Division of Gene Regulation, Oncode Institute, the Netherlands Cancer Institute, 1066 CX Amsterdam, the Netherlands.
STAR Protoc. 2020 Oct 17;1(3):100142. doi: 10.1016/j.xpro.2020.100142. eCollection 2020 Dec 18.
This protocol describes how to image fluorescently tagged proteins, RNA, or DNA inside living cells at the single-molecule level. Imaging inside living cells, as opposed to fixed materials, gives access to real-time kinetic information. Although various single-molecule imaging applications are discussed, we focus on imaging of gene transcription at the single-RNA level. To obtain the best possible results, it is important that both imaging parameters and yeast culture conditions are optimized. Here, both aspects are described. For complete details on the use and execution of this protocol, please refer to Lenstra et al. (2015) and Donovan et al. (2019).
本方案描述了如何在活细胞内对荧光标记的蛋白质、RNA 或 DNA 进行单分子水平的成像。与固定材料相比,在活细胞内成像可以获得实时的动力学信息。虽然讨论了各种单分子成像应用,但我们重点介绍在单个 RNA 水平上对基因转录的成像。为了获得尽可能好的结果,优化成像参数和酵母培养条件非常重要。在这里,我们描述了这两个方面。有关本方案使用和执行的完整详细信息,请参见 Lenstra 等人(2015 年)和 Donovan 等人(2019 年)。