纤维
原子力显微镜
生物物理学
材料科学
淀粉样蛋白(真菌学)
显微镜
淀粉样纤维
化学
纳米技术
淀粉样β
蛋白质聚集
生物
疾病
生物化学
医学
病理
无机化学
作者
Jozef Adamčík,Jin‐Mi Jung,Jérôme Flakowski,Paolo De Los Rios,Giovanni Dietler,Raffaele Mezzenga
标识
DOI:10.1038/nnano.2010.59
摘要
The aggregation of proteins is central to many aspects of daily life, including food processing, blood coagulation, eye cataract formation disease and prion-related neurodegenerative infections. However, the physical mechanisms responsible for amyloidosis-the irreversible fibril formation of various proteins that is linked to disorders such as Alzheimer's, Creutzfeldt-Jakob and Huntington's diseases-have not yet been fully elucidated. Here, we show that different stages of amyloid aggregation can be examined by performing a statistical polymer physics analysis of single-molecule atomic force microscopy images of heat-denatured beta-lactoglobulin fibrils. The atomic force microscopy analysis, supported by theoretical arguments, reveals that the fibrils have a multistranded helical shape with twisted ribbon-like structures. Our results also indicate a possible general model for amyloid fibril assembly and illustrate the potential of this approach for investigating fibrillar systems.
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