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一种采用GloSensor技术的重组人脑利钠肽(rhBNP)快速报告基因检测法。

A rapid reporter assay for recombinant human brain natriuretic peptide (rhBNP) by GloSensor technology.

作者信息

Yu Lei, Shi Xinchang, Han Chunmei, Rao Chunming, Wang Junzhi

机构信息

National Institutes for Food and Drug Control, Beijing 100050, China.

WHO Collaboration Centre for Biologicals Standardization and Evaluation, Beijing 100050, China.

出版信息

J Pharm Anal. 2018 Oct;8(5):297-301. doi: 10.1016/j.jpha.2018.04.003. Epub 2018 Apr 20.

Abstract

Accurate determination of biological activity is essential in quality control of recombinant human brain natriuretic peptide (rhBNP). In previous study, we successfully developed a genetically modified cell line 293GCAC3-based ELISA assay for rhBNP. But ELISA procedure is still tedious, so this study was aimed to develop a rapid and simple bioassay for rhBNP using GloSensor technology, which provides a platform of flexible luciferase-based biosensors for real-time detection of signaling events in live cells, including cGMP production. A reporter cell line 293GCAGlo-G1 was constructed by transfecting pGloSensor™ 40 F plasmid into 293GCAC3. The reporter assay based on 293GCAGlo-G1 showed high precision with intra-assay CV being 8.3% and inter-assay CV being 14.1%; high accuracy with 80%, 100% and 120% recovery rate being 99.2%, 102.4% and 99.0% respectively; and great linearity with R of linear fitting equation being 0.99. Besides, no significant difference was found in test results of reporter assay and 293GCAC3-based ELISA assay (paired test,  = 0.630). All these results suggested that the reporter assay was a viable assay for biological determination of rhBNP.

摘要

准确测定生物活性对于重组人脑利钠肽(rhBNP)的质量控制至关重要。在先前的研究中,我们成功开发了基于基因改造细胞系293GCAC3的rhBNP ELISA检测方法。但ELISA检测过程仍然繁琐,因此本研究旨在利用GloSensor技术开发一种快速简便的rhBNP生物检测方法,该技术提供了一个基于荧光素酶的灵活生物传感器平台,用于实时检测活细胞中的信号事件,包括cGMP的产生。通过将pGloSensor™ 40 F质粒转染到293GCAC3中构建了报告细胞系293GCAGlo-G1。基于293GCAGlo-G1的报告基因检测显示出高精度,批内变异系数为8.3%,批间变异系数为14.1%;高准确度,80%、100%和120%回收率分别为99.2%、102.4%和99.0%;以及良好的线性,线性拟合方程的R为0.99。此外,报告基因检测和基于293GCAC3的ELISA检测的结果没有显著差异(配对检验,P = 0.630)。所有这些结果表明,报告基因检测是一种可行的rhBNP生物学测定方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dc7/6190497/7a5ff5c9d133/gr1.jpg

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