Proton-Regulated Catalytic Activity of Nanozymes for Dual-Modal Bioassay of Urease Activity

化学 生物测定 生物传感器 尿素酶 催化作用 光电流 介孔材料 纳米传感器 纳米技术 生物化学 组合化学 物理 生物 遗传学 材料科学 光电子学
作者
Mingwang Liu,Guojuan Chen,Ying Qin,Jinli Li,Liuyong Hu,Wenling Gu,Chengzhou Zhu
出处
期刊:Analytical Chemistry [American Chemical Society]
卷期号:93 (28): 9897-9903 被引量:34
标识
DOI:10.1021/acs.analchem.1c01999
摘要

Benefiting from the merits of high stability and superior activity, nanozymes are recognized as promising alternatives to natural enzymes. Despite the great leaps in the field of therapy and colorimetric sensing, the development of highly sensitive nanozyme-involved photoelectrochemical (PEC) biosensors is still in its infancy. Specifically, the investigation of multifunctional nanozymes facilitating different catalytic reactions remains largely unexplored due to the difficulty in synergistically amplifying the PEC signals. In this work, mesoporous trimetallic AuPtPd nanospheres were synthesized with both efficient oxidase and peroxidase-like activities, which can synergistically catalyze the oxidation of 4-chloro-1-naphthol to produce benzo-4-chlorohexadienone precipitation on the surface of photoactive materials, and thus lead to the decreased photocurrent as well as increased charge-transfer resistance. Inspired by the proton-dependent catalytic activity of nanozymes, a self-regulated dual-modal PEC and electrochemical bioassay of urease activity was innovatively established by in situ regulating the activity of AuPtPd nanozymes through urease-mediated proton-consuming enzymatic reactions, which can remarkably improve the accuracy of the assay. Meanwhile, the determination of urease activity in spiked human saliva samples was successfully realized, indicating the reliability of the biosensor and its application prospects in clinical diagnosis.
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