Strack Rita L, Keenan Robert J, Glick Benjamin S
Department of Biochemistry and Molecular Biology, Gordon Center for Integrated Sciences, The University of Chicago, Chicago, IL, USA.
Methods Mol Biol. 2011;699:355-70. doi: 10.1007/978-1-61737-950-5_17.
Fluorescent proteins (FPs) are invaluable tools for biomedical research. Useful FPs have desirable fluorescence properties such as brightness and photostability, but a limitation is that many orange, red, and far-red FPs are cytotoxic when expressed in the cytosol. This cytotoxicity stems from aggregation. To reduce aggregation, we engineered the surface of DsRed-Express to generate DsRed-Express2, a highly soluble tetrameric FP that is noncytotoxic in bacterial and mammalian cells. Directed evolution of DsRed-Express2 yielded the color variants E2-Orange, E2-Red/Green, and E2-Crimson. These variants can be used to label whole cells for single- and multi-color experiments employing microscopy or flow cytometry. Methods are described for reducing the higher-order aggregation of oligomeric FPs and for analyzing FP cytotoxicity in Escherichia coli and HeLa cells.
荧光蛋白(FPs)是生物医学研究中非常有价值的工具。有用的荧光蛋白具有诸如亮度和光稳定性等理想的荧光特性,但一个局限性在于,许多橙色、红色和远红色荧光蛋白在胞质溶胶中表达时具有细胞毒性。这种细胞毒性源于聚集。为了减少聚集,我们对DsRed-Express的表面进行了改造,以生成DsRed-Express2,这是一种高度可溶的四聚体荧光蛋白,在细菌和哺乳动物细胞中无细胞毒性。对DsRed-Express2进行定向进化产生了颜色变体E2-橙色、E2-红/绿和E2-深红色。这些变体可用于标记完整细胞,用于采用显微镜或流式细胞术的单色和多色实验。本文描述了减少寡聚荧光蛋白高阶聚集以及分析大肠杆菌和HeLa细胞中荧光蛋白细胞毒性的方法。