Bessler Larissa, Groß Jonathan, Kampf Christopher J, Opatz Till, Helm Mark
Institute of Pharmaceutical and Biomedical Sciences, Johannes Gutenberg University Mainz Staudingerweg 5 55128 Mainz Germany
Department of Chemistry, Johannes Gutenberg University Mainz Duesbergweg 10-14 55128 Mainz Germany.
RSC Chem Biol. 2024 Feb 1;5(3):216-224. doi: 10.1039/d3cb00221g. eCollection 2024 Mar 6.
The occurrence of non-canonical nucleoside structures in RNA of biological or synthetic origin has encountered several recent boosts in attention, namely in the context of RNA modifications, and with an eye to RNA vaccines. New nucleoside structures introduce added functionality and function into biopolymers that are otherwise rather homogenous in their chemical structure. Here, we report the discovery of a presumed RNA modification that was identified by combination of liquid chromatography-tandem mass spectrometry (LC-MS/MS) with stable isotope labelling as a dimer of the known RNA modification 4-thiouridine (sU). The disulfide-linked structure, which had previously been synthetically introduced into RNA, was here formed spontaneously in isolates of tRNA. Judicious application of stable isotope labelling suggested that this presumed new RNA modification was rather generated by oxidation with ambient oxygen. These findings do not only underscore the need for caution in the discovery of new RNA modifications with respect to artifacts, but also raise awareness of an RNA vulnerability, especially to oxidative damage, during its transport or storage.
生物或合成来源的RNA中非经典核苷结构的出现,最近在几个方面受到了更多关注,即在RNA修饰的背景下,以及着眼于RNA疫苗。新的核苷结构为化学结构原本相当单一的生物聚合物引入了额外的功能。在这里,我们报告了一种推测的RNA修饰的发现,它是通过液相色谱-串联质谱(LC-MS/MS)与稳定同位素标记相结合而鉴定出来的,是已知RNA修饰4-硫尿苷(sU)的二聚体。这种二硫键连接的结构,此前已被人工引入RNA中,在这里是在tRNA分离物中自发形成的。稳定同位素标记的明智应用表明,这种推测的新RNA修饰相当可能是由环境中的氧气氧化产生的。这些发现不仅强调了在发现新的RNA修饰时要警惕人为假象,也提高了人们对RNA在运输或储存过程中,尤其是对氧化损伤的脆弱性的认识。