首页> 美国卫生研究院文献>Journal of Biological Physics >Molecular models of the Mojave rattlesnake (Crotalus scutulatus scutulatus) venom metalloproteinases reveal a structural basis for differences in hemorrhagic activities
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Molecular models of the Mojave rattlesnake (Crotalus scutulatus scutulatus) venom metalloproteinases reveal a structural basis for differences in hemorrhagic activities

机译:莫哈韦响尾蛇(Crotalus scutulatus scutulatus)毒液金属蛋白酶的分子模型揭示了出血活性差异的结构基础

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摘要

Rattlesnake venom can differ in composition and in metalloproteinase-associated activities. The molecular basis for this intra-species variation in Crotalus scutulatus scutulatus (Mojave rattlesnake) remains an enigma. To understand the molecular basis for intra-species variation of metalloproteinase-associated activities, we modeled the three-dimensional structures of four metalloproteinases based on the amino acid sequence of four variations of the proteinase domain of the C. s. scutulatus metalloproteinase gene (GP1, GP2, GP3, and GP4). For comparative purposes, we modeled the atrolysin metalloproteinases of C. atrox as well. All molecular models shared the same topology. While the atrolysin metalloproteinase molecular models contained highly conserved substrate binding sites, the Mojave rattlesnake metalloproteinases showed higher structural divergence when superimposed onto each other. The highest structural divergence among the four C. s. scutulatus molecular models was located at the northern cleft wall and the S’1-pocket of the substrate binding site, molecular regions that modulate substrate selectivity. Molecular dynamics and field potential maps for each C. s. scutulatus metalloproteinase model demonstrated that the non-hemorrhagic metalloproteinases (GP2 and GP3) contain highly basic molecular and field potential surfaces while the hemorrhagic metalloproteinases GP1 and atrolysin C showed extensive acidic field potential maps and shallow but less dynamic active site pockets. Hence, differences in the spatial arrangement of the northern cleft wall, the S’1-pocket, and the physico-chemical environment surrounding the catalytic site contribute to differences in metalloproteinase activities in the Mojave rattlesnake. Our results provide a structural basis for variation of metalloproteinase-associated activities in the rattlesnake venom of the Mojave rattlesnake.>Electronic Supplementary MaterialThe online version of this article (doi:10.1007/s10867-013-9339-3) contains supplementary material, which is available to authorized users.
机译:响尾蛇毒液的成分和与金属蛋白酶相关的活性可能不同。克氏tal(Mojave rattlesnake)的种内变异的分子基础仍然是一个谜。为了了解金属蛋白酶相关活性的种内变异的分子基础,我们基于梭菌蛋白酶结构域的四个变异的氨基酸序列,对四种金属蛋白酶的三维结构进行了建模。盾cut金属蛋白酶基因(GP1,GP2,GP3和GP4)。为了进行比较,我们还对C. atrox的atrolysin金属蛋白酶进行了建模。所有分子模型共享相同的拓扑。尽管Atrolysin金属蛋白酶分子模型包含高度保守的底物结合位点,但Mojave响尾蛇金属蛋白酶在彼此重叠时显示出更高的结构差异。四个C.s中最高的结构差异。盾cut分子模型位于北裂壁和底物结合位点的S’1口袋,即调节底物选择性的分子区域。每个C.s.的分子动力学和场势图。 scutulatus金属蛋白酶模型表明,非出血性金属蛋白酶(GP2和GP3)具有高度碱性的分子和电场势能表面,而出血性金属蛋白酶GP1和Atrolysin C表现出广泛的酸性电场势图和较浅但较不活跃的活性位点。因此,北裂壁,S’1口袋和催化位点周围的物理化学环境的空间分布差异,导致莫哈韦响尾蛇中金属蛋白酶活性的差异。我们的研究结果为改变莫哈韦响尾蛇响尾蛇毒液中金属蛋白酶相关活性的变化提供了结构基础。>电子补充材料本文的在线版本(doi:10.1007 / s10867-013-9339-3 )包含补充材料,授权用户可以使用。

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