钒
生物催化
活性氧
材料科学
酶
组合化学
生化工程
纳米技术
可再生能源
电子转移
人工酶
电子传输链
化学
活动站点
代谢工程
氧气
氧化还原
定向进化
蛋白质工程
作者
Zihe Wu,Ling Li,Ting Wang,Sutong Xiao,Xiaoming Xu,Xiaohua Luo,Xiaolin Wang,Shuang Li,Yi Wang,Li Qiu,Chong Cheng
摘要
ABSTRACT Biocatalytic generation of reactive oxygen species (ROS) by artificial enzymes offers a promising strategy for treating diverse diseases, including pathogenic infections and malignancies. However, the sluggish ROS biocatalytic efficiency and unstable active sites have hindered their potential clinical translation. Here, inspired by natural vanadium haloperoxidases and NADPH oxidase‐based ROS‐catalytic systems, we report the de novo design of a sono‐activated artificial vanadium enzyme (V x+ ‐SonoAE) for efficient and renewable ROS nanobiocatalytic therapies. By mimicking the electron transport chains and active VO 4 centers in natural enzymes, our innovative bionic approach not only yields efficient, robust, and precise vanadium active sites on TiO 2 but also enables continuous regeneration of redox centers during ROS biocatalysis via efficient electron transfer from sono‐activated TiO 2 to the V x+ site. Consequently, the V x+ ‐SonoAE achieves remarkable ROS‐catalytic performance with a superior turnover number (TON = 54 × 10 −3 s −1 ) that far surpasses the reported state‐of‐the‐art metal oxides‐based nanobiocatalysts. Moreover, this new artificial enzyme system demonstrates exceptional therapeutic efficiency in infection control and tumor regression with sustained and sono‐activated treatment properties. This work establishes a new paradigm for designing efficient and renewable nanobiocatalysts, combining fundamental insights from natural enzymatic systems with advanced materials engineering to create robust therapeutic platforms with long‐term efficacy.
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