Xue-Wen Huang, Jie Pan, Xian-Yuan An, Hong-Xiang Zhuge
Department of pathogenic organisms, Preclinical medicine college, Suzhou university, Suzhou 215123, China.
J Pept Sci. 2007 Apr;13(4):220-6. doi: 10.1002/psc.835.
The objective of this work was to study the inhibitory effects of antisense peptide nucleic acids (PNAs) targeted to domain II of 23S rRNA on bacterial translation and growth. In this paper, we report that PNA(G1138) or peptide-PNA(G1138) targeted to domain II of 23S rRNA can inhibit both translation in vitro (in a cell-free translation system) and bacterial growth in vivo. The inhibitory concentration (IC50) and the minimum inhibiting concentration (MIC) are 0.15 and 10 microM, respectively. The inhibition effect of PNA(G1138) in vitro is somewhat lower than that of tetracycline (IC50 = 0.12 microM), but the MIC of peptide-PNA(G1138) against Escherichia coli is significantly higher than that of tetracycline (MIC = 4 microM). Further studies based on similar colony-forming unit (CFU) assays showed that peptide-PNA(G1138) at 10 microM is bactericidal, but the bactericidal effect is less effective than that of tetracycline. Nevertheless, the results demonstrated that the peptide-PNA(G1138) treatment is bactericidal in a dose- and sequence-dependent manner and that the G1138 site of 23S rRNA is a possible sequence target for designing novel PNA-based antibiotics.
本研究的目的是探讨针对23S rRNA结构域II的反义肽核酸(PNA)对细菌翻译和生长的抑制作用。在本文中,我们报道了靶向23S rRNA结构域II的PNA(G1138)或肽-PNA(G1138)既能在体外(无细胞翻译系统中)抑制翻译,也能在体内抑制细菌生长。抑制浓度(IC50)和最小抑制浓度(MIC)分别为0.15和10 microM。PNA(G1138)在体外的抑制作用略低于四环素(IC50 = 0.12 microM),但肽-PNA(G1138)对大肠杆菌的MIC显著高于四环素(MIC = 4 microM)。基于类似菌落形成单位(CFU)测定的进一步研究表明,10 microM的肽-PNA(G1138)具有杀菌作用,但其杀菌效果不如四环素。然而,结果表明肽-PNA(G1138)处理具有剂量和序列依赖性杀菌作用,且23S rRNA的G1138位点是设计新型基于PNA的抗生素的可能序列靶点。