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以外源碱基为导向——通过体外转录对大型功能性RNA进行位点特异性环丙烯修饰的策略

Iluminated by foreign letters - Strategies for site-specific cyclopropene modification of large functional RNAs via in vitro transcription.

作者信息

Eggert Frank, Kulikov Katharina, Domnick Christof, Leifels Philipp, Kath-Schorr Stephanie

机构信息

LIMES Institute, Chemical Biology & Medicinal Chemistry Unit, University of Bonn, Gerhard-Domagk-Straße 1, 53121 Bonn, Germany.

LIMES Institute, Chemical Biology & Medicinal Chemistry Unit, University of Bonn, Gerhard-Domagk-Straße 1, 53121 Bonn, Germany.

出版信息

Methods. 2017 May 1;120:17-27. doi: 10.1016/j.ymeth.2017.04.021. Epub 2017 Apr 26.

DOI:10.1016/j.ymeth.2017.04.021
PMID:28454775
Abstract

The synthesis of sequence-specifically modified long RNA molecules, which cannot entirely be prepared via solid phase synthesis methods is experimentally challenging. We are using a new approach based on an expanded genetic alphabet preparing site-specifically modified RNA molecules via standard in vitro transcription. In this report, the site-specific labeling of functional RNAs, in particular ribozymes and a long non-coding RNA with cyclopropene moieties, is presented. We provide detailed instructions for RNA labeling via in vitro transcription and include required analytical methods to verify production and identity of the transcript. We further present post-transcriptional inverse electron demand Diels-Alder cycloaddition reactions on the cyclopropene-modified sequences and discuss applications of the genetic alphabet expansion transcription for in vitro preparation of labeled functional RNAs with complex foldings. In detail, the glmS and CPEB3 ribozymes were site-specifically decorated with methyl cyclopropene moieties using the unnatural TPT3 triphosphate and were proven to be still functional. In addition, the structurally complex A region of the Xist lncRNA (401nt) was site-specifically modified with methyl cyclopropene and detected by fluorescence after cycloaddition reaction with a tetrazine-BODIPY conjugate.

摘要

合成序列特异性修饰的长RNA分子在实验上具有挑战性,因为无法完全通过固相合成方法来制备。我们正在使用一种基于扩展遗传字母表的新方法,通过标准的体外转录来制备位点特异性修饰的RNA分子。在本报告中,展示了功能性RNA的位点特异性标记,特别是具有环丙烯部分的核酶和长链非编码RNA。我们提供了通过体外转录进行RNA标记的详细说明,并包括验证转录本的产生和身份所需的分析方法。我们还展示了在环丙烯修饰序列上的转录后逆电子需求狄尔斯-阿尔德环加成反应,并讨论了遗传字母表扩展转录在体外制备具有复杂折叠的标记功能性RNA中的应用。具体而言,使用非天然的TPT3三磷酸将甲基环丙烯部分位点特异性地修饰到glmS和CPEB3核酶上,并证明它们仍然具有功能。此外,Xist长链非编码RNA(401nt)结构复杂的A区域用甲基环丙烯进行了位点特异性修饰,并在与四嗪-硼二吡咯共轭物发生环加成反应后通过荧光检测到。

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