Strategies for Covalent Labeling of Long RNAs

被引:35
作者
Depmeier, Hannah [1 ]
Hoffmann, Eva [1 ]
Bornewasser, Lisa [1 ]
Kath-Schorr, Stephanie [1 ]
机构
[1] Univ Cologne, Dept Chem, Greinstr 4, D-50939 Cologne, Germany
关键词
click chemistry; bioorthogonal labeling; lncRNA; ribozymes; RNA labeling; UNNATURAL BASE-PAIR; SITE-SPECIFIC INCORPORATION; ALPHABET EXPANSION TRANSCRIPTION; AZIDE-ALKYNE CYCLOADDITION; DIELS-ALDER REACTIONS; MESSENGER-RNA; ENZYMATIC INCORPORATION; GENETIC ALPHABET; CLICK CHEMISTRY; IN-VITRO;
D O I
10.1002/cbic.202100161
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The introduction of chemical modifications into long RNA molecules at specific positions for visualization, biophysical investigations, diagnostic and therapeutic applications still remains challenging. In this review, we present recent approaches for covalent internal labeling of long RNAs. Topics included are the assembly of large modified RNAs via enzymatic ligation of short synthetic oligonucleotides and synthetic biology approaches preparing site-specifically modified RNAs via in vitro transcription using an expanded genetic alphabet. Moreover, recent approaches to employ deoxyribozymes (DNAzymes) and ribozymes for RNA labeling and RNA methyltransferase based labeling strategies are presented. We discuss the potentials and limits of the individual methods, their applicability for RNAs with several hundred to thousands of nucleotides in length and indicate future directions in the field.
引用
收藏
页码:2826 / 2847
页数:22
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