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Compared chemical properties of dermonecrotic and lethal toxins from spiders of the genusLoxosceles (Araneae)
Authors:Katia C Barbaro  Marcelo V Sousa  Lauro Morhy  Vera R D Eickstedt  Ivan Mota
Institution:1. Laboratório de Imunopatologia, Instituto Butantan, 05503-900, S?o Paulo SP, Brazil
2. Centro Brasileiro de Sequenciamento de Proteínas, Departamento de Biologia Celular, Universidade de Brasília, 70910-900, Brasília DF, Brazil
3. Laboratório de Artrópodos Pe?onhentos, Instituto Butantan, 05503-900, S?o Paulo SP, Brazil
Abstract:Loxosceles spider venom usually causes a typical dermonecrotic lesion in bitten patients, but it may also cause systemic effects that may be lethal. Gel filtration on Sephadex G-100 ofLoxosceles gaucho, L. laeta, orL. intermedia spider venoms resulted in three fractions (A, containing higher molecular mass components, B containing intermediate molecular mass components, and C with lower molecular mass components). The dermonecrotic and lethal activities were detected exclusively in fraction A of all three species. Analysis by SDS-PAGE showed that the major protein contained in fraction A has molecular weight approximately 35 kDa inL. gaucho andL. intermedia, but 32 kDa inL. laeta venom. These toxins were isolated from venoms ofL. gaucho, L. laeta, andL. intermedia by SDS-PAGE followed by blotting to PVDF membrane and sequencing. A database search showed a high level of identity between each toxin and a fragment of theL. reclusa (North American spider) toxin. A multiple sequence alignment of theLoxosceles toxins showed many common identical residues in their N-terminal sequences. Identities ranged from 50.0% (L. gaucho andL. reclusa) to 61.1% (L. intermedia andL. reclusa). The purified toxins were also submitted to capillary electrophoresis peptide mapping afterin situ partial hydrolysis of the blotted samples. The results obtained suggest thatL. intermedia protein is more similar toL. laeta toxin thanL. gaucho toxin and revealed a smaller homology betweenL. intermedia andL gaucho. Altogether these findings suggest that the toxins responsible for most important activities of venoms ofLoxosceles species have a molecular mass of 32–35 kDa and are probably homologous proteins.
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