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

IF 16 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
ACS Nano Pub Date : 2025-03-05 DOI:10.1021/acsnano.4c16272
Xinghua Chen, Yi Wu, Yunlong Qin, Raanan Carmieli, Inna Popov, Vitaly Gutkin, Chunhai Fan, Itamar Willner
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Abstract

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.

Abstract Image

分子印迹聚苯胺包被的铜沸石咪唑酸框架纳米颗粒:模拟尿酸酶的“多纳米酶”催化尿酸氧化
纳米酶催化功能的缺点之一在于其催化活性适中,这是由于缺乏将反应底物集中在纳米酶催化界面上的有效结合位点。在催化界面集中底物的方法是提高纳米酶功能的关键。本研究通过设计尿酸(UA)分子印迹聚苯胺(PAn)包覆cu -沸石咪唑酸框架(Cu-ZIF)纳米颗粒作为卓越的纳米酶,“多纳米酶”,催化H2O2氧化UA生成尿囊素(过氧化物酶活性)或有氧,模拟尿酸酶,将UA氧化生成尿囊素(氧化酶活性)。裸Cu-ZIF纳米颗粒仅显示过氧化物酶活性,而非印迹pan包覆的Cu-ZIF纳米颗粒显示出抑制过氧化物酶活性,而分子印迹pan包覆的Cu-ZIF纳米颗粒显示出6.1倍的过氧化物酶活性增强,这归功于催化纳米颗粒界面处UA底物的浓度。此外,印迹pan包覆的Cu-ZIF纳米颗粒在裸颗粒中缺乏催化UA有氧氧化成尿囊素的功能,这表明分子印迹的多纳米酶具有进化的催化功能。该体系的机理表征表明,在PAn涂层的UA分子印迹过程中,Cu+反应单元在Cu- zif纳米颗粒中生成,这些反应单元为生成O2 -•提供了反应位点,作为引导纳米颗粒氧化酶活性的中间剂。该研究强调了分子印迹多纳米酶在裸纳米酶缺乏的催化途径中的实际应用,从而扩大了纳米酶系统的范围。
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来源期刊
ACS Nano
ACS Nano 工程技术-材料科学:综合
CiteScore
26.00
自引率
4.10%
发文量
1627
审稿时长
1.7 months
期刊介绍: ACS Nano, published monthly, serves as an international forum for comprehensive articles on nanoscience and nanotechnology research at the intersections of chemistry, biology, materials science, physics, and engineering. The journal fosters communication among scientists in these communities, facilitating collaboration, new research opportunities, and advancements through discoveries. ACS Nano covers synthesis, assembly, characterization, theory, and simulation of nanostructures, nanobiotechnology, nanofabrication, methods and tools for nanoscience and nanotechnology, and self- and directed-assembly. Alongside original research articles, it offers thorough reviews, perspectives on cutting-edge research, and discussions envisioning the future of nanoscience and nanotechnology.
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