Bornewasser Lisa, Domnick Christof, Kath-Schorr Stephanie
Institute of Organic Chemistry, Department of Chemistry, University of Cologne Greinstrasse 4 50939 Cologne Germany
Chem Sci. 2022 Mar 3;13(17):4753-4761. doi: 10.1039/d2sc00670g. eCollection 2022 May 4.
The preparation of highly modified mRNAs and visualization of their cellular distribution are challenging. We report in-cell application of transcribed mRNA containing natural base modifications and site-specifically introduced artificial nucleotides. Click chemistry on mRNA allows visualization in cells with excellent signal intensities. While non-specific introduction of reporter groups often leads to loss in mRNA functionality, we combined the benefits from site-specificity in the 3'-UTR incorporated unnatural nucleotides with the improved translation efficiency of the natural base modifications Ψ and 5mC. A series of experiments is described to observe, quantify and verify mRNA functionality. This approach represents a new way to visualize mRNA delivery into cells and monitor its spread on a cellular level and translation efficiency. We observed increased protein expression from this twofold chemically modified, artificial mRNA counterbalancing a reduced transfection rate. This synergetic effect can be exploited as a powerful tool for future research on mRNA therapeutics.
高度修饰的mRNA的制备及其细胞分布的可视化具有挑战性。我们报告了含有天然碱基修饰和位点特异性引入的人工核苷酸的转录mRNA的细胞内应用。mRNA上的点击化学可在细胞中实现具有出色信号强度的可视化。虽然报告基团的非特异性引入通常会导致mRNA功能丧失,但我们将3'-UTR中掺入非天然核苷酸的位点特异性优势与天然碱基修饰Ψ和5mC提高的翻译效率相结合。描述了一系列实验以观察、量化和验证mRNA的功能。这种方法代表了一种可视化mRNA递送至细胞并在细胞水平上监测其扩散和翻译效率的新方法。我们观察到这种经过双重化学修饰的人工mRNA的蛋白质表达增加,抵消了转染率的降低。这种协同效应可作为未来mRNA治疗研究的有力工具。