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Rev. bras. pesqui. méd. biol ; Braz. j. med. biol. res;41(1): 12-17, Jan. 2008. graf
Article in English | LILACS | ID: lil-469981

ABSTRACT

A serine proteinase with thrombin-like activity was isolated from the venom of the Central American pit viper Bothrops asper. Isolation was performed by a combination of affinity chromatography on aminobenzamidine-Sepharose and ion-exchange chromatography on DEAE-Sepharose. The enzyme accounts for approximately 0.13 percent of the venom dry weight and has a molecular mass of 32 kDa as determined by SDS-PAGE, and of 27 kDa as determined by MALDI-TOF mass spectrometry. Its partial amino acid sequence shows high identity with snake venom serine proteinases and a complete identity with a cDNA clone previously sequenced from this species. The N-terminal sequence of the enzyme is VIGGDECNINEHRSLVVLFXSSGFL CAGTLVQDEWVLTAANCDSKNFQ. The enzyme induces clotting of plasma (minimum coagulant dose = 4.1 µg) and fibrinogen (minimum coagulant dose = 4.2 µg) in vitro, and promotes defibrin(ogen)ation in vivo (minimum defibrin(ogen)ating dose = 1.0 µg). In addition, when injected intravenously in mice at doses of 5 and 10 µg, it induces a series of behavioral changes, i.e., loss of the righting reflex, opisthotonus, and intermittent rotations over the long axis of the body, which closely resemble the `gyroxin-like' effect induced by other thrombin-like enzymes from snake venoms.


Subject(s)
Animals , Mice , Blood Coagulation , Bothrops , Coagulants/isolation & purification , Crotalid Venoms/enzymology , Serine Endopeptidases/isolation & purification , Amino Acid Sequence , Antivenins/therapeutic use , Blood Coagulation/drug effects , Chromatography, Agarose , Chromatography, Ion Exchange , Costa Rica , Coagulants/administration & dosage , Coagulants/pharmacology , Drug Evaluation, Preclinical , Fibrinogen/metabolism , Serine Endopeptidases/chemistry , Serine Endopeptidases/genetics , Serine Endopeptidases/pharmacology , Snake Bites/physiopathology , Thrombin/chemistry
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