Vacek Jan, Zatloukalova Martina, Bartheldyova Eliska, Reha David, Minofar Babak, Bednarova Klara, Renciuk Daniel, Coufal Jan, Fojta Miroslav, Zadny Jaroslav, Gessini Alessandro, Rossi Barbara, Storch Jan, Kabelac Martin
Department of Medical Chemistry and Biochemistry, Faculty of Medicine and Dentistry, Palacky University, Hnevotinska 3, 775 15 Olomouc, Czech Republic.
Department of Medical Chemistry and Biochemistry, Faculty of Medicine and Dentistry, Palacky University, Hnevotinska 3, 775 15 Olomouc, Czech Republic.
Int J Biol Macromol. 2023 Oct 1;250:125905. doi: 10.1016/j.ijbiomac.2023.125905. Epub 2023 Jul 23.
In this contribution, we focused on a fundamental study targeting the interaction of water-soluble [6]helicene derivative 1 (1-butyl-3-(2-methyl[6]helicenyl)-imidazolium bromide) with double-stranded (ds) DNA. A synthetic 30-base pair duplex, plasmid, chromosomal calf thymus and salmon DNA were investigated using electrochemistry, electrophoresis and spectroscopic tools supported by molecular dynamics (MD) and quantum mechanical approaches. Both experimental and theoretical work revealed the minor groove binding of 1 to the dsDNA. Both the positively charged imidazole ring and hydrophobic part of the side chain contributed to the accommodation of 1 into the dsDNA structure. Neither intercalation into the duplex DNA nor the stable binding of 1 to single-stranded DNA were found in topoisomerase relaxation experiments with structural components of 1, i.e. [6]helicene (2) and 1-butyl-3-methylimidazolium bromide (3), nor by theoretical calculations. Finally, the binding of optically pure enantiomers (P)-1 and (M)-1 was studied using circular dichroism spectroscopy, isothermal titration calorimetry and UV Resonance Raman (UVRR) methods. Using MD and quantum mechanical methods, minor groove and semi-intercalation were proposed for compound 1 as the predominant binding modes. From the UVRR findings, we also can conclude that 1 tends to preferentially interact with adenine and guanine residues in the structure of dsDNA.
在本论文中,我们聚焦于一项基础研究,该研究旨在探讨水溶性[6]螺烯衍生物1(1-丁基-3-(2-甲基[6]螺烯基)-咪唑鎓溴化物)与双链(ds)DNA的相互作用。我们使用电化学、电泳和光谱学工具,并辅以分子动力学(MD)和量子力学方法,对合成的30碱基对双链体、质粒、染色体小牛胸腺DNA和鲑鱼DNA进行了研究。实验和理论工作均表明1与dsDNA存在小沟结合。带正电荷的咪唑环和侧链的疏水部分都有助于1嵌入dsDNA结构。在使用1的结构组分,即[6]螺烯(2)和1-丁基-3-甲基咪唑鎓溴化物(3)进行的拓扑异构酶松弛实验中,以及通过理论计算,均未发现1插入双链DNA或与单链DNA稳定结合的情况。最后,我们使用圆二色光谱、等温滴定量热法和紫外共振拉曼(UVRR)方法研究了光学纯对映体(P)-1和(M)-1的结合情况。使用MD和量子力学方法,我们提出化合物1的主要结合模式为小沟结合和半插入。根据UVRR的研究结果,我们还可以得出结论,1倾向于优先与dsDNA结构中的腺嘌呤和鸟嘌呤残基相互作用。