Kim Juin, Jeon Chanil, Jeong Hawoong, Jung Youngkyun, Ha Bae-Yeun
Department of Physics, Korea Advanced Institute of Science and Technology, Daejeon 305-701, Korea.
Soft Matter. 2015 Mar 14;11(10):1877-88. doi: 10.1039/c4sm02198c.
DNA compaction in a bacterial cell is in part carried out by entropic (depletion) forces induced by "free" proteins or crowding particles in the cytoplasm. Indeed, recent in vitro experiments highlight these effects by showing that they alone can condense the E. coli chromosome to its in vivo size. Using molecular dynamics simulations and a theoretical approach, we study how a flexible chain molecule can be compacted by crowding particles with variable sizes in a (cell-like) cylindrical space. Our results show that with smaller crowding agents the compaction occurs at a lower volume fraction but at a larger concentration such that doubling their size is equivalent to increasing their concentration fourfold. Similarly, the effect of polydispersity can be correctly mimicked by adjusting the size of crowders in a homogeneous system. Under different conditions, however, crowding particles can induce chain adsorption onto the cylinder wall, stretching the chain, which would otherwise remain condensed.
细菌细胞中的DNA压缩部分是由细胞质中“游离”蛋白质或拥挤颗粒诱导的熵(耗尽)力来完成的。事实上,最近的体外实验通过表明仅这些力就能将大肠杆菌染色体浓缩到其体内大小,突出了这些效应。我们使用分子动力学模拟和理论方法,研究了在(类似细胞的)圆柱形空间中,具有可变大小的拥挤颗粒如何压缩柔性链分子。我们的结果表明,对于较小的拥挤剂,压缩在较低的体积分数下发生,但在较高的浓度下发生,以至于将它们的大小加倍相当于将它们的浓度增加四倍。同样,通过在均匀系统中调整拥挤剂的大小,可以正确模拟多分散性的影响。然而,在不同条件下,拥挤颗粒会诱导链吸附到圆柱壁上,拉伸链,否则链会保持凝聚状态。