CDNA Cloning, Heterologous Expression and Characterization of Anti-Neuroexcitation Peptides (ANEPS) of ScorpionButhus martensiiKarsch

. The neurotoxins from scorpion venoms are specifically active on mammals or insects, and divided into two main categories based on their molecular sizes and pharmacological activities. The short-chain toxins consist of 30 to 40 amino acid residues with 3 or 4 disulfide bonds and predominantly act upon potassium or chloride channels, meanwhile the toxins contain 60 to 70 amino acid residues, the long-chain toxins, with 4 disulfide bonds primarily influence sodium channels. These toxins can selectively bind to the corresponding channels on the membrane of excitable cells, impair the initial rapid depolarization phase of the action potential in nerve and muscle, thus result in neurotoxicity. In China, scorpions and their tissues or extracts have been extensively used for treatment of apoplexy, epilepsy, convulsion, facial paralysis, hemiplegia and anti-inflammation etc in traditional Chinese medicine for over thousands of years. Neurotoxins of the scorpion Buthus martensii Karsch (Bmk), a representative species in China and east Asia, have been widely studied in recent fifteen years, including studies on their primary and three-dimensional structures, their cDNA and genomic genes, their physiological and biological functions, and their pharmaceutical properties. We cloned a new anti-neuroexcitation peptide cDNA, expressed and purified it in E. coli and characterized its biological activities. The anti-neuroexcitation peptide is highly homologous to the previously reported anti-epilepsy peptide and shows strong calcium channel enhancement activity. METHOD. According to the previously reported N-terminal amino acid sequence of antiepilepsy peptide (1), two degenerate primers were designed and synthesized. Total RNA was isolated from scorpion telsons and reverse transcribed. RACEs were performed. The PCR product was cloned and sequenced. The putative mature anti-neuroexcitation peptide (ANEP) encoding cDNA was then cloned into pET28a expression plasmid. Recombinant ANEP was purified by His-Bind affinity column. The resulting elute was desalted and concentrated with Amicon stirred ultrafiltration cells (1kDa membrane). Then the protein was further purified on Superdex 30 chromatography and analyzed by SDS-PAGE. Anti-neuroexcitation bioassay was performed essentially according to Xu et al (2) by using thiosemicarbazide induced mice convulsion model. Physiologic saline was used as blank control, sodium phenobarbital (4.0mg/kg) as positive control and recombinant anti-neuroexcitation peptide (2.0mg/kg) as sample respectively. The delayed time on the seizure of convulsive symptom in ANEP group and positive group, in comparison with the control group, was expressed in percentage of the control group and was used as indicator of anti-neuroexcitation biological activity. The cDNA sequence has been submitted to GenBank under accession number AF122003.