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非特异性DNA结合蛋白如何在拥挤环境中寻找靶标。

How nonspecifically DNA-binding proteins search for the target in crowded environments.

作者信息

Ma Yiding, Chen Yuhao, Yu Wancheng, Luo Kaifu

机构信息

CAS Key Laboratory of Soft Matter Chemistry, Collaborative Innovation Center of Chemistry for Energy Materials, and Department of Polymer Science and Engineering, University of Science and Technology of China, Hefei, Anhui 230026, People's Republic of China.

出版信息

J Chem Phys. 2016 Mar 28;144(12):125102. doi: 10.1063/1.4944905.

Abstract

We investigate how a tracer particle searches a target located in DNA modeled by a stiff chain in crowded environments using theoretical analysis and Langevin dynamics simulations. First, we show that the three-dimensional (3D) diffusion coefficient of the tracer only depends on the density of crowders ϕ, while its one-dimensional (1D) diffusion coefficient is affected by not only ϕ but also the nonspecific binding energy ε. With increasing ϕ and ε, no obvious change in the average 3D diffusion time is observed, while the average 1D sliding time apparently increases. We propose theoretically that the 1D sliding of the tracer along the chain could be well captured by the Kramers' law of escaping rather than the Arrhenius law, which is verified directly by the simulations. Finally, the average search time increases monotonously with an increase in ϕ while it has a minimum as a function of ε, which could be understood from the different behaviors of the average number of search rounds with the increasing ϕ or ε. These results provide a deeper understanding of the role of facilitated diffusion in target search of proteins on DNA in vivo.

摘要

我们使用理论分析和朗之万动力学模拟,研究了在拥挤环境中,一个示踪粒子如何在由刚性链模拟的DNA中寻找目标。首先,我们表明示踪粒子的三维(3D)扩散系数仅取决于拥挤剂的密度ϕ,而其一维(1D)扩散系数不仅受ϕ影响,还受非特异性结合能ε的影响。随着ϕ和ε的增加,平均3D扩散时间没有明显变化,而平均1D滑动时间明显增加。我们从理论上提出,示踪粒子沿链的1D滑动可以用克莱默斯逃逸定律很好地描述,而不是阿仑尼乌斯定律,这一点通过模拟得到了直接验证。最后,平均搜索时间随着ϕ的增加而单调增加,而作为ε的函数它有一个最小值,这可以从随着ϕ或ε增加平均搜索轮数的不同行为来理解。这些结果为促进扩散在体内蛋白质在DNA上的目标搜索中的作用提供了更深入的理解。

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