Department of Chemistry and Biochemistry , University of California, San Diego , 9500 Gilman Drive , La Jolla , California 92093 , United States.
Mol Pharm. 2018 Mar 5;15(3):737-742. doi: 10.1021/acs.molpharmaceut.7b00356. Epub 2017 Aug 15.
Modified mRNA (mod-mRNA) has recently been widely studied as the form of RNA useful for therapeutic applications due to its high stability and lowered immune response. Herein, we extend the scope of the recently established RNA-TAG (transglycosylation at guanosine) methodology, a novel approach for genetically encoded site-specific labeling of large mRNA transcripts, by employing mod-mRNA as substrate. As a proof of concept, we covalently attached a fluorescent probe to mCherry encoding mod-mRNA transcripts bearing 5-methylcytidine and/or pseudouridine substitutions with high labeling efficiencies. To provide a versatile labeling methodology with a wide range of possible applications, we employed a two-step strategy for functionalization of the mod-mRNA to highlight the therapeutic potential of this new methodology. We envision that this novel and facile labeling methodology of mod-RNA will have great potential in decorating both coding and noncoding therapeutic RNAs with a variety of diagnostic and functional moieties.
修饰后的 mRNA(mod-mRNA)由于其高稳定性和降低的免疫反应,最近已被广泛研究为用于治疗应用的 RNA 形式。在此,我们通过使用 mod-mRNA 作为底物,扩展了最近建立的 RNA-TAG(鸟苷的转糖苷作用)方法的范围,这是一种用于对大型 mRNA 转录物进行基因编码的定点标记的新方法。作为概念验证,我们通过高标记效率将荧光探针共价连接到 mCherry 编码的 mod-mRNA 转录本上,这些转录本带有 5-甲基胞嘧啶和/或假尿嘧啶取代。为了提供一种具有广泛可能应用的多功能标记方法,我们采用两步策略对 mod-mRNA 进行功能化,以突出这种新方法的治疗潜力。我们设想,这种新型的 mod-RNA 简便标记方法将在对各种编码和非编码治疗性 RNA 进行修饰方面具有很大的潜力,可将各种诊断和功能部分与之结合。