The three-dimensional structure of bothropasin, the main hemorrhagic factor from Bothrops jararaca venom: Insights for a new classification of snake venom metalloprotease subgroups


Autoria(s): MUNIZ, Joao R. C.; AMBROSIO, Andre L. B.; SELISTRE-DE-ARAUJO, Heloisa S.; COMINETTI, Marcia R.; MOURA-DA-SILVA, Ana M.; OLIVA, Glaucius; GARRATT, Richard Charles; SOUZA, Dulce H. F.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2008

Resumo

Bothropasin is a 48 kDa hemorrhagic PIII snake venom metalloprotease (SVMP) isolated from Bothrops jararaca, containing disintegrin/cysteine-rich adhesive domains. Here we present the crystal structure of bothropasin complexed with the inhibitor POL647. The catalytic domain consists of a scaffold of two subdomains organized similarly to those described for other SVMPs, including the zinc and calcium-binding sites. The free cysteine residue Cys(189) is located within a hydrophobic core and it is not available for disulfide bonding or other interactions. There is no identifiable secondary structure for the disintegrin domain, but instead it is composed mostly of loops stabilized by seven disulfide bonds and by two calcium ions. The ECD region is in a loop and is structurally related to the RGD region of RGD disintegrins, which are derived from I`ll SVMPs. The ECD motif is stabilized by the Cys(117)_Cys(310) disulfide bond (between the disintegrin and cysteine-rich domains) and by one calcium ion. The side chain of Glu(276) of the ECD motif is exposed to solvent and free to make interactions. In bothropasin, the HVR (hyper-variable region) described for other Pill SVMPs in the cysteine-rich domain, presents a well-conserved sequence with respect to several other Pill members from different species. We propose that this subset be referred to as PIII-HCR (highly conserved region) SVMPs. The differences in the disintegrin-like, cysteine-rich or disintegrin-like cysteine-rich domains may be involved in selecting target binding, which in turn could generate substrate diversity or specificity for the catalytic domain. (C) 2008 Elsevier Ltd. All rights reserved.

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

FAPESP

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

CNPq

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

CAPES (Brazil)

Brazilian Synchrotron Light Laboratory (LNLS)

Laboratorio Nacional de Luz Sincrotron (LNLS), Campinas, Brazil

Polifarma Research Centre, Roma, Italy

Polifarma Research Centre, Roma, Italy[POL647]

Identificador

TOXICON, v.52, n.7, p.807-816, 2008

0041-0101

http://producao.usp.br/handle/BDPI/29984

10.1016/j.toxicon.2008.08.021

http://dx.doi.org/10.1016/j.toxicon.2008.08.021

Idioma(s)

eng

Publicador

PERGAMON-ELSEVIER SCIENCE LTD

Relação

Toxicon

Direitos

restrictedAccess

Copyright PERGAMON-ELSEVIER SCIENCE LTD

Palavras-Chave #Snake venom #Metalloprotease #Disintegrin #X-ray crystallography #Three-dimensional structure #CYSTEINE-RICH DOMAIN #VON-WILLEBRAND-FACTOR #INDUCED PLATELET-AGGREGATION #NECROSIS-FACTOR-ALPHA #DISINTEGRIN-LIKE #CRYSTAL-STRUCTURES #IN-VITRO #CELL-ADHESION #ALTERNAGIN-C #JARARHAGIN #Pharmacology & Pharmacy #Toxicology
Tipo

article

original article

publishedVersion