首页> 外文期刊>Journal of the American Chemical Society >Interplay between Short-Range Attraction and Long-Range Repulsion Controls Reentrant Liquid Condensation of Ribonucleoprotein-RNA Complexes
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Interplay between Short-Range Attraction and Long-Range Repulsion Controls Reentrant Liquid Condensation of Ribonucleoprotein-RNA Complexes

机译:短程吸引力和长程排斥之间的相互作用控制核糖核糖核酸-RNA复合物的折返液体冷凝。

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In eukaryotic cells, ribonucleoproteins (RNPs) form mesoscale condensates by liquid-liquid phase separation that play essential roles in subcellular dynamic compartmentalization. The formation and dissolution of many RNP condensates are finely dependent on the RNA-to-RNP ratio, giving rise to a windowlike phase separation behavior. This is commonly referred to as reentrant liquid condensation (RLC). Here, using ribonucleoprotein-inspired polypeptides with low-complexity RNA-binding sequences as well as an archetypal disordered RNP, fused in sarcoma, as model systems, we investigate the molecular driving forces underlying this nonmonotonous phase transition. We show that an interplay between short-range cation-Z attractions and long-range electrostatic forces governs the heterotypic RLC behavior of RNP-RNA complexes. Short-range attractions, which can be encoded by both polypeptide chain primary sequence and nucleic acid base sequence, control the two-phase coexistence regime, regulate material properties of polypeptide-RNA condensates, and oppose condensate reentrant dissolution. In the presence of excess RNA, a competition between short-range attraction and long-range electrostatic repulsion drives the formation of a colloidlike cluster phase. With increasing short-range attraction, the fluid dynamics of the cluster phase is arrested, leading to the formation of a colloidal gel. Our results reveal that phase behavior, supramolecular organization, and material states of RNP-RNA assemblies are controlled by a dynamic interplay between molecular interactions at different length scales.
机译:在真核细胞中,核糖核蛋白(RNP)通过液-液相分离形成中尺度的缩合物,在亚细胞动态区室化中起重要作用。许多RNP冷凝物的形成和溶解都取决于RNA与RNP的比例,从而产生窗口状的相分离行为。这通常称为折返液体冷凝(RLC)。在这里,使用具有低复杂性RNA结合序列的核糖核酸启发的多肽以及融合在肉瘤中的原型无序RNP作为模型系统,我们研究了这种非单调相变的分子驱动力。我们显示,短距离阳离子Z吸引力和远程静电力之间的相互作用决定了RNP-RNA复合物的异型RLC行为。可由多肽链一级序列和核酸碱基序列编码的短程引力,控制两相共存机制,调节多肽-RNA冷凝物的物质特性,并反对冷凝物折返溶解。在存在过量RNA的情况下,短距离吸引与长距离静电排斥之间的竞争推动了胶体状簇相的形成。随着短程吸引的增加,簇相的流体动力学被阻止,导致形成胶体凝胶。我们的结果表明,RNP-RNA组件的相行为,超分子组织和材料状态受不同长度尺度上分子相互作用之间的动态相互作用控制。

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