Viles John H
Department of Biochemistry, SBBS, Queen Mary University of London UK.
Angew Chem Weinheim Bergstr Ger. 2023 Jun 19;135(25):e202215785. doi: 10.1002/ange.202215785. Epub 2023 Mar 30.
The accumulation of the amyloid-β peptides (Aβ) is central to the development of Alzheimer's disease. The mechanism by which Aβ triggers a cascade of events that leads to dementia is a topic of intense investigation. Aβ self-associates into a series of complex assemblies with different structural and biophysical properties. It is the interaction of these oligomeric, protofibril and fibrillar assemblies with lipid membranes, or with membrane receptors, that results in membrane permeability and loss of cellular homeostasis, a key event in Alzheimer's disease pathology. Aβ can have an array of impacts on lipid membranes, reports have included: a carpeting effect; a detergent effect; and Aβ ion-channel pore formation. Recent advances imaging these interactions are providing a clearer picture of Aβ induced membrane disruption. Understanding the relationship between different Aβ structures and membrane permeability will inform therapeutics targeting Aβ cytotoxicity.
淀粉样β肽(Aβ)的积累是阿尔茨海默病发展的核心。Aβ引发一系列导致痴呆的事件的机制是一个深入研究的课题。Aβ自组装成一系列具有不同结构和生物物理特性的复杂聚集体。正是这些寡聚体、原纤维和纤维状聚集体与脂质膜或膜受体的相互作用,导致了膜通透性和细胞内稳态的丧失,这是阿尔茨海默病病理学中的一个关键事件。Aβ可对脂质膜产生一系列影响,报告包括:铺展效应;去污剂效应;以及Aβ离子通道孔的形成。对这些相互作用进行成像的最新进展正在更清楚地呈现Aβ诱导的膜破坏情况。了解不同Aβ结构与膜通透性之间的关系将为针对Aβ细胞毒性的治疗提供依据。