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Site-specific labeling of RNA by combining genetic alphabet expansion transcription and copper-free click chemistry

机译:通过结合遗传字母扩展转录和无铜点击化学技术对RNA进行位点特异性标记

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摘要

Site-specific labeling of long-chain RNAs with desired molecular probes is an imperative technique to facilitate studies of functional RNA molecules. By genetic alphabet expansion using an artificial third base pair, called an unnatural base pair, we present a post-transcriptional modification method for RNA transcripts containing an incorporated azide-linked unnatural base at specific positions, using a copper-free click reaction. The unnatural base pair between 7-(2-thienyl)imidazo[4,5-b]pyridine (Ds) and pyrrole-2-carbaldehyde (Pa) functions in transcription. Thus, we chemically synthesized a triphosphate substrate of 4-(4-azidopentyl)-pyrrole-2-carbaldehyde (N3-PaTP), which can be site-specifically introduced into RNA, opposite Ds in templates by T7 transcription. The N3-Pa incorporated in the transcripts was modified with dibenzocyclooctyne (DIBO) derivatives. We demonstrated the transcription of 17-, 76- and 260-mer RNA molecules and their site-specific labeling with Alexa 488, Alexa 594 and biotin. This method will be useful for preparing RNA molecules labeled with any functional groups of interest, toward in vivo experiments.
机译:用所需的分子探针对长链RNA进行位点特异性标记是一项促进研究功能性RNA分子的必不可少的技术。通过使用人工的第三碱基对(称为非天然碱基对)的遗传字母扩展,我们提出了一种利用无铜点击反应的RNA转录本的转录后修饰方法,该转录本在特定位置处包含掺入的叠氮化物连接的非天然碱基。 7-(2-噻吩基)咪唑并[4,5-b]吡啶(Ds)和吡咯-2-甲醛(Pa)之间的非天然碱基对在转录中起作用。因此,我们化学合成了4-(4-叠氮基戊基)-吡咯-2-甲醛(N 3 -PaTP)的三磷酸底物,该底物可以位点特异性地引入RNA中,与模板中的Ds相反通过T7转录。转录本中掺入的N 3 -Pa用二苯并环辛炔(DIBO)衍生物修饰。我们证明了17-,76-和260-mer RNA分子的转录以及Alexa 488,Alexa 594和生物素的位点特异性标记。对于体内实验,该方法可用于制备标记有任何目标功能基团的RNA分子。

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