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金纳米颗粒作为淀粉样纤维形成抑制剂。

Gold nanoparticles as amyloid-like fibrillogenesis inhibitors.

机构信息

Department of Chemistry and Center for Nanoscience and Nanotechnology, National Sun Yat-sen University, Kaohsiung 80424, Taiwan, ROC.

出版信息

Colloids Surf B Biointerfaces. 2013 Dec 1;112:525-9. doi: 10.1016/j.colsurfb.2013.08.029. Epub 2013 Aug 28.

Abstract

Amyloid aggregates are one of the likely key factors leading to the development of Alzheimer's disease (AD) and other amyloidosis associated diseases. Several recent studies have shown that some anti-diabetic drugs have a positive therapeutic effect on AD patients by crossing the blood brain barrier (BBB) and preventing or reducing insulin resistance. Nanoparticles (NPs) or nanoscale objects (<600Da.), are able to cross the BBB at low concentrations, and can specifically target amyloidogenic structures. Thus, NPs are fast becoming indispensable tools for directed drug delivery, particularly when targeting structures or regions in the brain. Here, we have explored the inhibitory effect of gold nanoparticles (AuNPs) on the fibrillogenesis process of insulin fibrils. We found that when AuNPs were co-incubated with insulin, the structural transformation into amyloid-like fibrils was delayed by about a week. Further, the fibrils that formed, exhibited altered structure, shape, and dynamics, which further reduced fibril growth, and the stability of available amyloid-like fibrils with cross-β structure for aggregation. Our results demonstrate that AuNPs disrupt insulin amyloid fibrillation resulting in fibrils that are shorter and more compact, and thus may serve a useful role in new therapeutic and diagnostic strategies for amyloid-related disorders.

摘要

淀粉样蛋白聚集物是导致阿尔茨海默病(AD)和其他与淀粉样变性相关疾病发展的关键因素之一。最近的几项研究表明,一些抗糖尿病药物通过穿透血脑屏障(BBB)并预防或减少胰岛素抵抗,对 AD 患者具有积极的治疗作用。纳米颗粒(NPs)或纳米级物体(<600Da.)能够以低浓度穿透 BBB,并能够特异性靶向淀粉样结构。因此,NPs 正在迅速成为靶向药物递送的不可或缺的工具,特别是在针对大脑中的结构或区域时。在这里,我们研究了金纳米颗粒(AuNPs)对胰岛素纤维形成过程的抑制作用。我们发现,当 AuNPs 与胰岛素共孵育时,结构向类似淀粉样纤维的转变被延迟了大约一周。此外,形成的纤维表现出改变的结构、形状和动力学,这进一步降低了纤维的生长速度,并降低了具有交叉-β结构的可用类似淀粉样纤维的稳定性,从而有利于聚集。我们的结果表明,AuNPs 破坏了胰岛素淀粉样纤维的形成,导致纤维更短、更紧凑,因此可能在淀粉样相关疾病的新治疗和诊断策略中发挥有用作用。

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