Contryphan-Vn: a modulator of Ca2+-dependent K+ channels

Biochem Biophys Res Commun. 2003 Mar 28;303(1):238-46. doi: 10.1016/s0006-291x(03)00331-0.

Abstract

Contryphan-Vn is a D-tryptophan-containing disulfide-constrained nonapeptide isolated from the venom of Conus ventricosus, the single Mediterranean cone snail species. The structure of the synthetic Contryphan-Vn has been determined by NMR spectroscopy. Unique among Contryphans, Contryphan-Vn displays the peculiar presence of a Lys-Trp dyad, reminiscent of that observed in several voltage-gated K(+) channel blockers. Electrophysiological experiments carried out on dorsal unpaired median neurons isolated from the cockroach (Periplaneta americana) nerve cord on rat fetal chromaffin cells indicate that Contryphan-Vn affects both voltage-gated and Ca(2+)-dependent K(+) channel activities, with composite and diversified effects in invertebrate and vertebrate systems. Voltage-gated and Ca(2+)-dependent K(+) channels represent the first functional target identified for a conopeptide of the Contryphan family. Furthermore, Contryphan-Vn is the first conopeptide known to modulate the activity of Ca(2+)-dependent K(+) channels.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Calcium / metabolism*
  • Cell Line
  • Cell Line, Transformed
  • Chromaffin Cells / drug effects
  • Chromaffin Cells / metabolism
  • Electrophysiology
  • Humans
  • Magnetic Resonance Spectroscopy
  • Models, Molecular
  • Mollusk Venoms
  • Neurons / drug effects
  • Neurons / metabolism
  • Patch-Clamp Techniques
  • Peptides, Cyclic / metabolism*
  • Peptides, Cyclic / physiology*
  • Potassium Channels / metabolism*
  • Rats
  • Snails / metabolism
  • Time Factors

Substances

  • Mollusk Venoms
  • Peptides, Cyclic
  • Potassium Channels
  • contryphan
  • Calcium