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Mobile obstacles accelerate and inhibit the bundle formation in two-patch colloidal particle

机译:移动障碍加速并抑制双贴片胶体颗粒中的束形成

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Aggregation of protein into bundles is responsible for many neurodegenerative diseases. In this work, we show how two-patch colloidal particles self-assemble into chains and a sudden transition to bundles takes place by tuning the patch size and solvent condition. We study the kinetics of formation of chains, bundles, and networklike structures using patchy Brownian cluster dynamics. We also analyze the ways to inhibit and accelerate the formation of these bundles. We show that in the presence of inert immobile obstacles, the kinetics of formation of bundles slows down. However, in the presence of mobile aggregating particles, which exhibit interspecies hard sphere repulsion and intraspecies attraction, the kinetics of bundle formation accelerates slightly. We also show that if we introduce mobile obstacles, which exhibit interspecies attraction and intraspecies hard sphere repulsion, the kinetics of formation of bundles is inhibited. This is similar to the inhibitory effect of peptide P4 on the formation of insulin fibers. We are providing a model of mobile obstacles undergoing directional interactions to inhibit the formation of bundles. Published under license by AIP Publishing.
机译:蛋白质聚集成束是对许多神经变性疾病的原因。在这项工作中,我们展示了双贴片胶体颗粒如何通过调整贴片尺寸和溶剂条件来自组装成链子并突然过渡到捆绑。我们使用斑驳的布朗群体动态研究链条,捆绑和网络状结构的形成动力学。我们还分析了抑制和加速这些捆绑形成的方法。我们表明,在存在惰性的不动障碍物中,捆绑的形成动力学减慢了。然而,在存在移动聚集颗粒的情况下,其表现出差距离球体排斥和缠绕物的吸引力,束形成的动力学略微加速。我们还表明,如果我们引入移动障碍,它展示了涉及的景点和绞入物的障碍物排斥,则捆绑捆绑的动力学被抑制。这类似于肽P4对胰岛素纤维形成的抑制作用。我们正在提供经历定向相互作用的移动障碍模型,以抑制捆绑的形成。通过AIP发布在许可证下发布。

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