Department of Medicinal Chemistry, University of Minnesota, 2231 6th Street SE, Minneapolis, MN 55455, USA.
Chemistry. 2022 Oct 18;28(58):e202201355. doi: 10.1002/chem.202201355. Epub 2022 Aug 25.
Catch and release DNA decoys (CRDDs) utilize photochemically responsive nucleoside analogues that generate abasic sites upon exposure to light. Herein, we describe the synthesis and evaluation of four candidate CRDD monomers containing nucleobases that mimic endogenous pyrimidines: 2-nitroimidazole (2-NI), 2-nitrobenzene (2-NB), 2-nitropyrrole (2-NP) and 3-nitropyrrole (3-NP). Our studies reveal that 2-NI and 2-NP can function as CRDDs, whereas 3-NP and 2-NB undergo decomposition and transformation to a higher-ordered structure upon photolysis, respectively. When incorporated into DNA, 2-NP undergoes rapid photochemical cleavage of the anomeric bond (1.8 min half-life) to yield an abasic site. Finally, we find that all four pyrimidine mimics show significantly greater stability when base-paired against the previously reported 7-nitroindole CRDD monomer. Our work marks the expansion of CRDD technology to both purine and pyrimidine scaffolds.
捕获并释放 DNA 诱饵(CRDDs)利用光响应性核苷类似物,这些类似物在暴露于光时会产生无碱基位点。在此,我们描述了四种含有模拟内源性嘧啶的碱基的候选 CRDD 单体的合成和评估:2-硝基咪唑(2-NI)、2-硝基苯(2-NB)、2-硝基吡咯(2-NP)和 3-硝基吡咯(3-NP)。我们的研究表明,2-NI 和 2-NP 可以作为 CRDD 发挥作用,而 3-NP 和 2-NB 在光解时分别分解并转化为更高级的结构。当掺入 DNA 时,2-NP 会迅速发生糖苷键的光化学断裂(半衰期为 1.8 分钟),产生无碱基位点。最后,我们发现所有四种嘧啶类似物与之前报道的 7-硝基吲哚 CRDD 单体配对时稳定性显著提高。我们的工作标志着 CRDD 技术扩展到嘌呤和嘧啶支架。