Wang Zhengdi, Wen Hailong, Zheng Ceping, Wang Xiangming, Yin Sijie, Song Ningning, Liang Minmin
Experimental Center of Advanced Materials, School of Materials Science & Engineering, Beijing Institute of Technology, Beijing 100081, China.
Institute of Biophysics, Chinese Academy of Sciences, University of Chinese Academy of Sciences, Beijing 100101, China.
ACS Appl Mater Interfaces. 2025 Jan 8;17(1):583-593. doi: 10.1021/acsami.4c17416. Epub 2024 Dec 17.
Neurodegenerative diseases like Parkinson's disease (PD) are intimately associated with oxidative stress due to the excessive highly reactive oxygen species (ROS), leading to the damage of dopaminergic neurons. Herein, we develop a Co-Cu dual-atom nanozyme (CoCu-DAzyme) by uniformly anchoring Co and Cu active sites onto an AlO(OH) substrate that exhibits remarkable catalase-like catalytic activity, far exceeding that of the Co or Cu single-atom counterparts. The following density functional theory calculations reveal that the Co sites efficiently enable HO adsorption, while Cu sites promote charge transfer, synergistically promoting the catalytic decomposition of HO into HO and O. Encouragingly, the developed CoCu-DAzyme notably ameliorates α-synuclein aggregation and alleviates the motor dysfunction inPD models by substantively scavenging ROS. This research shows a novel therapeutic strategy for oxidative-stress-related neurodegenerative disorders by developing well-engineered nanozymes.
帕金森病(PD)等神经退行性疾病与由于过量高活性氧(ROS)导致的氧化应激密切相关,从而导致多巴胺能神经元受损。在此,我们通过将Co和Cu活性位点均匀锚定在AlO(OH)载体上,开发了一种Co-Cu双原子纳米酶(CoCu-DAzyme),该纳米酶表现出显著的过氧化氢酶样催化活性,远远超过Co或Cu单原子对应物。随后的密度泛函理论计算表明,Co位点有效地促进HO吸附,而Cu位点促进电荷转移,协同促进HO催化分解为HO和O。令人鼓舞的是,所开发的CoCu-DAzyme通过大量清除ROS,显著改善了α-突触核蛋白聚集,并减轻了PD模型中的运动功能障碍。这项研究通过开发精心设计的纳米酶,展示了一种针对氧化应激相关神经退行性疾病的新型治疗策略。