encoded in the alpha 1 subunit and suggest that it is located near the inner channel mouth but outside the membrane electric field.

Publication types

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

MeSH terms

  • Alternative Splicing
  • Animals
  • Barium / pharmacology
  • Calcium / pharmacology*
  • Calcium Channel Blockers / pharmacology*
  • Calcium Channels / biosynthesis
  • Calcium Channels / physiology*
  • Cloning, Molecular
  • Egtazic Acid / analogs & derivatives
  • Egtazic Acid / pharmacology
  • Electric Conductivity / drug effects
  • Female
  • In Vitro Techniques
  • Macromolecular Substances
  • Membrane Potentials / drug effects
  • Membrane Potentials / physiology
  • Myocardium / metabolism*
  • Oocytes / drug effects
  • Oocytes / physiology*
  • Recombinant Proteins / biosynthesis
  • Recombinant Proteins / metabolism
  • Xenopus laevis

Substances

  • Calcium Channel Blockers
  • Calcium Channels
  • Macromolecular Substances
  • Recombinant Proteins
  • Barium
  • Egtazic Acid
  • 1,2-bis(2-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid
  • Calcium