Molecularly Imprinted Polyaniline-Coated Cu-Zeolitic Imidazolate Framework Nanoparticles: Uricase-Mimicking “Polynanozyme” Catalyzing Uric Acid Oxidation

催化作用 尿囊素 化学 纳米颗粒 咪唑酯 聚苯胺 分子印迹 催化氧化 过氧化物酶 组合化学 纳米技术 无机化学 材料科学 有机化学 聚合物 选择性 聚合
作者
Xinghua Chen,Yi Wu,Yunlong Qin,Raanan Carmieli,Inna Popov,Vitaly Gutkin,Chunhai Fan,Itamar Willner
出处
期刊:ACS Nano [American Chemical Society]
标识
DOI:10.1021/acsnano.4c16272
摘要

One of the drawbacks of nanozyme catalytic functions rests in their moderate catalytic activities due to the lack of effective binding sites concentrating the reaction substrate at the nanozyme catalytic interface. Methods to concentrate the substrates at the catalytic interface are essential to improving nanozyme functions. The present study addresses this goal by designing uric acid (UA) molecular-imprinted polyaniline (PAn)-coated Cu-zeolitic imidazolate framework (Cu-ZIF) nanoparticles as superior nanozymes, "polynanozymes", catalyzing the H2O2 oxidation of UA to allantoin (peroxidase activity) or the aerobic, uricase mimicking, oxidation of UA to allantoin (oxidase activity). While bare Cu-ZIF nanoparticles reveal only peroxidase activity and the nonimprinted PAn-coated Cu-ZIF nanoparticles reveal inhibited peroxidase activity, the molecular-imprinted PAn-coated Cu-ZIF nanoparticles reveal a 6.1-fold enhanced peroxidase activity, attributed to the concentration of the UA substrate at the catalytic nanoparticle interface. Moreover, the catalytic aerobic oxidation of UA to allantoin by the imprinted PAn-coated Cu-ZIF nanoparticles is lacking in the bare particles, demonstrating the evolved catalytic functions in the molecularly imprinted polynanozymes. Mechanistic characterization of the system reveals that within the UA molecular imprinting process of the PAn coating, Cu+ reactive units are generated within the Cu-ZIF nanoparticles, and these provide reactive sites for generating O2-• as an intermediate agent guiding the oxidase activities of the nanoparticles. The study highlights the practical utility of molecular-imprinted polynanozymes in catalytic pathways lacking in the bare nanozymes, thus broadening the scope of nanozyme systems.
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