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Protein Interaction with Charged Macromolecules: From Model Polymers to Unfolded Proteins and Post-Translational Modifications

机译:蛋白质与带电大分子的相互作用:从模型聚合物到未折叠的蛋白质和翻译后修饰

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摘要

Interaction of proteins with charged macromolecules is involved in many processes in cells. Firstly, there are many naturally occurred charged polymers such as DNA and RNA, polyphosphates, sulfated glycosaminoglycans, etc., as well as pronouncedly charged proteins such as histones or actin. Electrostatic interactions are also important for “generic” proteins, which are not generally considered as polyanions or polycations. Finally, protein behavior can be altered due to post-translational modifications such as phosphorylation, sulfation, and glycation, which change a local charge of the protein region. Herein we review molecular modeling for the investigation of such interactions, from model polyanions and polycations to unfolded proteins. We will show that electrostatic interactions are ubiquitous, and molecular dynamics simulations provide an outstanding opportunity to look inside binding and reveal the contribution of electrostatic interactions. Since a molecular dynamics simulation is only a model, we will comprehensively consider its relationship with the experimental data.
机译:蛋白质与带电大分子的相互作用涉及细胞的许多过程。首先,存在许多天然存在的带电聚合物,例如DNA和RNA,聚磷酸盐,硫酸化的糖胺聚糖等,以及显着带电的蛋白质,例如组蛋白或肌动蛋白。静电相互作用对于“一般”蛋白质也很重要,“一般”蛋白质通常不被认为是聚阴离子或聚阳离子。最后,由于翻译后修饰(例如磷酸化,硫酸化和糖基化)会改变蛋白质区域的局部电荷,因此可以改变蛋白质的行为。在这里,我们审查分子模型,以研究这种相互作用,从模型聚阴离子和聚阳离子到展开的蛋白质。我们将证明静电相互作用无处不在,并且分子动力学模拟提供了一个绝佳的机会来查看内部结合并揭示静电相互作用的作用。由于分子动力学模拟只是一个模型,因此我们将全面考虑其与实验数据的关系。

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