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Purification and characterization of Heteroscorpine-1 (HS-1) toxin from Heterometrus laoticus scorpion venom

2006; Elsevier BV; Volume: 49; Issue: 1 Linguagem: Inglês

10.1016/j.toxicon.2006.09.003

1879-3150

Nunthawun Uawonggul, Sompong Thammasirirak, Arunrat Chaveerach, Tarinee Arkaravichien, Wandee Bunyatratchata, Wipaporn Ruangjirachuporn, Pornpimol Jearranaiprepame, Takeshi Nakamura, Michiyuki Matsuda, Michimoto Kobayashi, Seisuke Hattori, Sakda Daduang,

Biochemical and Structural Characterization

Crude venom from Thai giant scorpion, Heterometrus laoticus, most commonly found in the northeastern area of Thailand, was evaluated for PD50 (paralytic dose 50) activities from abdominal injection to cricket (Gryllus sp.) and activities against various kinds of microorganisms. It exhibited good results in disc diffusion assay for Bacillus subtilis, Klebsiella pneumoniae, Pseudomonas aeruginosa and Staphylococcus aureus. After purification, toxin showed acceptable results for PD50 determination in entrapped cricket as well as inhibitory activity against B. subtilis, K. pneumoniae, and P. aeruginosa with activities over 300 times higher than that of the crude venom. The purified fraction was showed to contain a single band in SDS-PAGE. MALDI-TOF-MS/MS analysis showed one peak of major protein with 8293 Da. Partial amino acid sequence show high homology to Scorpine—a polypeptide toxin family with potassium channel blocking and defensin activity. The novel toxin was named "Heteroscorpine-1" (HS-1) as the first Scorpine from genus Heterometrus. After full length determination by PCR, HS-1 gene was found to be composed of two exons, separated by an intron. Deduction revealed 95 amino acid residues with 19 residues as the leading sequence. It showed about 80% similarity to Panscorpine and Opiscorpine.