Weththasinghage D. Amith, Vincent T. Chen and Bercem Dutagaci*,
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引用次数: 0
摘要
众所周知,RNA 聚合酶 II(Pol II)的 C 端结构域(CTD)在转录调控中起着至关重要的作用。CTD 的相分离作用也得到了高度认可,这与其调控功能进一步相关。然而,CTD 形成的分子相互作用诱导聚类以驱动相分离,以及 CTD 的磷酸化如何影响聚类,目前还不完全清楚。在这项工作中,我们利用全原子分子动力学模拟研究了两个七肽重复(2CTD)模型在不同磷酸化模式以及蛋白质和离子浓度下的浓缩溶液,以研究聚类行为和驱动聚类形成的分子相互作用。我们的结果表明,盐浓度和磷酸化模式在决定聚类模式方面起着重要作用,特别是在蛋白质浓度较低的情况下。肽间和肽内相互作用以及反离子配位之间的平衡共同影响着磷酸化时的聚类行为。
Clustering of RNA Polymerase II C-Terminal Domain Models upon Phosphorylation
RNA polymerase II (Pol II) C-terminal domain (CTD) is known to have crucial roles in regulating transcription. CTD has also been highly recognized for undergoing phase separation, which is further associated with its regulatory functions. However, the molecular interactions that the CTD forms to induce clustering to drive phase separations and how the phosphorylation of the CTD affects clustering are not entirely known. In this work, we studied the concentrated solutions of two heptapeptide repeat (2CTD) models at different phosphorylation patterns and protein and ion concentrations using all-atom molecular dynamics simulations to investigate clustering behavior and molecular interactions driving the cluster formation. Our results show that salt concentration and phosphorylation patterns play an important role in determining the clustering pattern, specifically at low protein concentrations. The balance between inter- and intrapeptide interactions and counterion coordination together impact the clustering behavior upon phosphorylation.
期刊介绍:
An essential criterion for acceptance of research articles in the journal is that they provide new physical insight. Please refer to the New Physical Insights virtual issue on what constitutes new physical insight. Manuscripts that are essentially reporting data or applications of data are, in general, not suitable for publication in JPC B.