Chattaraj Aniruddha, Baltaci Zeynep, Mayer Bruce J, Loew Leslie M, Ditlev Jonathon A
R. D. Berlin Center for Cell Analysis and Modeling, University of Connecticut School of Medicine, Farmington, Connecticut, United States of America.
Program in Molecular Medicine, Hospital for Sick Children, Toronto, Ontario, Canada.
bioRxiv. 2024 Jan 26:2024.01.23.576869. doi: 10.1101/2024.01.23.576869.
Cellular condensates often consist of 10s to 100s of distinct interacting molecular species. Because of the complexity of these interactions, predicting the point at which they will undergo phase separation into discrete compartments is daunting. Using experiments and computation, we therefore studied a simple model system consisting of 2 proteins, polySH3 and polyPRM, designed for pentavalent heterotypic binding. We tested whether the peak solubility product, the product of dilute phase monomer concentrations, is a predictive parameter for the onset of phase separation. Titrating up equal total concentrations of each component showed that the maximum solubility product does approximately coincide with the threshold for phase separation in both the experiments and models. However, we found that measurements of dilute phase concentration include contributions from small oligomers, not just monomers; therefore, a quantitative comparison of the experiments and models required inclusion of small oligomers in the model analysis. We also examined full phase diagrams where the model results were almost symmetric along the diagonal, but the experimental results were highly asymmetric. This led us to perform dynamic light scattering experiments, where we discovered a weak homotypic interaction for polyPRM; when this was added to the computational model, it was able to recapitulate the experimentally observed asymmetry. Thus, comparing experiments to simulation reveals that the solubility product can be predictive of phase separation, even if small oligomers and low affinity homotypic interactions preclude experimental measurement of monomer concentration.
细胞凝聚物通常由数十到数百种不同的相互作用分子组成。由于这些相互作用的复杂性,预测它们何时会发生相分离形成离散区室是一项艰巨的任务。因此,我们通过实验和计算研究了一个简单的模型系统,该系统由两种蛋白质组成,即多SH3和多PRM,设计用于五价异型结合。我们测试了峰值溶解度积(稀相单体浓度的乘积)是否是相分离起始的预测参数。滴定每种组分相等的总浓度表明,在实验和模型中,最大溶解度积确实大致与相分离阈值一致。然而,我们发现稀相浓度的测量包括来自小寡聚物的贡献,而不仅仅是单体;因此,实验和模型的定量比较需要在模型分析中纳入小寡聚物。我们还研究了完整的相图,其中模型结果沿对角线几乎对称,但实验结果高度不对称。这促使我们进行动态光散射实验,在实验中我们发现多PRM存在弱的同型相互作用;当将其添加到计算模型中时,它能够重现实验观察到的不对称性。因此,将实验与模拟进行比较表明,即使小寡聚物和低亲和力同型相互作用妨碍了单体浓度的实验测量,溶解度积仍可预测相分离。