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包含电荷转移和局域极化效应的锌蛋白模拟。

Zn protein simulations including charge transfer and local polarization effects.

作者信息

Sakharov Dmitri V, Lim Carmay

机构信息

Institute of Biomedical Sciences, Academia Sinica, Taipei 115, Taiwan.

出版信息

J Am Chem Soc. 2005 Apr 6;127(13):4921-9. doi: 10.1021/ja0429115.

Abstract

Nearly half of all proteins contain metal ions, which perform a wide variety of specific functions associated with life processes. However, insights into the local/global, structural and dynamical fluctuations in metalloproteins from molecular dynamics simulations have been hampered by the "conventional" potential energy function (PEF) used in nonmetalloprotein simulations, which does not take into the nonnegligible charge transfer and polarization effects in many metal complexes. Here, we have carried out molecular dynamics simulations of Zn(2+) bound to Cys(-) and/or His(0) in proteins using both the conventional PEF and a novel PEF that accounts for the significant charge transfer and polarization effects in these Zn complexes. Simulations with the conventional PEF yield a nontetrahedral Cys(2)His(2) Zn-binding site and significantly overestimate the experimental Zn-S(Cys(-)) distance. In contrast, simulations with the new PEF accurately reproduce the experimentally observed tetrahedral structures of Cys(2)His(2) and Cys(4) Zn-binding sites in proteins, even when the simulation started from a nontetrahedral Zn(2+) configuration. This suggests that simulations with the new PEF could account for coordinational changes at Zn, which occurs during the folding/unfolding of Zn-finger proteins and certain enzymatic reactions The strategy introduced here can easily be applied to investigate Zn(2+) interacting with protein ligands other than Cys(-) and His(0). It can also be extended to study the interaction of other metals that have significant charge transfer and polarization effects.

摘要

几乎一半的蛋白质都含有金属离子,这些金属离子执行着与生命过程相关的各种各样的特定功能。然而,来自分子动力学模拟的对金属蛋白中局部/全局、结构和动力学波动的深入了解受到了用于非金属蛋白模拟的“传统”势能函数(PEF)的阻碍,该函数没有考虑到许多金属配合物中不可忽视的电荷转移和极化效应。在这里,我们使用传统的PEF和一种新的PEF对蛋白质中与半胱氨酸(Cys⁻)和/或组氨酸(His⁰)结合的锌离子(Zn²⁺)进行了分子动力学模拟,新的PEF考虑了这些锌配合物中显著的电荷转移和极化效应。使用传统PEF的模拟产生了一个非四面体的半胱氨酸(2)组氨酸(2)锌结合位点,并显著高估了实验测得的锌-硫(半胱氨酸⁻)距离。相比之下,使用新的PEF进行的模拟准确地再现了实验观察到的蛋白质中半胱氨酸(2)组氨酸(2)和半胱氨酸(4)锌结合位点的四面体结构,即使模拟从非四面体的锌离子(Zn²⁺)构型开始。这表明使用新的PEF进行的模拟可以解释锌在锌指蛋白折叠/展开和某些酶促反应过程中发生的配位变化。这里介绍的策略可以很容易地应用于研究锌离子(Zn²⁺)与除半胱氨酸(Cys⁻)和组氨酸(His⁰)之外的蛋白质配体的相互作用。它还可以扩展到研究具有显著电荷转移和极化效应的其他金属的相互作用。

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