Indian Institute of Science Education and Research, Sai Trinity Building, Pashan, Pune 411021, India.
Chem Commun (Camb). 2012 Jan 14;48(4):498-500. doi: 10.1039/c1cc15659d. Epub 2011 Oct 17.
Direct incorporation of azide groups into RNA oligonucleotides by in vitro transcription reactions in the presence of a new azide-modified UTP analogue, and subsequent posttranscriptional chemical labeling of azide-modified oligoribonucleotide transcripts by click and Staudinger reactions are described. This postsynthetic labeling protocol is robust and modular, and offers an alternative access to RNA labeled with biophysical probes.
通过在体外转录反应中加入一种新的叠氮修饰的 UTP 类似物,将叠氮基团直接引入 RNA 寡核苷酸中,随后通过点击反应和施蒂德反应对转录后的叠氮修饰寡核糖核苷酸进行化学标记,描述了这一过程。这种合成后标记的方案具有稳健性和模块化的特点,为带有生物物理探针的 RNA 提供了另一种标记方法。