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基于受体的化学发光酶联免疫吸附测定法测定牛奶中的四环素。

A receptor-based chemiluminescence enzyme linked immunosorbent assay for determination of tetracyclines in milk.

机构信息

College of Veterinary Medicine, Hebei Agricultural University, 071000, Baoding Hebei, China.

College of Veterinary Medicine, Hebei Agricultural University, 071000, Baoding Hebei, China.

出版信息

Anal Biochem. 2019 Jan 1;564-565:40-46. doi: 10.1016/j.ab.2018.10.017. Epub 2018 Oct 16.

Abstract

This study for the first time reported a receptor based chemiluminescence immunoassay for analysis of tetracyclines. During the experiments, the gene of TetR protein was transformed into Rosetta-gami(DE3) to express a receptor, and its recognition mechanism for 5 tetracyclines was studied by using molecular docking technique. Results showed that hydrophobic interaction and Pi-Pi bond were the main intermolecular forces responsible for TetR-tetracyclines binding, and the D ring was the main receptor binding position in tetracyclines molecules. Then the receptor was used as recognition reagent to develop a direct competitive enzyme linked immunosorbent assay for determination of the 5 drugs in milk, and the light signal was induced with 4-(imidazol-1-yl)phenol enhanced luminol-HO system. The limits of detection for the 5 drugs in milk were in the range of 5-16 pg/mL, and the recoveries from the standards fortified blank milk were in the range of 71.7%-95.8%. Therefore, this method could be used as a simple, rapid, and ultra-sensitive tool to monitor the residues of tetracyclines in milk.

摘要

本研究首次报道了一种基于受体的化学发光免疫分析方法,用于分析四环素类药物。实验过程中,将 TetR 蛋白基因转化到 Rosetta-gami(DE3)中表达受体,并通过分子对接技术研究了其对 5 种四环素类药物的识别机制。结果表明,疏水相互作用和π-π键是 TetR-四环素类药物结合的主要分子间力,D 环是四环素类分子中受体的主要结合部位。然后,将受体用作识别试剂,开发了一种用于测定牛奶中 5 种药物的直接竞争酶联免疫吸附测定法,并使用 4-(咪唑-1-基)苯酚增强鲁米诺-HO 体系诱导光信号。该方法在牛奶中的 5 种药物的检测限范围为 5-16 pg/mL,标准添加空白牛奶的回收率范围为 71.7%-95.8%。因此,该方法可作为一种简单、快速、超灵敏的工具,用于监测牛奶中四环素类药物的残留。

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