Nanomaterials
with inherent enzyme-mimetic properties
have been
extensively studied in biosensing field, but it is still challenging
to overcome their natively weak enzyme-mimetic activity and further
promote their stabilities. In this work, a three-in-one artificial
enzyme with synergistically enhanced peroxidase-like activity and
outstanding stability is constructed by restricting Au-loaded CeO2 nanorods (NR) (1% Au:CeO2 mass ratio) inside Cu-based
metal–organic frameworks (Cu(PABA)), termed Au1/CeO2 NR@Cu(PABA). It has been demonstrated that the artificial
enzyme possesses significantly improved performance in catalytic decomposition
of H2O2, with ∼2.41 and ∼1.49
times higher activity than its individual constituents (Au1/CeO2 NR and Cu(PABA)), benefiting from the synergistic
effect and the unique restricted structure; owns strong affinities
to substrates, with separately ∼8.21- and ∼3.13-fold
lower Michaelis constants toward H2O2 and o-phenylenediamine, respectively, than horseradish peroxidase;
and exhibits desirable pH (4–12), thermal (30–80 °C),
organic solvent (N,N-dimethylformamide,
acetone, methanol, etc.), and long-term storage (30 days) stabilities,
advantaging practical applications. Taking aforementioned superior
properties of Au1/CeO2 NR@Cu(PABA), a universal
colorimetric/fluorometric dual-mode sensing platform is built and
utilized for detection of biomarkers (e.g., glucose, galactose, and
cholesterol) in biological fluids with satisfactory recoveries (90.2–108%).
This work offers new horizons in designing high-efficiency, stable,
and credible biomimetic catalysts to accelerate future advanced engineering
of nanozymes.