首页> 外文期刊>The Journal of Chemical Physics >How nonspecifically DNA-binding proteins search for the target in crowded environments
【24h】

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

机译:非特异性DNA结合蛋白如何在拥挤的环境中搜索目标

获取原文
获取原文并翻译 | 示例
           

摘要

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 phi, while its one-dimensional (1D) diffusion coefficient is affected by not only phi but also the nonspecific binding energy epsilon. With increasing phi and epsilon, 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 phi while it has a minimum as a function of epsilon, which could be understood from the different behaviors of the average number of search rounds with the increasing phi or epsilon. These results provide a deeper understanding of the role of facilitated diffusion in target search of proteins on DNA in vivo. (C) 2016 AIP Publishing LLC.
机译:我们使用理论分析和Langevin动力学模拟研究示踪剂粒子如何在拥挤环境中搜索位于由刚性链建模的DNA中的目标。首先,我们表明示踪剂的三维(3D)扩散系数仅取决于拥挤phi的密度,而其一维(1D)扩散系数不仅受phi的影响,还受非特异性结合能epsilon的影响。随着phi和ε的增加,平均3D扩散时间没有明显变化,而平均1D滑动时间则明显增加。我们从理论上提出,示踪剂沿链的一维滑动可以很好地通过克莱默斯逃逸定律而不是阿伦尼乌斯定律来捕获,而这直接通过仿真进行了验证。最后,平均搜索时间随phi的增加而单调增加,而随ε的变化而具有最小值,这可以从平均搜索轮数随phi或ε的增加的不同行为来理解。这些结果使人们更深入地了解了促进扩散在体内DNA蛋白质目标搜索中的作用。 (C)2016 AIP出版有限责任公司。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号