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Inhibition of translation and bacterial growth by peptide nucleic acid targeted to ribosomal RNA

机译:靶向核糖体RNA的肽核酸抑制翻译和细菌生长

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摘要

Peptide nucleic acid (PNA) is a DNA mimic that has shown considerable promise as a lead compound for developing gene therapeutic drugs. We report that PNAs targeted to functional and accessible sites in ribosomal RNA can inhibit translation in an Escherichia coli cell-free transcription/translation system, with 50% reductions caused by nanomolar PNA concentrations. The effect in vitro is quantitatively similar to that of the known translation inhibitor and antibiotic tetracycline. Also, the targeted PNAs inhibited bacterial growth on agar plates and in liquid culture. A strain of E. coli (AS19) that is more permeable to antibiotics was approximately 10-fold more sensitive to the active PNAs, suggesting that the effect on growth indeed was caused by PNAs that entered cells. Inhibition was not observed when using control PNAs of similar composition but with an unrelated or mismatched sequence. The results demonstrate that ribosomal RNA is a possible target for sequence-designed novel antibiotics based on DNA analogues or mimics.
机译:肽核酸(PNA)是一种DNA模仿物,作为开发基因治疗药物的先导化合物具有广阔的前景。我们报告说,针对核糖体RNA中的功能性和可及性位点的PNA可以抑制大肠杆菌无细胞转录/翻译系统中的翻译,而纳摩尔PNA浓度降低了50%。体外作用在数量上类似于已知翻译抑制剂和抗生素四环素的作用。而且,靶向的PNA抑制了琼脂平板和液体培养中的细菌生长。对抗生素更具渗透性的大肠杆菌(AS19)菌株对活性PNA的敏感性大约高10倍,这表明对生长的影响确实是由进入细胞的PNA引起的。当使用相似组成但序列不相关或错配的对照PNA时,未观察到抑制作用。结果表明,核糖体RNA是基于DNA类似物或模拟物进行序列设计的新型抗生素的可能靶标。

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