Michelini Elisa, Cevenini Luca, Mezzanotte Laura, Leskinen Piia, Virta Marko, Karp Matti, Roda Aldo
Department of Pharmaceutical Sciences, University of Bologna, via Belmeloro 6, 40126 Bologna, Italy.
Nat Protoc. 2008;3(12):1895-902. doi: 10.1038/nprot.2008.189.
We report a step-by-step protocol describing how to develop and use a yeast-based bioassay for androgen-like compounds. Saccharomyces cerevisiae cells are genetically engineered to express the human androgen receptor (hAR) and the bioluminescent (BL) reporter gene luciferase (from Photinus pyralis) under the control of the androgen response element (ARE). In the presence of androgens, activated hAR binds to the ARE sequences and activates luciferase expression. After addition of D-luciferin, luciferase activity measurements can be performed, and the BL signal is proportional to the androgenic activity of the sample. Cytotoxic effects of the sample are monitored by the use of a control yeast strain that allows BL signal correction according to cell viability. After overnight culture of the recombinant strain, the assay can be accomplished in a 96-well microplate format in 1 working day with a detection limit of 0.05 nM for testosterone and intra- and interassay variability of 14% and 23%, respectively.
我们报告了一个详细的实验方案,描述了如何开发和使用基于酵母的雄激素样化合物生物测定法。酿酒酵母细胞经过基因工程改造,以在雄激素反应元件(ARE)的控制下表达人雄激素受体(hAR)和生物发光(BL)报告基因荧光素酶(来自萤火虫)。在雄激素存在的情况下,活化的hAR与ARE序列结合并激活荧光素酶表达。加入D-荧光素后,可以进行荧光素酶活性测量,并且BL信号与样品的雄激素活性成正比。通过使用对照酵母菌株监测样品的细胞毒性作用,该对照酵母菌株可根据细胞活力对BL信号进行校正。重组菌株过夜培养后,该测定可在96孔微孔板中于1个工作日内完成,睾酮的检测限为0.05 nM,测定内和测定间的变异分别为14%和23%。