碱性磷酸酶
免疫分析
化学
荧光
酶
尿
融合蛋白
色谱法
生物化学
抗体
生物
重组DNA
免疫学
量子力学
基因
物理
作者
Jingqian Huo,Zhenfeng Li,Debin Wan,Dongyang Li,Meng Qi,Bogdan B. Barnych,Natalia Vasylieva,Jinlin Zhang,Bruce D. Hammock
标识
DOI:10.1021/acs.jafc.8b04521
摘要
3-Phenoxybenzoic acid (3-PBA) is a human urinary metabolite of many pyrethroid insecticides and can be used as a biomarker to monitor human exposure to these pesticides. A rapid and sensitive direct competitive fluorescence enzyme immunoassay (dc-FEIA) for detecting 3-PBA on the basis of a nanobody (Nb)–alkaline phosphatase (AP) fusion protein was developed. The anti-3-PBA Nb–AP fusion protein was expressed and purified. The 50% inhibitory concentration (IC 50 ) and linear range of dc-FEIA were 0.082 and 0.015–0.447 ng/mL, respectively, with a detection limit of 0.011 ng/mL. The IC 50 of dc-FEIA was improved by nearly ten times compared with those of one-step and three-step direct competitive enzyme-linked immunosorbent assay (dc-ELISA). Spiked urine samples were detected by both dc-FEIA and liquid chromatography–mass spectrometry (LC-MS), and the results showed good consistency between the two analysis methods, indicating the reliability of dc-FEIA based on the Nb–AP fusion protein for detecting 3-PBA in urine.
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