催化作用
化学
钴
活性氧
激进的
基质(水族馆)
氧化应激
DNA损伤
组合化学
生物物理学
DNA
内生
氧气
氧化磷酸化
免疫疗法
细胞毒性T细胞
癌症研究
细胞毒性
辐照
纳米技术
作者
Bo Chen,Xuelin Tao,Yue Wang,Xiaoxiao Wang,Yongzhong Wu,Wanyi Chen
摘要
ABSTRACT Single‐atom nanozymes (SAzymes) have emerged as promising platforms for catalytic therapy owing to their atomic precision and tunable electronic structures. Here, we report an asymmetrically coordinated cobalt SAzyme featuring Co‐N 3 C active sites anchored within a hafnium‐based metal–organic framework (Hf‐MOF). The engineered HfCoNC nanozyme exhibits significantly enhanced peroxidase‐like activity and enables efficient X‐ray–activated catalytic immunotherapy. The asymmetric Co‐N 3 C coordination optimizes substrate adsorption and lowers the reaction energy barrier, thereby accelerating the catalytic reaction. In the tumor microenvironment, HfCoNC efficiently converts endogenous H 2 O 2 into highly cytotoxic hydroxyl radicals (•OH), while low‐dose X‐ray irradiation further amplifies reactive oxygen species (ROS) production. The resulting oxidative stress induces extensive DNA damage and activates the cGAS‐STING signaling pathway. Moreover, the release of Co 2+ ions, together with the co‐delivered STING agonist, further potentiates systemic antitumor immunity, effectively suppressing tumor growth and metastasis. This work provides a promising strategy for developing SAzyme‐based platforms for synergistic catalytic radioimmunotherapy.
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