Live cell imaging of single RNA molecules with fluorogenic Mango II arrays

被引:106
作者
Cawte, Adam D. [1 ,2 ]
Unrau, Peter J. [3 ]
Rueda, David S. [1 ,2 ]
机构
[1] MRC London Inst Med Sci, Single Mol Imaging Grp, Du Cane Rd, London, England
[2] Imperial Coll London, Dept Infect Dis, Fac Med, Du Cane Rd, London, England
[3] Simon Fraser Univ, Dept Mol Biol & Biochem, 8888 Univ Dr, Burnaby, BC, Canada
基金
英国惠康基金; 英国医学研究理事会; 加拿大自然科学与工程研究理事会;
关键词
MESSENGER-RNAS; IN-VIVO; SUPERRESOLUTION MICROSCOPY; TRANSLATION DYNAMICS; GENE-EXPRESSION; LOCALIZATION; FLUORESCENCE; TRANSCRIPTS; FLUOROPHORE; REVEALS;
D O I
10.1038/s41467-020-14932-7
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
RNA molecules play vital roles in many cellular processes. Visualising their dynamics in live cells at single-molecule resolution is essential to elucidate their role in RNA metabolism. RNA aptamers, such as Spinach and Mango, have recently emerged as a powerful background-free technology for live-cell RNA imaging due to their fluorogenic properties upon ligand binding. Here, we report a novel array of Mango II aptamers for RNA imaging in live and fixed cells with high contrast and single-molecule sensitivity. Direct comparison of Mango II and MS2-tdMCP-mCherry dual-labelled mRNAs show marked improvements in signal to noise ratio using the fluorogenic Mango aptamers. Using both coding (beta-actin mRNA) and long non-coding (NEAT1) RNAs, we show that the Mango array does not affect cellular localisation. Additionally, we can track single mRNAs for extended time periods, likely due to bleached fluorophore replacement. This property makes the arrays readily compatible with structured illumination super-resolution microscopy.
引用
收藏
页数:11
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