Department of Chemical and Biological Engineering, Princeton University, Princeton, NJ 08544, USA.
Department of Chemical and Biological Engineering, Princeton University, Princeton, NJ 08544, USA; The Andlinger Center for Energy and the Environment, Princeton University, Princeton, NJ 08544, USA.
Cell. 2018 Nov 29;175(6):1467-1480.e13. doi: 10.1016/j.cell.2018.10.048.
Liquid-liquid phase separation plays a key role in the assembly of diverse intracellular structures. However, the biophysical principles by which phase separation can be precisely localized within subregions of the cell are still largely unclear, particularly for low-abundance proteins. Here, we introduce an oligomerizing biomimetic system, "Corelets," and utilize its rapid and quantitative light-controlled tunability to map full intracellular phase diagrams, which dictate the concentrations at which phase separation occurs and the transition mechanism, in a protein sequence dependent manner. Surprisingly, both experiments and simulations show that while intracellular concentrations may be insufficient for global phase separation, sequestering protein ligands to slowly diffusing nucleation centers can move the cell into a different region of the phase diagram, resulting in localized phase separation. This diffusive capture mechanism liberates the cell from the constraints of global protein abundance and is likely exploited to pattern condensates associated with diverse biological processes. VIDEO ABSTRACT.
液-液相分离在多种细胞内结构的组装中起着关键作用。然而,液-液相分离能够在细胞的亚区域内精确定位的生物物理原理在很大程度上仍不清楚,特别是对于低丰度蛋白质而言。在这里,我们引入了一个聚合仿生系统“Corelets”,并利用其快速和定量的光控可调性,以依赖于蛋白质序列的方式绘制完整的细胞内相图,该相图决定了发生相分离的浓度以及相变机制。令人惊讶的是,实验和模拟都表明,尽管细胞内浓度可能不足以进行全局相分离,但将蛋白质配体隔离到缓慢扩散的成核中心可以将细胞移动到相图的不同区域,从而导致局部相分离。这种扩散捕获机制使细胞摆脱了全局蛋白质丰度的限制,并且可能被用来对与各种生物过程相关的凝聚物进行图案化。视频摘要。