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用于唾液中SARS-CoV-2刺突蛋白定量比率电化学检测的分子印迹病毒蛋白集成锌-铜-铟-硒-磷量子点超晶格

Molecularly Imprinted Viral Protein Integrated Zn-Cu-In-Se-P Quantum Dots Superlattice for Quantitative Ratiometric Electrochemical Detection of SARS-CoV-2 Spike Protein in Saliva.

作者信息

Adeniyi Kayode Omotayo, Oyinlola Kayode, Achadu Ojodomo J, Menard Herve, Grillo Federico, Yang Zhugen, Adegoke Oluwasesan

机构信息

Leverhulme Research Centre for Forensic Science, School of Science & Engineering, University of Dundee, Dundee DD1 4GH, U.K.

School of Health and Life Sciences, and National Horizon Centre, Teesside University, Middlesbrough TS1 3BA, U.K.

出版信息

ACS Appl Nano Mater. 2024 Jul 24;7(15):17630-17647. doi: 10.1021/acsanm.4c02882. eCollection 2024 Aug 9.

Abstract

Solution-processable colloidal quantum dots (QDs) are promising materials for the development of rapid and low-cost, next-generation quantum-sensing diagnostic systems. In this study, we report on the synthesis of multinary Zn-Cu-In-Se-P (ZCISeP) QDs and the application of the QDs-modified electrode (QDs/SPCE) as a solid superlattice transducer interface for the ratiometric electrochemical detection of the SARS-CoV-2-S1 protein in saliva. The ZCISeP QDs were synthesized through the formation of In(Zn)PSe QDs from InP QDs, followed by the incorporation of Cu cations into the crystal lattice via cation exchange processes. A viral-protein-imprinted polymer film was deposited onto the QDs/SPCE for the specific binding of SARS-CoV-2. Molecular imprinting of the virus protein was achieved using a surface imprinting electropolymerization strategy to create the MIP@QDs/SPCE nanosensor. Characterization through spectroscopic, microscopic, and electrochemical techniques confirmed the structural properties and electronic-band state of the ZCISeP QDs. Cyclic voltammetry studies of the QDs/SPCE superlattice confirmed efficient electron transport properties and revealed an intraband gap energy state with redox peaks attributed to the Cu defects. Binding of SARS-CoV-2-S1 to the MIP@QDs/SPCE cavities induced a gating effect that modulated the Fe(CN) and Cu redox processes at the nanosensor interface, producing dual off/on ratiometric electrical current signals. Under optimal assay conditions, the nanosensor exhibited a wide linear detection range (0.001-100 pg/mL) and a low detection limit (0.34 pg/mL, 4.6 fM) for quantitative detection of SARS-CoV-2-S1 in saliva. The MIP@QDs/SPCE nanosensor demonstrated excellent selectivity against nonspecific protein targets, and the integration with a smartphone-based potentiostat confirmed the potential for point-of-care applications.

摘要

可溶液处理的胶体量子点(QDs)是用于开发快速且低成本的下一代量子传感诊断系统的有前途的材料。在本研究中,我们报告了多元Zn-Cu-In-Se-P(ZCISeP)量子点的合成以及量子点修饰电极(QDs/SPCE)作为固体超晶格换能器界面在唾液中SARS-CoV-2-S1蛋白的比率电化学检测中的应用。通过由InP量子点形成In(Zn)PSe量子点,随后通过阳离子交换过程将Cu阳离子掺入晶格中来合成ZCISeP量子点。将病毒蛋白印迹聚合物膜沉积在QDs/SPCE上以实现SARS-CoV-2的特异性结合。使用表面印迹电聚合策略实现病毒蛋白的分子印迹,以创建MIP@QDs/SPCE纳米传感器。通过光谱、显微镜和电化学技术进行的表征证实了ZCISeP量子点的结构性质和电子能带状态。对QDs/SPCE超晶格的循环伏安研究证实了有效的电子传输性质,并揭示了具有归因于Cu缺陷的氧化还原峰的带内隙能态。SARS-CoV-2-S1与MIP@QDs/SPCE腔的结合诱导了门控效应,该效应调节了纳米传感器界面处的Fe(CN)和Cu氧化还原过程,产生双关/开比率电流信号。在最佳检测条件下,该纳米传感器在唾液中SARS-CoV-2-S1的定量检测中表现出宽线性检测范围(0.001-100 pg/mL)和低检测限(0.34 pg/mL,4.6 fM)。MIP@QDs/SPCE纳米传感器对非特异性蛋白质靶标表现出优异的选择性,并且与基于智能手机的恒电位仪集成证实了其即时检测应用的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8509/11320384/3741135a7cea/an4c02882_0010.jpg

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