Department of Biophysics and Howard Hughes Medical Institute, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
J Mol Biol. 2018 Nov 2;430(23):4666-4684. doi: 10.1016/j.jmb.2018.08.003. Epub 2018 Aug 9.
Biomolecular condensates are two- and three-dimensional compartments in eukaryotic cells that concentrate specific collections of molecules without an encapsulating membrane. Many condensates behave as dynamic liquids and appear to form through liquid-liquid phase separation driven by weak, multivalent interactions between macromolecules. In this review, we discuss current models and data regarding the control of condensate composition, and we describe our current understanding of the composition of representative condensates including PML nuclear bodies, P-bodies, stress granules, the nucleolus, and two-dimensional membrane localized LAT and nephrin clusters. Specific interactions, such as interactions between modular binding domains, weaker interactions between intrinsically disorder regions and nucleic acid base pairing, and nonspecific interactions, such as electrostatic interactions and hydrophobic interactions, influence condensate composition. Understanding how specific condensate composition is determined is essential to understanding condensates as biochemical entities and ultimately discerning their cellular and organismic functions.
生物分子凝聚物是真核细胞中的二维和三维隔室,其中浓缩特定的分子集合,而没有包膜。许多凝聚物表现为动态液体,并似乎通过大分子之间的弱多价相互作用驱动的液-液相分离而形成。在这篇综述中,我们讨论了关于凝聚物组成控制的当前模型和数据,并描述了我们对代表性凝聚物的组成的当前理解,包括 PML 核体、P 体、应激颗粒、核仁以及二维膜定位的 LAT 和nephrin 簇。特定的相互作用,如模块化结合域之间的相互作用、固有无序区与核酸碱基配对之间的较弱相互作用以及非特异性相互作用,如静电相互作用和疏水相互作用,影响凝聚物的组成。了解特定凝聚物组成是如何确定的,对于理解凝聚物作为生化实体以及最终辨别其细胞和机体功能至关重要。