Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow 119991, Russia.
Emanuel Institute of Biochemical Physics, RAS, Moscow 119334, Russia.
Bioorg Med Chem. 2020 Apr 1;28(7):115378. doi: 10.1016/j.bmc.2020.115378. Epub 2020 Feb 13.
A set of AT-specific fluorescent dimeric bisbenzimidazoles DBPA(n) with linkers of different lengths bound to DNA in the minor groove were synthesized and their genetic, virological, and biochemical studies were performed. The DBPA(n) were shown to be effective inhibitors of the histon-like protein H-NS, a regulator of the DNA transcription factor, as well as of the Aliivibrio logei Quorum Sensing regulatory system in E. coli cells. Their antiviral activity was tested in model cell lines infected with herpes simplex virus type I. Also, it was found that DBPA(n) could inhibit catalytic activities of HIV-1 integrase at low micromolar concentrations. All of the dimeric bisbenzimidazoles DBPA(n) manifested fluorescent properties, were well soluble in water, nontoxic up to concentrations of 200 µM, and could penetrate into nuclei followed by binding to DNA.
一组具有不同长度连接体的 AT 特异性荧光二聚体双苯并咪唑 DBPA(n) 与 DNA 小沟中的 DNA 结合,对其进行了遗传、病毒学和生物化学研究。研究表明,DBPA(n) 是组蛋白样蛋白 H-NS 的有效抑制剂,H-NS 是 DNA 转录因子的调节剂,也是大肠杆菌细胞中 Aliivibrio logei Quorum Sensing 调节系统的调节剂。在感染单纯疱疹病毒 I 的模型细胞系中测试了它们的抗病毒活性。此外,还发现 DBPA(n) 可以在低微摩尔浓度下抑制 HIV-1 整合酶的催化活性。所有二聚体双苯并咪唑 DBPA(n) 都表现出荧光特性,在水中具有良好的溶解性,在高达 200 μM 的浓度下无毒性,并且可以穿透细胞核,然后与 DNA 结合。