超氧化物
超氧化物歧化酶
氧化应激
化学
铜
肽
SOD1
催化作用
氧气
氧化磷酸化
淀粉样蛋白(真菌学)
生物化学
无机化学
酶
有机化学
作者
Karine Reybier,Sara Ayala,Bruno Aliès,João V. Rodrigues,Susana Bustos Rodriguez,Giovanni La Penna,Fabrice Collin,Cláudio M. Gomes,Christelle Hureau,Peter Faller
标识
DOI:10.1002/anie.201508597
摘要
Abstract Oxidative stress is considered as an important factor and an early event in the etiology of Alzheimer's disease (AD). Cu bound to the peptide amyloid‐β (Aβ) is found in AD brains, and Cu‐Aβ could contribute to this oxidative stress, as it is able to produce in vitro H 2 O 2 and HO . in the presence of oxygen and biological reducing agents such as ascorbate. The mechanism of Cu‐Aβ‐catalyzed H 2 O 2 production is however not known, although it was proposed that H 2 O 2 is directly formed from O 2 via a 2‐electron process. Here, we implement an electrochemical setup and use the specificity of superoxide dismutase‐1 (SOD1) to show, for the first time, that H 2 O 2 production by Cu‐Aβ in the presence of ascorbate occurs mainly via a free O 2 .− intermediate. This finding radically changes the view on the catalytic mechanism of H 2 O 2 production by Cu‐Aβ, and opens the possibility that Cu‐Aβ‐catalyzed O 2 .− contributes to oxidative stress in AD, and hence may be of interest.
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