TY - JOUR PY - 2012// TI - Comparative proteomic analysis of the venom of the snake taipan, Oxyuranus scutellatus, from Papua New Guinea and Australia: Role of neurotoxic and procoagulant effects in venom toxicity JO - Journal of Proteomics A1 - Herrera, María A1 - Fernandez, Julian A1 - Vargas, Mariángela A1 - Villalta, Mauren A1 - Segura, Alvaro A1 - León, Guillermo A1 - Angulo, Yamileth A1 - Paiva, Owen A1 - Matainaho, Teatulohi A1 - Jensen, Simon D. A1 - Winkel, Kenneth D. A1 - Calvete, Juan J. A1 - Williams, David J. A1 - Gutiérrez, José María SP - 2128 EP - 2140 VL - 75 IS - 7 N2 - The venom proteomes of populations of the highly venomous taipan snake, Oxyuranus scutellatus, from Australia and Papua New Guinea (PNG), were characterized by reverse-phase HPLC fractionation, followed by analysis of chromatographic fractions by SDS-PAGE, N-terminal sequencing, MALDI-TOF mass fingerprinting, and collision-induced dissociation tandem mass spectrometry of tryptic peptides. Proteins belonging to the following eight protein families were identified in the two venoms: phospholipase A(2) (PLA(2)), Kunitz-type inhibitor, metalloproteinase (SVMP), three-finger toxin (3FTx), serine proteinase, cysteine-rich secretory proteins (CRISP), and coagulation factor V-like protein. In addition, C-type lectin/lectin-like protein and venom natriuretic peptide were identified in the venom of specimens from PNG. PLA(2)s comprised more than 65% of the venoms of these two populations. Antivenoms generated against the venoms of these populations showed a pattern of cross-neutralization, corroborating the immunological kinship of these venoms. Toxicity experiments performed in mice suggest that, at low venom doses, neurotoxicity leading to respiratory paralysis represents the predominant mechanism of prey immobilization and death. However, at high doses, such as those injected in natural bites, intravascular thrombosis due to the action of the prothrombin activator may constitute a potent and very rapid mechanism for killing prey.

Language: en

LA - en SN - 1874-3919 UR - http://dx.doi.org/10.1016/j.jprot.2012.01.006 ID - ref1 ER -