Yu Lei, Shi Xinchang, Han Chunmei, Rao Chunming, Wang Junzhi
National Institutes for Food and Drug Control, Beijing 100050, China.
WHO Collaboration Centre for Biologicals Standardization and Evaluation, Beijing 100050, China.
J Pharm Anal. 2018 Oct;8(5):297-301. doi: 10.1016/j.jpha.2018.04.003. Epub 2018 Apr 20.
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.
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。