IISER-Pune, Dr. Homi Bhaba Road, Pune 411008, India.
Department of Biochemistry and Molecular Pharmacology, NYU Langone Medical Center, New York, New York 10016, USA.
J Chem Phys. 2019 Apr 14;150(14):144908. doi: 10.1063/1.5058214.
We showed in our previous studies that just 3% cross-links (CLs), at special points along the contour of the bacterial DNA, help the DNA-polymer to get organized at micron length scales [T. Agarwal et al., J. Phys.: Condens. Matter 30, 034003 (2018) and T. Agarwal et al., EPL (Europhys. Lett.) 121, 18004 (2018)]. In this work, we investigate how does the release of topological constraints help in the "organization" of the DNA-polymer. Furthermore, we show that the chain compaction induced by the crowded environment in the bacterial cytoplasm contributes to the organization of the DNA-polymer. We model the DNA chain as a flexible bead-spring ring polymer, where each bead represents 1000 base pairs. The specific positions of the CLs have been taken from the experimental contact maps of the bacteria Caulobacter crescentus and Escherichia coli. We introduce different extents of ease of release of topological constraints in our model by systematically changing the diameter of the monomer bead. It varies from the value where chain crossing can occur freely to the value where chain crossing is disallowed. We also study the role of compaction of the chain due to molecular crowders by introducing an "effective" weak Lennard-Jones attraction between the monomers. Using Monte Carlo simulations, we show that the release of topological constraints and the crowding environment play a crucial role to obtain a unique organization of the polymer.
在之前的研究中,我们已经表明,在细菌 DNA 轮廓的特殊点上,只有 3%的交联(CLs)有助于 DNA 聚合酶在微米长度尺度上进行组织化[T. Agarwal 等人,J. Phys.:Condens. Matter 30, 034003 (2018) 和 T. Agarwal 等人,EPL(欧洲物理快报)121, 18004 (2018)]。在这项工作中,我们研究了解拓扑约束的释放如何帮助 DNA 聚合酶进行“组织化”。此外,我们还表明,细菌细胞质中拥挤环境引起的链紧缩有助于 DNA 聚合酶的组织化。我们将 DNA 链建模为一个灵活的珠子-弹簧环聚合物,其中每个珠子代表 1000 个碱基对。CLs 的特定位置取自细菌新月柄杆菌和大肠杆菌的实验接触图谱。我们通过系统改变单体珠的直径,在模型中引入不同程度的拓扑约束释放的容易程度。它的范围从允许链交叉自由发生的珠直径值到不允许链交叉的珠直径值。我们还通过在单体之间引入有效的弱 Lennard-Jones 吸引力来研究链紧缩由于分子拥挤者的作用。通过蒙特卡罗模拟,我们表明拓扑约束的释放和拥挤环境对于获得聚合物的独特组织化起着至关重要的作用。