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Bubble-templated synthesis of nanocatalyst Co/C as NADH oxidase mimic

Designing highly active nanozymes for various enzymatic reactions remains a challenge in practical applications and fundamental research. In this work, by studying the catalytic functions of natural NADH oxidase (NOX), we devised and synthesized a porous carbon-supported cobalt catalyst (Co/C) to mi...

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Detalles Bibliográficos
Autores principales: Chen, Jinxing, Zheng, Xiliang, Zhang, Jiaxin, Ma, Qian, Zhao, Zhiwei, Huang, Liang, Wu, Weiwei, Wang, Ying, Wang, Jin, Dong, Shaojun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8897313/
https://www.ncbi.nlm.nih.gov/pubmed/35261777
http://dx.doi.org/10.1093/nsr/nwab186
Descripción
Sumario:Designing highly active nanozymes for various enzymatic reactions remains a challenge in practical applications and fundamental research. In this work, by studying the catalytic functions of natural NADH oxidase (NOX), we devised and synthesized a porous carbon-supported cobalt catalyst (Co/C) to mimic NOX. The Co/C can catalyze dehydrogenation of NADH and transfers electrons to O(2) to produce H(2)O(2). Density functional theory calculations reveal that the Co/C can catalyze O(2) reduction to H(2)O(2) or H(2)O considerably. The Co/C can also mediate electron transfer from NADH to heme protein cytochrome c, thereby exhibiting cytochrome c reductase-like activity. The Co/C nanoparticles can deplete NADH in cancer cells, induce increase of the reactive oxygen species, lead to impairment of oxidative phosphorylation and decrease in mitochondrial membrane potential, and cause ATP production to be damaged. This ‘domino effect’ facilitates the cell to approach apoptosis.