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磷脂酶A2超家族(PLA2s)中残基关联网络的保守性分析与分解:对蛇毒毒素结构-功能关系的见解

Conservation analysis and decomposition of residue correlation networks in the phospholipase A2 superfamily (PLA2s): Insights into the structure-function relationships of snake venom toxins.

作者信息

Oliveira Alberto, Bleicher Lucas, Schrago Carlos G, Silva Junior Floriano Paes

机构信息

Fundação Oswaldo Cruz, Instituto Oswaldo Cruz, Laboratório de Bioquímica Experimental e Computacional de Fármacos, 21040-360, Rio de Janeiro, RJ, Brazil.

Universidade Federal de Minas Gerais, Laboratório de Biologia Computacional de Proteínas, 31270-901, Belo Horizonte, MG, Brazil.

出版信息

Toxicon. 2018 May;146:50-60. doi: 10.1016/j.toxicon.2018.03.013. Epub 2018 Mar 30.

Abstract

Phospholipases A2 (PLAs) comprise a superfamily of glycerophospholipids hydrolyzing enzymes present in many organisms in nature, whose catalytic activity was majorly unveiled by analysis of snake venoms. The latter have pharmaceutical and biotechnological interests and can be divided into different functional sub-classes. Our goal was to identify important residues and their relation to the functional and class-specific characteristics in the PLAs family with special emphasis on snake venom PLAs (svPLAs). We identified such residues by conservation analysis and decomposition of residue coevolution networks (DRCN), annotated the results based on the available literature on PLAs, structural analysis and molecular dynamics simulations, and related the results to the phylogenetic distribution of these proteins. A filtered alignment of PLAs revealed 14 highly conserved positions and 3 sets of coevolved residues, which were annotated according to their structural or functional role. These residues are mostly involved in ligand binding and catalysis, calcium-binding, the formation of disulfide bridges and a hydrophobic cluster close to the binding site. An independent validation of the inference of structure-function relationships from our co-evolution analysis on the svPLA2s family was obtained by the analysis of the pattern of selection acting on the Viperidae and Elapidae lineages. Additionally, a molecular dynamics simulation on the Lys49 PLA from Agkistrodon contortrix laticinctus was carried out to further investigate the correlation of the Lys49-Glu69 pair. Our results suggest this configuration can result in a novel conformation where the binding cavity collapses due to the approximation of two loops caused by a strong salt bridge between Glu69 and Arg34. Finally, phylogenetic analysis indicated a correlation between the presence of residues in the coevolved sets found in this analysis and the clade localization. The results provide a guide for important positions in the family of PLAs, and potential new objects of investigation.

摘要

磷脂酶A2(PLAs)是一类甘油磷脂水解酶超家族,存在于自然界中的许多生物体中,其催化活性主要通过对蛇毒的分析得以揭示。蛇毒具有药物和生物技术方面的研究价值,可分为不同的功能亚类。我们的目标是确定PLAs家族中重要的残基及其与功能和类别特异性特征的关系,特别关注蛇毒PLAs(svPLAs)。我们通过保守性分析和残基协同进化网络分解(DRCN)确定了这些残基,根据关于PLAs的现有文献、结构分析和分子动力学模拟对结果进行注释,并将结果与这些蛋白质的系统发育分布相关联。对PLAs的过滤比对揭示了14个高度保守的位置和3组协同进化的残基,根据它们的结构或功能作用进行了注释。这些残基大多参与配体结合与催化、钙结合、二硫键形成以及靠近结合位点的疏水簇形成。通过分析蝰蛇科和眼镜蛇科谱系上的选择模式,对我们关于svPLA2s家族的协同进化分析得出的结构 - 功能关系推断进行了独立验证。此外,对宽带水蛇的Lys49 PLA进行了分子动力学模拟,以进一步研究Lys49-Glu69对的相关性。我们的结果表明,这种构象可导致一种新的构象,其中由于Glu69和Arg34之间的强盐桥导致两个环靠近,结合腔塌陷。最后,系统发育分析表明,本分析中发现的协同进化组中残基的存在与进化枝定位之间存在相关性。这些结果为PLAs家族中的重要位置提供了指导,并为潜在的新研究对象提供了参考。

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