Insights into the role of oligomeric state on the biological activities of crotoxin: crystal structure of a tetrameric phospholipase A(2) formed by two isoforms of crotoxin B from Cratalus durissus terrificus venom
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Data
2008-08-15
Autores
Marchi-Salvador, Daniela P. [UNESP]
Correa, Luiz C. [UNESP]
Magro, Angelo J. [UNESP]
Oliveira, Clayton Z.
Soares, Andreimar M.
Fontes, Marcos R. M. [UNESP]
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Editor
Wiley-Blackwell
Resumo
Crotoxin B (CB or Cdt PLA(2)) is a basic Asp49-PLA(2) found in the venom of Crotalus durissus terrificus and it is one of the subunits that constitute the crotoxin (Cro). This heterodimeric toxin, main component of the C. d. terrificus venom, is completed by an acidic, nontoxic, and nonenzymatic component (crotoxin A, CA or crotapotin), and it is related to important envenomation effects such as neurological disorders, myotoxicity, and renal failure. Although Cro has been crystallized since 1938, no crystal structure of this toxin or its subunits is currently available. In this work, the authors present the crystal structure of novel tetrameric complex formed by two dimers of crotoxin B isoforms (CB1 and CB2). The results suggest that these assemblies are stable in solution and show that Ser1 and Glu92 of CB1 and CB2, respectively, play an important role in the oligomerization. The tetrameric and dimeric conformations resulting from the association of the isoforms may increase the neurotoxicity of the toxin CB by the creation of new binding sites, which could improve the affinity of the molecular complexes to the presynaptic membrane.
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crotoxin B, Asp49-phospholipase A(2), oligomerization, neurotoxic activity, crystal structure, Crotalus durissus terrificus venom
Como citar
Proteins-structure Function and Bioinformatics. Malden: Wiley-blackwell, v. 72, n. 3, p. 883-891, 2008.