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含 CaaX 基序的 22 种潜在法尼基转移酶底物的分子动力学分析。

Molecular dynamics analysis of a series of 22 potential farnesyltransferase substrates containing a CaaX-motif.

机构信息

REQUIMTE, Departamento de Química e Bioquímica, Faculdade de Ciências, Universidade do Porto, Rua do Campo Alegre, s/n, 4169-007, Porto, Portugal.

出版信息

J Mol Model. 2013 Feb;19(2):673-88. doi: 10.1007/s00894-012-1590-1. Epub 2012 Sep 26.

Abstract

Protein farnesyltransferase (FTase) is an important target in many research fields, more markedly so in cancer investigation since several proteins known to be involved in human cancer development are thought to serve as substrates for FTase and to require farnesylation for proper biological activity. Several FTase inhibitors (FTIs) have advanced into clinical testing. Nevertheless, despite the progress in the field several functional and mechanistic doubts on the FTase catalytic activity have persisted. This work provides some crucial information on this important enzyme by describing the application of molecular dynamics simulations using specifically designed molecular mechanical parameters for a variety of 22 CaaX peptides known to work as natural substrates or inhibitors for this enzyme. The study involves a comparative analysis of several important molecular aspects, at the mechanistic level, of the behavior of substrates and inhibitors at the dynamic level, including the behavior of the enzyme and peptides, as well as their interaction, together with the effect of the solvent. Properties evaluated include the radial distribution function of the water molecules around the catalytically important zinc metal atom and cysteine sulfur of CaaX, the conformations of the substrate and inhibitor and the corresponding RMSF values, critical hydrogen bonds, and several catalytically relevant distances. These results are discussed in light of recent experimental and computational evidence that provides new insights into the activity of this enzyme.

摘要

蛋白质法尼基转移酶(FTase)是许多研究领域中的一个重要目标,在癌症研究中更为显著,因为已知有几种参与人类癌症发展的蛋白质被认为是 FTase 的底物,并且需要法尼基化才能发挥适当的生物学活性。几种 FTase 抑制剂(FTIs)已进入临床测试。然而,尽管该领域取得了进展,但关于 FTase 催化活性的一些功能和机制上的疑虑仍然存在。这项工作通过使用专门设计的分子力学参数描述了对各种 22 个 CaaX 肽的分子动力学模拟的应用,这些肽已知是该酶的天然底物或抑制剂,从而为这种重要的酶提供了一些关键信息。该研究包括在机制水平上对底物和抑制剂在动态水平上的行为进行了几个重要的分子方面的比较分析,包括酶和肽的行为及其相互作用,以及溶剂的影响。评估的性质包括催化重要锌原子和 CaaX 中半胱氨酸硫的水分子的径向分布函数,底物和抑制剂的构象以及相应的 RMSF 值、关键氢键和几个催化相关的距离。这些结果根据最近的实验和计算证据进行了讨论,这些证据为该酶的活性提供了新的见解。

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