Li Lin-Ge, Hou Zhonghuai
Hefei National Laboratory for Physical Sciences at the Microscale & Department of Chemical Physics, University of Science and Technology of China, Hefei 230026, China.
Biophys Rep. 2022 Apr 30;8(2):55-67. doi: 10.52601/bpr.2022.210029.
Liquid-liquid phase separation (LLPS) has proved to be ubiquitous in living cells, forming membraneless organelles (MLOs) and dynamic condensations essential in physiological processes. However, some underlying mechanisms remain challenging to unravel experimentally, making theoretical modeling an indispensable aspect. Here we present a protocol for understanding LLPS from fundamental physics to detailed modeling procedures. The protocol involves a comprehensive physical picture on selecting suitable theoretical approaches, as well as how and what to interpret and resolve from the results. On the particle-based level, we elaborate on coarse-grained simulation procedures from building up models, identifying crucial interactions to running simulations to obtain phase diagrams and other concerned properties. We also outline field-based theories which give the system's density profile to determine phase diagrams and provide dynamic properties by studying the time evolution of density field, enabling us to characterize LLPS systems with larger time and length scales and to further include other nonequilibrium factors such as chemical reactions.
液-液相分离(LLPS)已被证明在活细胞中普遍存在,形成无膜细胞器(MLOs)和生理过程中必不可少的动态凝聚物。然而,一些潜在机制在实验上仍难以阐明,这使得理论建模成为不可或缺的一个方面。在此,我们提出了一个从基础物理到详细建模过程来理解LLPS的方案。该方案涉及一个关于选择合适理论方法的全面物理图景,以及如何从结果中进行解释和解析以及解释和解析什么。在基于粒子的层面上,我们详细阐述了粗粒度模拟过程,从建立模型、识别关键相互作用到运行模拟以获得相图和其他相关性质。我们还概述了基于场的理论,这些理论给出系统的密度分布以确定相图,并通过研究密度场的时间演化提供动态性质,使我们能够表征具有更大时间和长度尺度的LLPS系统,并进一步纳入其他非平衡因素,如化学反应。