SUPA, School of Physics and Astronomy, University of Edinburgh, Mayfield Road, Edinburgh, EH9 3JZ, United Kingdom.
Phys Rev Lett. 2012 Oct 19;109(16):168103. doi: 10.1103/PhysRevLett.109.168103. Epub 2012 Oct 17.
We present Brownian dynamics simulations of the facilitated diffusion of a protein, modeled as a sphere with a binding site on its surface, along DNA, modeled as a semiflexible polymer. We consider both the effect of DNA organization in three dimensions and of sequence heterogeneity. We find that in a network of DNA loops, which are thought to be present in bacterial DNA, the search process is very sensitive to the spatial location of the target within such loops. Therefore, specific genes might be repressed or promoted by changing the local topology of the genome. On the other hand, sequence heterogeneity creates traps which normally slow down facilitated diffusion. When suitably positioned, though, these traps can, surprisingly, render the search process much more efficient.
我们呈现了布朗动力学模拟,模拟了一个带有表面结合位点的球体的蛋白质沿着 DNA 的易化扩散,DNA 被建模为一个半柔性聚合物。我们考虑了 DNA 在三维空间中的组织以及序列异质性的影响。我们发现,在细菌 DNA 中被认为存在的 DNA 环的网络中,目标在这些环中的空间位置对搜索过程非常敏感。因此,通过改变基因组的局部拓扑结构,特定的基因可能会被抑制或促进。另一方面,序列异质性会产生陷阱,通常会减缓易化扩散。然而,当这些陷阱适当地定位时,它们会出人意料地使搜索过程更加高效。