Sunbul Murat, Arora Ankita, Jäschke Andres
Institute of Pharmacy and Molecular Biotechnology, Heidelberg University, Im Neuenheimer Feld 364, Heidelberg, 69120, Germany.
Methods Mol Biol. 2018;1649:289-304. doi: 10.1007/978-1-4939-7213-5_19.
To elucidate the roles, dynamics, and regulation of RNAs, it is vital to be able to visualize the RNA of interest (ROI) in living cells noninvasively. Here, we describe a novel live-cell RNA imaging method using fluorophore- and quencher-binding aptamers, which can be genetically fused to the ROI. In this method, new membrane permeable and nonfluorescent fluorophore-quencher conjugates were utilized, and we showed that their fluorescence increases dramatically upon binding to fluorophore- or quencher-binding aptamers. This phenomenon allowed for labeling the ROI with many different colored fluorophores and also dual-color imaging of two distinct RNAs in live bacteria. Our approach uses small RNA tags and small molecule fluorophores for labeling, thereby minimal perturbation on the function and dynamics of the RNA of interest is expected.
为了阐明RNA的作用、动态变化及调控机制,能够在活细胞中以非侵入性方式可视化目标RNA(ROI)至关重要。在此,我们描述了一种使用荧光团和猝灭剂结合适体的新型活细胞RNA成像方法,该适体可与目标RNA进行基因融合。在这种方法中,使用了新型的可透过细胞膜的非荧光荧光团 - 猝灭剂共轭物,并且我们证明它们在与荧光团或猝灭剂结合适体结合后荧光会显著增加。这种现象使得能够用许多不同颜色的荧光团标记目标RNA,还能对活细菌中的两种不同RNA进行双色成像。我们的方法使用小RNA标签和小分子荧光团进行标记,因此预计对目标RNA的功能和动态变化的干扰最小。