Li Dawei, Wang Qiang, Zhou Bing, Zhuge Qiang, Lv Bei
College of Biology and the Environment, Nanjing Forestry University 159 Longpan Road Nanjing 210037 China
The Southern Modern Forestry Collaborative Innovation Center, Nanjing Forestry University 159 Longpan Road Nanjing 210037 China.
RSC Adv. 2019 Jun 11;9(32):18415-18419. doi: 10.1039/c9ra02398d. eCollection 2019 Jun 10.
Bacterial topoisomerase I is a potential target during the course of antibacterial drug therapy. In our studies, specifically designed small DNA circles with high bending stress were synthesized. It is demonstrated that small DNA circles showed high inhibitory effect on the activity of bacterial topoisomerase I and the single-stranded regions associated with bending deformation in DNA circles are believed to be the crucial factor for trapping the enzymes and decreasing the effective concentration of the topoisomerases in the reaction solution. In addition, the DNA circles showed high thermal stability and excellent nuclease resistance. In consideration of the low cytotoxicity of DNA-based biopharmaceuticals, our results may provide a new idea for the future design and optimization of DNA-based therapeutic agents for antibacterial therapy.
细菌拓扑异构酶I是抗菌药物治疗过程中的一个潜在靶点。在我们的研究中,合成了具有高弯曲应力的特定设计的小DNA环。结果表明,小DNA环对细菌拓扑异构酶I的活性具有高度抑制作用,并且DNA环中与弯曲变形相关的单链区域被认为是捕获酶并降低反应溶液中拓扑异构酶有效浓度的关键因素。此外,DNA环表现出高热稳定性和优异的核酸酶抗性。鉴于基于DNA的生物药物的低细胞毒性,我们的结果可能为未来基于DNA的抗菌治疗药物的设计和优化提供新思路。