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Mass fingerprinting and electrophysiological analysis of the venom from the scorpion Centruroides hirsutipalpus (Scorpiones: Buthidae)
Valdez-Velázquez, Laura L; Olamendi-Portugal, Timoteo; Restano-Cassulini, Rita; Zamudio, Fernando Z; Possani, Lourival D.
Afiliação
  • Valdez-Velázquez, Laura L; Universidad de Colima. Facultad de Ciencias Químicas. Coquimatlan. MX
  • Olamendi-Portugal, Timoteo; Universidad Nacional Autónoma de México. Instituto de Biotecnología. Cuernavaca. MX
  • Restano-Cassulini, Rita; Universidad Nacional Autónoma de México. Instituto de Biotecnología. Cuernavaca. MX
  • Zamudio, Fernando Z; Universidad Nacional Autónoma de México. Instituto de Biotecnología. Cuernavaca. MX
  • Possani, Lourival D; Universidad Nacional Autónoma de México. Instituto de Biotecnología. Cuernavaca. MX
J. venom. anim. toxins incl. trop. dis ; 24: 1-8, 2018. graf, tab
Article em En | LILACS, VETINDEX | ID: biblio-1484752
Biblioteca responsável: BR68.1
Localização: BR68.1
ABSTRACT
Background Centruroides hirsutipalpus, of the family Buthidae, is a scorpion endemic to the Western Pacific region of Mexico. Although medically important, its venom has not yet been studied. Therefore, this communication aims to identify their venom components and possible functions. Methods Fingerprinting mass analysis of the soluble venom from this scorpion was achieved by high-performance liquid chromatography and electrospray mass spectrometry. Furthermore, the soluble venom and its toxic effects were evaluated extensively via electrophysiological assays in HEK cells expressing human voltage-gated Na+ channels (hNav 1.1 to Nav1.6), CHO cells expressing hNav 1.7, potassium channel hERG 1 (Ether-à-go-go-related-gene) and the human K+-channel hKv1.1. Results The separation of soluble venom produced 60 fractions from which 83 distinct components were identified. The molecular mass distribution of these components varies from 340 to 21,120 Da. Most of the peptides have a molecular weight between 7001 and 8000 Da (46% components), a range that usually corresponds to peptides known to affect Na+ channels. Peptides with molecular masses from 3000 to 5000 Da (28% of the components) were identified within the range corresponding to K+-channel blocking toxins. Two peptides were obtained in pure format and completely sequenced one with 29 amino acids, showing sequence similarity to an "orphan peptide" of C. limpidus, and the other with 65 amino acid residues shown to be an arthropod toxin (lethal to crustaceans and toxic to crickets). The electrophysiological results of the whole soluble venom show a beta type modification of the currents of channels Nav1.1, Nav1.2 and Nav1.6. The main effect observed in channels hERG and hKv 1.1 was a reduction of the currents. ..
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Texto completo: 1 Coleções: 01-internacional Base de dados: LILACS / VETINDEX Assunto principal: Venenos de Escorpião / Escorpiões / Impressões Digitais de DNA / Eletrofisiologia Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: J. venom. anim. toxins incl. trop. dis Assunto da revista: TOXICOLOGIA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: México

Texto completo: 1 Coleções: 01-internacional Base de dados: LILACS / VETINDEX Assunto principal: Venenos de Escorpião / Escorpiões / Impressões Digitais de DNA / Eletrofisiologia Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: J. venom. anim. toxins incl. trop. dis Assunto da revista: TOXICOLOGIA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: México