Department of Chemistry, Louisiana State University, Baton Rouge, Louisiana 70803, United States.
Cornell High Energy Synchrotron Source (CHESS), Cornell University, Ithaca, New York 14853, United States.
Biomacromolecules. 2023 Nov 13;24(11):4771-4782. doi: 10.1021/acs.biomac.3c00545. Epub 2023 Oct 10.
Complex coacervation refers to the liquid-liquid phase separation (LLPS) process occurring between charged macromolecules. The study of complex coacervation is of great interest due to its implications in the formation of membraneless organelles (MLOs) in living cells. However, the impacts of the crowded intracellular environment on the behavior and interactions of biomolecules involved in MLO formation are not fully understood. To address this knowledge gap, we investigated the effects of crowding on a model protein-polymer complex coacervate system. Specifically, we examined the influence of sucrose as a molecular crowder and polyethylene glycol (PEG) as a macromolecular crowder. Our results reveal that the presence of crowders led to the formation of larger coacervate droplets that remained stable over a 25-day period. While sucrose had a minimal effect on the physical properties of the coacervates, PEG led to the formation of coacervates with distinct characteristics, including higher density, increased protein and polymer content, and a more compact internal structure. These differences in coacervate properties can be attributed to the effects of crowders on individual macromolecules, such as the conformation of model polymers, and nonspecific interactions among model protein molecules. Moreover, our results show that sucrose and PEG have different partition behaviors: sucrose was present in both the coacervate and dilute phases, while PEG was observed to be excluded from the coacervate phase. Collectively, our findings provide insights into the understanding of crowding effects on complex coacervation, shedding light on the formation and properties of coacervates in the context of MLOs.
复杂凝聚是指带电荷的大分子之间发生的液-液相分离(LLPS)过程。由于其在无膜细胞器(MLOs)在活细胞中的形成中的意义,复杂凝聚的研究具有重要意义。然而,细胞内拥挤环境对参与 MLO 形成的生物分子的行为和相互作用的影响尚未完全了解。为了解决这一知识空白,我们研究了拥挤对模型蛋白-聚合物复杂凝聚体系的影响。具体来说,我们研究了蔗糖作为分子拥挤剂和聚乙二醇(PEG)作为大分子拥挤剂的影响。研究结果表明,存在拥挤剂会导致凝聚物形成更大的凝聚物液滴,这些液滴在 25 天的时间内保持稳定。虽然蔗糖对凝聚物的物理性质影响不大,但 PEG 导致凝聚物具有独特的特性,包括更高的密度、增加的蛋白质和聚合物含量以及更紧凑的内部结构。凝聚物性质的这些差异可归因于拥挤剂对单个大分子的影响,例如模型聚合物的构象以及模型蛋白分子之间的非特异性相互作用。此外,我们的结果表明,蔗糖和 PEG 具有不同的分配行为:蔗糖存在于凝聚物和稀释相中,而 PEG 被观察到从凝聚物相中排除。总之,我们的研究结果提供了对拥挤效应对复杂凝聚影响的深入了解,阐明了 MLO 背景下凝聚物的形成和性质。