Multiple Unfolding Intermediates Obtained by Molecular Dynamic Simulations under Stretching for Immunoglobulin-Binding Domain of Protein G.

Q3 Biochemistry, Genetics and Molecular Biology Open Biochemistry Journal Pub Date : 2009-11-23 DOI:10.2174/1874091X00903010066
Anna V Glyakina, Nikolai K Balabaev, Oxana V Galzitskaya
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引用次数: 6

Abstract

We have studied the mechanical properties of the immunoglobulin-binding domain of protein G at the atomic level under stretching at constant velocity using molecular dynamics simulations. We have found that the unfolding process can occur either in a single step or through intermediate states. Analysis of the trajectories from the molecular dynamic simulations showed that the mechanical unfolding of the immunoglobulin-binding domain of protein G is triggered by the separation of the terminal beta-strands and the order in which the secondary-structure elements break is practically the same in two- and multi-state events and at the different extension velocities studied. It is seen from our analysis of 24 trajectories that the theoretical pathway of mechanical unfolding for the immunoglobulin-binding domain of protein G does not coincide with that proposed in denaturant studies in the absence of force.

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蛋白G免疫球蛋白结合区拉伸分子动力学模拟获得的多个展开中间体。
我们利用分子动力学模拟研究了在等速拉伸下G蛋白免疫球蛋白结合结构域在原子水平上的力学性质。我们发现,展开过程既可以在单一步骤中发生,也可以通过中间状态发生。分子动力学模拟的轨迹分析表明,G蛋白免疫球蛋白结合结构域的机械展开是由末端β链的分离触发的,二级结构元件在两态和多态事件中断裂的顺序几乎是相同的,并且所研究的扩展速度不同。从我们对24条轨迹的分析中可以看出,在没有力的情况下,蛋白质G的免疫球蛋白结合域的机械展开的理论途径与变性研究中提出的途径不一致。
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来源期刊
Open Biochemistry Journal
Open Biochemistry Journal Biochemistry, Genetics and Molecular Biology-Biochemistry, Genetics and Molecular Biology (all)
CiteScore
1.50
自引率
0.00%
发文量
5
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