Functional analysis of the alpha-neurotoxin, BmalphaTX14, derived from the Chinese scorpion, Buthus martensii Karsch

Biotechnol Lett. 2006 Nov;28(21):1767-72. doi: 10.1007/s10529-006-9155-y. Epub 2006 Aug 16.

Abstract

The gene encoding the BmalphaTX14 (alpha-neurotoxin TX14) protein, derived from the cDNA library of the Chinese scorpion Buthus martensii Karsch, was expressed in Pichia pastoris. The recombinant protein was purified by metal chelate affinity chromatography and gel filtration chromatography. Using patch-clamp technique, electrophysiological activity of rBmalphaTX14 was identified. In the neurons isolated from mice trigeminal root ganglion, the Na+ current amplitude was reduced by 80% under whole cell patch-clamp recording. There were no apparent modifications to the gating mechanism in the presence of rBmalphaTX14. Although BmalphaTX14 shared a high amino acid sequence similarity with other typical alpha-toxins, it has different effects on neurons. Further electrophysiological analysis suggested that rBmalphaTX14 selectively blocked Na+ channels and is a member of a new group of scorpion toxins.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Chromosomes, Artificial, Yeast
  • Gene Library
  • Mice
  • Molecular Sequence Data
  • Neurotoxins / biosynthesis
  • Neurotoxins / isolation & purification
  • Neurotoxins / pharmacology*
  • Patch-Clamp Techniques
  • Pichia / genetics
  • Pichia / metabolism
  • Recombinant Proteins / biosynthesis
  • Recombinant Proteins / isolation & purification*
  • Recombinant Proteins / pharmacology
  • Scorpion Venoms / chemistry*
  • Scorpions
  • Sequence Homology, Amino Acid
  • Sodium Channel Blockers / isolation & purification*
  • Sodium Channel Blockers / pharmacology
  • Sodium Channels / drug effects*
  • Trigeminal Ganglion / drug effects*

Substances

  • Neurotoxins
  • Recombinant Proteins
  • Scorpion Venoms
  • Sodium Channel Blockers
  • Sodium Channels
  • alpha-neurotoxin TX14, Buthus martensii

Associated data

  • GENBANK/AF156169