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基于脲酶包封金属有机骨架的免疫测定法,用于通过 pH 计作为读出器进行灵敏检测食源性病原体。

Immunoassay based on urease-encapsulated metal-organic framework for sensitive detection of foodborne pathogen with pH meter as a readout.

机构信息

Key Laboratory of Hunan Province for Study and Utilization of Ethnic Medicinal Plant Resources, College of Biological and Food Engineering, Huaihua University, Huaihua, 418000, People's Republic of China.

College of Chemistry and Chemical Engineering, Jiangxi Normal University, Nanchang, 330022, People's Republic of China.

出版信息

Mikrochim Acta. 2022 Sep;189(9):358. doi: 10.1007/s00604-022-05462-8. Epub 2022 Aug 30.

Abstract

The potential of enzyme-encapsulated metal-organic framework (MOF) as an antibody label for the construction of enzyme-linked immunosorbent assay (ELISA) is demonstrated. Zeolitic imidazolate framework-90 (ZIF-90) was employed as a MOF model to load urease and pig immunoglobulin G (IgG) antibody. This leads to the production of U@ZIF-90/IgG composite, in which urease was encapsulated in ZIF-90 to form U@ZIF-90 for amplifying the detection signal, while IgG was anchored on the surface of U@ZIF-90 for specifically recognizing Staphylococcus aureus (S. aureus). Benefiting from the unique porous structure of ZIF-90, the U@ZIF-90 not only allows urease to be encapsulated with an ultrahigh loading efficiency, but also shields the loaded urease against harsh environments. The U@ZIF-90 shows a threefold higher catalytic activity than free urease due to the confinement effect. These findings lead to an ELISA with greatly enhanced sensitivity for S. aureus detection. By using a portable pH meter as a readout, the ELISA has a linear response that covers 10 to 10 CFU/mL S. aureus with a detection limit of 1.96 CFU/mL and exhibits high selectivity over other bacteria. The successful determination of S. aureus in milk samples demonstrates the applicability of the ELISA in a complex biological matrix.

摘要

酶封装金属有机骨架(MOF)作为抗体标记物用于构建酶联免疫吸附测定(ELISA)的潜力得到了证明。沸石咪唑酯骨架-90(ZIF-90)被用作 MOF 模型来负载脲酶和猪免疫球蛋白 G(IgG)抗体。这导致了 U@ZIF-90/IgG 复合物的产生,其中脲酶被封装在 ZIF-90 中以形成 U@ZIF-90 用于放大检测信号,而 IgG 则锚定在 U@ZIF-90 的表面上用于特异性识别金黄色葡萄球菌(S. aureus)。得益于 ZIF-90 的独特多孔结构,U@ZIF-90 不仅允许脲酶以超高负载效率被封装,而且还保护负载的脲酶免受恶劣环境的影响。由于限域效应,U@ZIF-90 的催化活性比游离脲酶高三倍。这些发现导致了用于 S. aureus 检测的 ELISA 灵敏度大大提高。通过使用便携式 pH 计作为读出设备,ELISA 具有线性响应,涵盖 10 至 10^CFU/mL S. aureus,检测限为 1.96 CFU/mL,并对其他细菌表现出高选择性。在牛奶样本中成功测定 S. aureus 证明了 ELISA 在复杂生物基质中的适用性。

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