Pei Renjun, Rothman Jeffrey, Xie Yuli, Stojanovic Milan N
Division of Experimental Therapeutics, Department of Medicine, Columbia University, New York, NY 10032, USA.
Nucleic Acids Res. 2009 May;37(8):e59. doi: 10.1093/nar/gkp154. Epub 2009 Mar 17.
The full understanding of dynamics of cellular processes hinges on the development of efficient and non-invasive labels for intracellular RNA species. Light-up aptamers binding fluorogenic ligands show promise as specific labels for RNA species containing those aptamers. Herein, we took advantage of existing, non-light-up aptamers against small molecules and demonstrated a new class of light-up probes in vitro. We synthesized two conjugates of thiazole orange dye to small molecules (GMP and AMP) and characterized in vitro their interactions with corresponding RNA aptamers. The conjugates preserved specific binding to aptamers while showing several 100-fold increase in fluorescence of the dye (the 'light-up' property). In the presence of free small molecules, conjugates can be displaced from aptamers serving also as fluorescent sensors. Our in vitro results provide the proof-of-concept that the small-molecule conjugates with light-up properties can serve as a general approach to label RNA sequences containing aptamers.
对细胞过程动力学的全面理解取决于能否开发出针对细胞内RNA种类的高效且非侵入性的标记物。与荧光配体结合的点亮型适配体有望作为含有这些适配体的RNA种类的特异性标记物。在此,我们利用现有的针对小分子的非点亮型适配体,在体外展示了一类新型的点亮型探针。我们合成了噻唑橙染料与小分子(鸟苷酸和腺苷酸)的两种缀合物,并在体外表征了它们与相应RNA适配体的相互作用。这些缀合物保留了与适配体的特异性结合,同时染料的荧光增强了数百倍(即“点亮”特性)。在存在游离小分子的情况下,缀合物可从适配体上被置换下来,这也使它们可作为荧光传感器。我们的体外研究结果提供了概念验证,即具有点亮特性的小分子缀合物可作为标记含有适配体的RNA序列的通用方法。