Department of Chemistry "G. Ciamician", University of Bologna, Via Selmi 2, 40126, Bologna, Italy.
Department of Biological Geological and Environmental Sciences (BIGeA), University of Bologna, Via Irnerio 42, 40126, Bologna, Italy.
Anal Bioanal Chem. 2019 Jul;411(19):4937-4949. doi: 10.1007/s00216-019-01805-2. Epub 2019 Apr 10.
Cell-based assays utilizing reporter gene technology have been widely exploited for biosensing, as they provide useful information about the bioavailability and cell toxicity of target analytes. The long assay time due to gene transcription and translation is one of the main drawbacks of cell biosensors. We report the development of two yeast biosensors stably expressing human estrogen receptors α and β and employing NanoLuc as the reporter protein to upgrade the widely used yeast estrogen screening (YES) assays. A viability control strain was also developed based on a chimeric green-emitting luciferase, PLG2, expressed for the first time in Saccharomycescerevisiae. Thanks to their brightness, NanoLuc and PLG2 provided excellent sensitivity, enabling the implementation of these biosensors into low-cost smartphone-based devices. The developed biosensors had a rapid (1 h) response and reported on (anti)estrogenic activity via human estrogen receptors α and β as well as general sample toxicity. Under optimized conditions, we obtained LODs of 7.1 ± 0.4 nM and 0.38 ± 0.08 nM for E2 with nanoYESα and nanoYESβ, respectively. As a proof of concept, we analyzed real samples from plants showing significant estrogenic activity or known to contain significant amounts of phytoestrogens. Graphical abstract.
基于报告基因技术的细胞分析已被广泛用于生物传感,因为它们可以提供有关目标分析物生物利用度和细胞毒性的有用信息。由于基因转录和翻译,长的测定时间是细胞生物传感器的主要缺点之一。我们报告了两种稳定表达人雌激素受体 α 和 β 的酵母生物传感器的开发,并采用 NanoLuc 作为报告蛋白,对广泛使用的酵母雌激素筛选 (YES) 测定进行升级。还根据首次在酿酒酵母中表达的嵌合绿色发光酶 PLG2 开发了一种基于细胞活力的对照菌株。由于其亮度,NanoLuc 和 PLG2 提供了极好的灵敏度,使这些生物传感器能够集成到低成本的智能手机设备中。开发的生物传感器具有快速(1 小时)的响应,并通过人雌激素受体 α 和 β 以及一般样品毒性报告(抗)雌激素活性。在优化条件下,我们分别用 nanoYESα 和 nanoYESβ 获得了 E2 的 LOD 分别为 7.1±0.4 nM 和 0.38±0.08 nM。作为概念验证,我们分析了来自具有显著雌激素活性的植物或已知含有大量植物雌激素的真实样本。