Liu Lin, Luo Kaifu
CAS Key Laboratory of Soft Matter Chemistry, Department of Polymer Science and Engineering, University of Science and Technology of China, Hefei, Anhui Province 230026, People's Republic of China.
J Chem Phys. 2014 Dec 14;141(22):225102. doi: 10.1063/1.4903505.
DNA-binding proteins locate and bind their target sequences positioned on DNA in crowded environments, but the molecular crowding effect on this search process is not clear. Using analytical techniques and Langevin dynamics simulations in two dimensions (2D), we find that the essential physics for facilitated diffusion in 2D search and 3D search is the same. We observe that the average search times have minima at the same optimal nonspecific binding energy for the cases with and without the crowding particle. Moreover, the molecular crowding increases the search time by increasing the average search rounds and the one-dimensional (1D) sliding time of a round, but almost not changing the average 2D diffusion time of a round. In addition, the fraction of 1D sliding time out of the total search time increases with increasing the concentration of crowders. For 2D diffusion, the molecular crowding decreases the jumping length and narrows its distribution due to the cage effect from crowders. These results shed light on the role of facilitated diffusion in DNA targeting kinetics in living cells.
DNA结合蛋白在拥挤环境中定位并结合位于DNA上的目标序列,但其对这一搜索过程的分子拥挤效应尚不清楚。利用二维(2D)分析技术和朗之万动力学模拟,我们发现二维搜索和三维搜索中促进扩散的基本物理原理是相同的。我们观察到,在有和没有拥挤粒子的情况下,平均搜索时间在相同的最佳非特异性结合能量处有最小值。此外,分子拥挤通过增加平均搜索轮数和一轮的一维(1D)滑动时间来增加搜索时间,但几乎不改变一轮的平均二维扩散时间。此外,一维滑动时间在总搜索时间中的比例随着拥挤剂浓度的增加而增加。对于二维扩散,由于拥挤剂的笼效应,分子拥挤会减小跳跃长度并使其分布变窄。这些结果揭示了促进扩散在活细胞DNA靶向动力学中的作用。