Pesquisa avançada

(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Crystal structure of a phospholipase A(2) from Bothrops asper venom: Insights into a new putative ``myotoxic cluster{''}

Texto completo
Autor(es): Salvador, Guilherme H. M. ; dos Santos, Juliana I. ; Lomonte, Bruno ; Fontes, Marcos R. M.
Tipo de documento: Artigo Científico
Fonte: Biochimie; v. 133, p. 95-102, FEB 2017.
Citações Web of Science: 0
Resumo

Snake venoms from the Viperidae and Elapidae families often have several phospholipases A(2) (PLA(2)s), which may display different functions despite having a similar structural scaffold. These proteins are considered an important target for the development of drugs against local myotoxic damage because they are not efficiently neutralized by conventional serum therapy. PLA(2)s from these venoms are generally divided into two classes: (i) catalytic PLA(2)s (or Asp49-PLA(2)s) and (ii) non-catalytic PLA(2)-like toxins (or Lys49-PLA(2)s). In many Viperidae venoms, a subset of the basic Asp49-PLA2s displays some functional and structural characteristics of PLA(2)-like proteins and group within the same phylogenetic Glade, but their myotoxic mechanism is still largely unknown. In the present study, we have crystallized and solved the structure of myotoxin I (MT-I), a basic myotoxic Asp49-PLA(2) isolated from Bothrops asper venom. The structure presents a dimeric conformation that is compatible with that of previous dimers found for basic myotoxic Asp49-PLA(2)s and Lys49-PLA(2)s and has been confirmed by other biophysical and bioinformatics techniques. This arrangement suggests a possible cooperative action between both monomers to exert myotoxicity via two different sites forming a putative membrane-docking site (MDoS) and a putative membrane disruption site (MDiS). This mechanism would resemble that proposed for Lys49-PLA(2)s, but the sites involved appear to be situated in a different region. Thus, as both sites are close to one another, they form a ``myotoxic cluster{''}, which is also found in two other basic myotoxic Asp49-PLA(2)s from Viperidae venoms. Such arrangement may represent a novel structural strategy for the mechanism of muscle damage exerted by the group of basic, Asp49-PLA(2)s found in viperid snake venoms. (C) 2016 Elsevier B.V. and Societe Francaise de Biochimie et Biologie Moleculaire (SFBBM). All rights reserved. (AU)

Processo FAPESP: 15/24167-7 - Estudos estruturais das proteínas envolvidas na necrose muscular local em acidentes botrópicos
Beneficiário:Guilherme Henrique Marchi Salvador
Linha de fomento: Bolsas no Brasil - Pós-Doutorado
Processo FAPESP: 15/17286-0 - Estudos estruturais e funcionais objetivando compreender o papel de toxinas de venenos de serpentes e de como inibir a sua atividade biológica
Beneficiário:Marcos Roberto de Mattos Fontes
Linha de fomento: Auxílio à Pesquisa - Regular