Trachman Robert J, Truong Lynda, Ferré-D'Amaré Adrian R
Biochemistry and Biophysics Center, National Heart, Lung and Blood Institute, 50 South Drive MSC 8012, Bethesda, MD 20892-8012, USA.
Biochemistry and Biophysics Center, National Heart, Lung and Blood Institute, 50 South Drive MSC 8012, Bethesda, MD 20892-8012, USA.
Trends Pharmacol Sci. 2017 Oct;38(10):928-939. doi: 10.1016/j.tips.2017.06.007. Epub 2017 Jul 17.
Several aptamer RNAs have been selected in vitro that bind to otherwise weakly fluorescent small molecules and enhance their fluorescence several thousand-fold. By genetically tagging cellular RNAs of interest with these aptamers and soaking cells in their cell-permeable cognate small-molecule fluorophores, it is possible to use them to study RNA localization and trafficking. These aptamers have also been fused to metabolite-binding RNAs to generate fluorescent biosensors. The 3D structures of three unrelated fluorogenic RNAs have been determined, and reveal a shared reliance on base quadruples (tetrads) to constrain the photo-excited chromophore. The structural diversity of fluorogenic RNAs and the chemical diversity of potential fluorophores to be activated are likely to yield a variety of future fluorogenic RNA tags that are optimized for different applications in RNA imaging and in the design of fluorescent RNA biosensors.
已经在体外筛选出了几种适体RNA,它们能与原本荧光较弱的小分子结合,并将其荧光增强数千倍。通过用这些适体对感兴趣的细胞RNA进行基因标记,并将细胞浸泡在可透过细胞的同源小分子荧光团中,就可以用它们来研究RNA的定位和运输。这些适体还与代谢物结合RNA融合,以生成荧光生物传感器。已确定了三种不相关的荧光RNA的三维结构,结果表明它们都依赖碱基四重体(四联体)来限制光激发的发色团。荧光RNA的结构多样性以及待激活的潜在荧光团的化学多样性,可能会产生各种未来的荧光RNA标签,这些标签针对RNA成像和荧光RNA生物传感器设计中的不同应用进行了优化。