NAD(P)H氧化酶
烟酰胺腺嘌呤二核苷酸
再生(生物学)
氧化酶试验
生物化学
NAD+激酶
烟酰胺腺嘌呤二核苷酸磷酸
化学
氧化还原酶
超氧化物歧化酶
活性氧
过氧化物酶
生物
细胞生物学
酶
作者
Xiaoyu Liu,Zhen Wan,Ke Chen,Yuxing Yan,Xuyan Li,Yili Wang,Miaoyu Wang,Ruoli Zhao,Jiahui Pei,Lijie Zhang,Si Sun,Jiarong Li,Xinzhu Chen,Xin Qi,Shaofang Zhang,Shuangjie Liu,Hao Wang,Changlong Liu,Xiaoyu Mu,Xiaodong Zhang
出处
期刊:Nano Letters
[American Chemical Society]
日期:2024-04-15
被引量:1
标识
DOI:10.1021/acs.nanolett.4c00546
摘要
Excessive accumulation of reduced nicotinamide adenine dinucleotide (NADH) within biological organisms is closely associated with many diseases. It remains a challenge to efficiently convert superfluous and detrimental NADH to NAD+. NADH oxidase (NOX) is a crucial oxidoreductase that catalyzes the oxidation of NADH to NAD+. Herein, M1M2 (Mi=V/Mn/Fe/Co/Cu/Mo/Rh/Ru/Pd, i = 1 or 2) mated-atom nanozymes (MANs) are designed by mimicking natural enzymes with polymetallic active centers. Excitingly, RhCo MAN possesses excellent and sustainable NOX-like activity, with Km-NADH (16.11 μM) being lower than that of NOX-mimics reported so far. Thus, RhCo MAN can significantly promote the regeneration of NAD+ and regulate macrophage polarization toward the M2 phenotype through down-regulation of TLR4 expression, which may help to recover skin regeneration. However, RhRu MAN with peroxidase-like activity and RhMn MAN with superoxide dismutase-like activity exhibit little modulating effects on eczema. This work provides a new strategy to inhibit skin inflammation and promote skin regeneration.
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