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

机译:GloSensor技术用于重组人脑利钠肽(rhBNP)的快速报告基因检测

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摘要

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 R2 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 t test, p = 0.630). All these results suggested that the reporter assay was a viable assay for biological determination of rhBNP.
机译:准确测定生物学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修饰的293GCAC3细胞系的rhBNP ELISA分析。但是ELISA程序仍然繁琐,因此本研究旨在使用GloSensor技术开发一种用于rhBNP的快速,简单的生物测定方法,该技术为基于荧光素酶的灵活生物传感器平台提供了实时检测活细胞中信号事件(包括cGMP产生)的平台。 。通过将pGloSensor™40 F质粒转染到293GCAC3中来构建报告子细胞系293GCAGlo-G1。基于293GCAGlo-G1的报告基因检测具有很高的准确性,批内CV为8.3%,批间CV为14.1%。精度高,回收率分别为80%,100%和120%,分别为99.2%,102.4%和99.0%;线性拟合方程的R 2 具有很好的线性。此外,在报告基因检测和基于293GCAC3的ELISA检测(配对t检验,p = 0.630)的检测结果中没有发现显着差异。所有这些结果表明,报告基因测定是用于生物测定rhBNP的可行测定。

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