淀粉样纤维
分子动力学
淀粉样蛋白(真菌学)
蛋白质折叠
化学
蛋白质聚集
生物物理学
纳米技术
淀粉样β
材料科学
计算化学
生物
生物化学
医学
无机化学
病理
疾病
标识
DOI:10.1016/j.sbi.2020.10.019
摘要
In amyloid aggregation diseases soluble proteins coalesce into a wide array of undesirable structures, ranging through oligomers and prefibrillar assemblies to highly ordered amyloid fibrils and plaques. Explicit-solvent all-atom molecular dynamics (MD) simulations of amyloid aggregation have been performed for almost 20 years, revealing valuable information about this phenomenon. However, these simulations are challenged by three main problems. Firstly, current force fields modeling amyloid aggregation are insufficiently accurate. Secondly, the protein concentrations in MD simulations are usually orders of magnitude higher than those used in vitro or found in vivo, which has direct consequences on the aggregates that form. Finally, the third problem is the well-known time-scale limit of MD simulations. In this review I highlight recent approaches to overcome these three limitations.
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