Marion Sanjin, San Martín Carmen, Šiber Antonio
Center of Excellence for Advanced Materials and Sensing Devices, Institute of Physics, Zagreb, Croatia; Laboratory of Nanoscale Biology, Institute of Bioengineering, School of Engineering, EPFL, Lausanne, Switzerland.
Department of Macromolecular Structures, Centro Nacional de Biotecnología (CNB-CSIC), Madrid, Spain.
Biophys J. 2017 Oct 17;113(8):1643-1653. doi: 10.1016/j.bpj.2017.08.035.
Confined mixtures of a polymer and nonspecifically binding particles (condensers) are studied as models for viruses containing double-stranded DNA (polymer) and condensing proteins (particles). We explore a model in which all interactions between the packed content (polymer and particles) and its confinement are purely repulsive, with only a short-range attraction between the condensers and polymer to simulate binding. In the range of physical parameters applicable to viruses, the model predicts reduction of pressure in the system effected by the condensers, despite the reduction in free volume. Condensers are found to be interspersed throughout the spherical confinement and only partially wrapped in the polymer, which acts as an effective medium for the condenser interactions. Crowding of the viral interior influences the DNA and protein organization, producing a picture inconsistent with a chromatin-like, beads-on-a-string structure. The model predicts an organization of the confined interior compatible with experimental data on unperturbed adenoviruses and polyomaviruses, at the same time providing insight into the role of condensing proteins in the viral infectious cycles of related viral families.
研究了聚合物与非特异性结合颗粒(凝聚剂)的受限混合物,以此作为含有双链DNA(聚合物)和凝聚蛋白(颗粒)的病毒模型。我们探索了一种模型,其中填充内容物(聚合物和颗粒)与其受限环境之间的所有相互作用均为纯排斥力,凝聚剂与聚合物之间仅存在短程吸引力以模拟结合。在适用于病毒的物理参数范围内,该模型预测尽管自由体积减小,但凝聚剂会使系统压力降低。发现凝聚剂散布在整个球形受限环境中,并且仅部分包裹在聚合物中,聚合物充当凝聚剂相互作用的有效介质。病毒内部的拥挤会影响DNA和蛋白质的组织,产生与染色质样的串珠状结构不一致的情况。该模型预测受限内部的组织与未受干扰的腺病毒和多瘤病毒的实验数据相符,同时深入了解了凝聚蛋白在相关病毒家族病毒感染周期中的作用。