Strodel Birgit
Institute of Biological Information Processing, Structural Biochemistry (IBI-7), Forschungszentrum Jülich, Jülich, Germany.
Institute of Theoretical and Computational Chemistry, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Bioessays. 2025 Sep;47(9):e70039. doi: 10.1002/bies.70039. Epub 2025 Jul 11.
The amyloid-β peptide (Aβ), implicated in Alzheimer's disease, exhibits significant polymorphism. At the monomer level, Aβ can adopt disordered, helical, and β-hairpin structures, influenced by environmental conditions. Both oligomeric and fibrillar states, characterized by the prevalence of β-sheets, are polymorphic in the arrangement of β-strands. This chameleon-like behavior arises from Aβ's unique sequence and relatively flat energy landscape, which facilitates aggregation and may contribute to the prevalence of Alzheimer's disease, while also enabling disaggregation, thus slowing disease progression. In contrast, Creutzfeldt-Jakob disease, which is much rarer, progresses far more rapidly, likely due to the steeper energy landscape of the prion protein.
与阿尔茨海默病相关的β淀粉样肽(Aβ)表现出显著的多态性。在单体水平上,Aβ可呈现无序、螺旋和β发夹结构,受环境条件影响。以β折叠为主的寡聚态和纤维状态在β链排列上均具有多态性。这种类似变色龙的行为源于Aβ独特的序列和相对平缓的能量态势,这既有利于聚集,可能导致阿尔茨海默病的高发,同时也能使聚集物解聚,从而减缓疾病进展。相比之下,更为罕见的克雅氏病进展要快得多,这可能是由于朊病毒蛋白的能量态势更为陡峭。