Juan Wang, Yujia Ren, Baojian Huang, Chuanping Li, Shuai Qin, Shaojun Dong, Daoqing Fan
Exploring novel-type nanozymes with programmatically manipulated enzyme-mimicking activity for targets’ accurate identification and multimodal biosensing represents one of the most fascinating yet challenging research frontiers. Herein, taking DNAs as programmable biotemplates, we prepared bimetallic PtAg nanocluster-zyme via simple in situ reduction. Among them, the A20-templated PtAg nanozyme exhibited superior peroxidase-like (POD-like) activity, as confirmed by optical analyses, steady-state kinetics, and electron paramagnetic resonance spectroscopy, with •O 2 – and •OH identified as the primary reactive oxygen species. Taking Pt-AMP with the Pt–N 4 coordination structure as representative, pluralistic DFT calculations were performed. Corresponding results manifested the superior affinity of nanozyme for H 2 O 2 and TMB, the elongated O–O bond length of H 2 O 2 and facilitated electron-transfer ability at the catalytic core. Subsequently, by harnessing the efficient catalytic oxidation of TMB and AR, we fabricated a colorimetric-photothermal-fluorescent trimodal sensing platform for assessing total antioxidant capacity and alkaline phosphatase activity. Superior to previous single/dual-modal biosensors, this work demonstrated significant advantages in sensitivity, reliability, and accuracy, and showed acceptable adaptability in diversified real matrices (human serum, tablets, and beverages). Furthermore, we fabricated target-responsive cascade logic circuits by virtue of the proper incorporation of trimodal signals and Boolean logic, and achieved the smart recognition of targets. This work not only provided a mild, simple, and efficient biotemplated approach for the programmable tuning of noble-metal nanozymes’ catalytic activity but also enlightened novel pathways for the operation of logic-empowered intelligent biosensors.