Crystallographic portrayal of different conformational states of a Lys49 phospholipase A2 homologue: Insights into structural determinants for myotoxicity and dimeric configuration

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Data

2012-10-01

Autores

Ullah, A. [UNESP]
Souza, T. A C B
Betzel, C.
Murakami, M. T.
Arni, R. K. [UNESP]

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Resumo

Catalytically inactive phospholipase A2 (PLA2) homologues play key roles in the pathogenesis induced by snake envenomation, causing extensive tissue damage via a mechanism still unknown. Although, the amino acid residues directly involved in catalysis are conserved, the substitution of Asp49 by Arg/Lys/Gln or Ser prevents the binding of the essential calcium ion and hence these proteins are incapable of hydrolyzing phospholipids. In this work, the crystal structure of a Lys49-PLA2 homologue from Bothrops brazili (MTX-II) was solved in two conformational states: (a) native, with Lys49 singly coordinated by the backbone oxygen atom of Val31 and (b) complexed with tetraethylene glycol (TTEG). Interestingly, the TTEG molecule was observed in two different coordination cages depending on the orientation of the nominal calcium-binding loop and of the residue Lys49. These structural observations indicate a direct role for the residue Lys49 in the functioning of a catalytically inactive PLA2 homologue suggesting a contribution of the active site-like region in the expression of pharmacological effects such as myotoxicity and edema formation. Despite the several crystal structures of Lys49-PLA2 homologues already determined, their biological assembly remains controversial with two possible conformations. The extended dimer with the hydrophobic channel exposed to the solvent and the compact dimer in which the active site-like region is occluded by the dimeric interface. In the MTX-II crystal packing analysis was found only the extended dimer as a possible stable quaternary arrangement. © 2012 Elsevier B.V.

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Bothrops brazili, Conformational states, Lys49 phospholipase A2 homologue, Oligomerization, Tetraethylene glycol, dimer, glycol, lysine, myotoxin ii, phospholipase A2, snake venom, tetraethylene glycol, unclassified drug, Bothrops, calcium binding, catalysis, complex formation, crystal structure, crystallography, enzyme conformation, myotoxicity, oligomerization, protein assembly, protein expression, solvent effect, structure analysis, toxicity, Animals, Catalytic Domain, Ethylene Glycols, Ligands, Models, Molecular, Mutant Proteins, Phospholipases A2, Protein Conformation, Protein Multimerization, Protein Structure, Secondary

Como citar

International Journal of Biological Macromolecules, v. 51, n. 3, p. 209-214, 2012.