Identification and characterization of a novel O-superfamily conotoxin from Conus litteratus

J Pept Sci. 2008 Oct;14(10):1077-83. doi: 10.1002/psc.1044.

Abstract

A novel conotoxin named lt6c, an O-superfamily conotoxin, was identified from the cDNA library of venom duct of Conus litteratus. The full-length cDNA contains an open reading frame encoding a predicted 22-residue signal peptide, a 22-residue proregion and a mature peptide of 28 amino acids. The signal peptide sequence of lt6c is highly conserved in O-superfamily conotoxins and the mature peptide consists of six cysteines arranged in the pattern of C-C-CC-C-C that is defined the O-superfamily of conotoxins. The mature peptide fused with thioredoxin, 6-His tag, and a Factor Xa cleavage site was successfully expressed in Escherichia coli. About 12 mg lt6c was purified from 1L culture. Under whole-cell patch-clamp mode, lt6c inhibited sodium currents on adult rat dorsal root ganglion neurons. Therefore, lt6c is a novel O-superfamily conotoxin that is able to block sodium channels.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Cells, Cultured
  • Conotoxins / biosynthesis
  • Conotoxins / chemistry*
  • Conotoxins / genetics
  • Conotoxins / pharmacology
  • Conus Snail / chemistry*
  • Conus Snail / genetics
  • Female
  • Male
  • Molecular Sequence Data
  • Multigene Family
  • Neurons / drug effects
  • Neurons / physiology
  • Rats
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / isolation & purification
  • Recombinant Proteins / pharmacology
  • Sequence Analysis, DNA
  • Sodium Channels / metabolism

Substances

  • Conotoxins
  • Recombinant Proteins
  • Sodium Channels