Isolation and characterization of moojenin, an acid-active, anticoagulant metalloproteinase from Bothrops moojeni venom


Autoria(s): de Morais, Nadia C. G.; Neves Mamede, Carla C.; Fonseca, Kelly C.; de Queiroz, Mayara R.; Gomes-Filho, Saulo A.; Santos-Filho, Norival A.; Bordon, Karla de C. F.; Beletti, Marcelo E.; Sampaio, Suely V.; Arantes, Eliane C.; de Oliveira, Fabio
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

04/11/2013

04/11/2013

2012

Resumo

A fibrinogenolytic metalloproteinase from Bothrops moojeni venom, named moojenin, was purified by a combination of ion-exchange chromatography on DEAE-Sephacel and gel filtration on Sephacryl S-300. SDS-PAGE analysis indicated that moojenin consists of a single polypeptide chain and has a molecular mass about 45 kDa. Sequencing of moojenin by Edman degradation revealed the amino acid sequence LGPDIVSPPVCGNELLEV-GEECDCGTPENCQNE, which showed strong identity with many other snake venom metalloproteinases (SVMPs). The enzyme cleaves the A alpha-chain of fibrinogen first, followed by the E beta-chain, and shows no effects on the gamma-chain. Moojenin showed a coagulant activity on bovine plasma about 3.1 fold lower than crude venom. The fibrinogenolytic and coagulant activities of the moojenin were abolished by preincubation with EDTA, 1,10-phenanthroline and beta-mercaptoethanol. Moojenin showed maximum activity at temperatures ranging from 30 to 40 degrees C and its optimal pH was 4.0. Its activity was completely lost at temperatures above 50 degrees C. Moojenin induced necrosis in liver and muscle, evidenced by morphological alterations, but did not cause histological alterations in mouse lungs, kidney or heart. Moojenin rendered the blood uncoagulatable when it was intraperitoneally administered into mice. This metalloproteinase may be of medical interest because of its anticoagulant activity. (C) 2012 Elsevier Ltd. All rights reserved.

Fundacao de Amparo a Pesquisa do Estado de Minas Gerais (FAPEMIG)

Fundacao de Amparo a Pesquisa do Estado de Minas Gerais (FAPEMIG)

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)

Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES)

Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES)

Ministerio de Ciencias e Tecnologia (MCT) of Brazil

Ministerio de Ciencias e Tecnologia (MCT) of Brazil

Identificador

TOXICON, OXFORD, v. 60, n. 7, supl. 1, Part 3, pp. 1251-1258, DEC 1, 2012

0041-0101

http://www.producao.usp.br/handle/BDPI/40810

10.1016/j.toxicon.2012.08.017

http://dx.doi.org/10.1016/j.toxicon.2012.08.017

Idioma(s)

eng

Publicador

PERGAMON-ELSEVIER SCIENCE LTD

OXFORD

Relação

TOXICON

Direitos

closedAccess

Copyright PERGAMON-ELSEVIER SCIENCE LTD

Palavras-Chave #SNAKE VENOM #BOTHROPS MOOJENI #METALLOPROTEINASE #CROTALUS-ATROX VENOM #SNAKE-VENOM #PLATELET-AGGREGATION #BOTHROPS-MOOJENI-(CAISSACA) VENOM #HEMORRHAGIC METALLOPROTEINASE #STRUCTURAL-CHARACTERIZATION #SERINE PROTEINASES #CATROCOLLASTATIN-C #BASIC PROTEINASES #SEQUENCE #PHARMACOLOGY & PHARMACY #TOXICOLOGY
Tipo

article

original article

publishedVersion