淀粉样蛋白(真菌学)
纳米医学
机制(生物学)
淀粉样变性
手性(物理)
淀粉样纤维
纳米技术
神经科学
化学
疾病
淀粉样β
计算生物学
医学
生物
材料科学
纳米颗粒
内科学
哲学
物理
认识论
无机化学
量子力学
手征对称破缺
Nambu–Jona Lasinio模型
夸克
作者
Zhe Zhou,Youquan Gu,Hang‐Xing Wang
标识
DOI:10.1021/acschemneuro.1c00544
摘要
Alzheimer's disease (AD) is a progressive neurodegenerative disorder characterized by an imbalance between the production and clearance of amyloid-β (Aβ) species. AD not only influences the life quality of the patients but also heavily burdens the families and society. Therefore, it is an urgent mission to research and develop some new anti-amyloid aggregation drugs. In recent years, there were research and development of engineered nanostructures as Aβ amyloid inhibitors have attracted extensive attention and become a new frontier in nanomedicine. The effects of nanostructural surface properties (e.g., morphology, charge, hydrophobicity) on inhibition of Aβ aggregation are modulated by adsorbed Aβ peptides. Nevertheless, chirality has been seldom considered in recognition of Aβ species and modulation of Aβ aggregations. Moreover, a more relevant question for chiral inhibitors is little known about the molecular mechanism of how to interface chiral effects Aβ targeting recognition and effective mitigation of amyloidosis at the molecular level. Herein, we review recent experimental and theoretical results acquired in the specific areas of artificial chiral nanostructure inhibitors. This article will be essential to provide a microlevel insight into the effects of chiral nanointerfaces on amyloidosis processes as well as the development of chiral inhibitor drugs against Aβ fibrillation.
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