过氧化氢酶
活性氧
化学
过氧化物酶
光化学
生物化学
酶
作者
Wei Yang,Tianchi Leng,Weicheng Miao,Cao Xiao,H. Chen,Feifei Xu,Yimin Fang
标识
DOI:10.1002/anie.202403581
摘要
Abstract Nanozymes possess multi‐enzyme activities over the natural enzymes, which produce multi‐pathway synergistic effects for varies of biomedical applications. Unfortunately, their multi‐enzyme activities are in fighting, significantly reducing the synergistic effects. Dynamic regulation of their multi‐enzyme activities is the bottleneck for intelligent therapies. Herein, we construct a novel oxygen‐nitrogen functionalized carbon quantum dots (O/N‐CQDs) with peroxidase‐like (Reactive oxygen species (ROS) producer) activity. Interestingly, the peroxidase‐like activity can be reversibly converted to catalase‐like (ROS scavenger) activity under visible light irradiation. It is found that both the peroxidase/catalase‐like activity of O/N‐CQDs can be precisely manipulated by the light intensity. The mechanism of switchable enzyme activities is attributed to the polarization of quinoid nitrogen in polyaniline (PANI) precursor retained on O/N‐CQDs under visible light, which consumes the ROS to produce O 2 and H 2 O. As a proof‐of‐concept demonstration, we are able to non‐intrusively up and down regulate the ROS level in cells successfully by simply switching off and on the light respectively, potentially facilitating the precise medicine based on the development of the disease. Indeed, the photo‐switchable peroxidase/catalase‐like activity of O/N‐CQDs opens a non‐invasive strategy for better manipulations of the multi‐activity of nanozymes, promising their wider and more intelligent biomedical applications.
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