Enzyme-mediated tagging of RNA

被引:22
作者
Anhaeuser, Lea [1 ]
Rentmeistert, Andrea [1 ,2 ]
机构
[1] Univ Munster, Dept Chem, Inst Biochem, Wilhelm Klemm Str 2, D-48149 Munster, Germany
[2] Univ Munster, Cells In Mot Cluster Excellence CiM EXC1003, Munster, Germany
关键词
POSTTRANSCRIPTIONAL CHEMICAL FUNCTIONALIZATION; CLICK CHEMISTRY; MESSENGER-RNA; GENETIC ALPHABET; UNNATURAL BASE; LIVING CELLS; BIOORTHOGONAL REACTIONS; MOLECULAR BEACONS; NUCLEIC-ACIDS; UTP ANALOG;
D O I
10.1016/j.copbio.2017.03.013
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
RNA molecules can play diverse roles in the cell owing to their secondary structure dynamics and various binding modes. Studying localization and dynamics of RNA in vitro or in cells requires tagging with suitable reporter molecules fluorophores being the most prominent ones. Enzymatic RNA labeling approaches are currently emerging as valuable alternatives to purely chemical synthesis and to binding-or hybridization-based RNA-imaging approaches. Different classes of enzymes allow for cotranscriptional or posttranscriptional installation of small functional groups in RNA. The enzymatic step is typically combined with a second chemical step, providing flexibility regarding the reporter. The flourishing field of bioorthogonal chemistry propels this approach. We will present latest achievements and remaining challenges in the field of enzyme-mediated RNA tagging and emphasize efforts to achieve site-specificity and intracellular labeling.
引用
收藏
页码:69 / 76
页数:8
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