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钴(III)多吡啶配合物与DNA相互作用的研究:实验与计算方法

Study of the interaction of Co(III) polypyridyl complexes with DNA: an experimental and computational approach.

作者信息

Nambagari Navaneetha, Perka Shyam, Vuradi Ravi Kumar, Satyanarayana S

机构信息

a Department of Chemistry , University College of Science, Osmania University , Hyderabad , India.

出版信息

Nucleosides Nucleotides Nucleic Acids. 2019;38(6):400-417. doi: 10.1080/15257770.2018.1554222. Epub 2019 Jan 28.

DOI:10.1080/15257770.2018.1554222
PMID:30689503
Abstract

Three new cobalt(III) polypyridyl complexes, [Co(L - L)IIP] where IIP = 2-(2H-isoindol-1-yl)-2H-imidazo[4,5-f][1, 10]phenanthroline, L = 1) phen (1,10-phenanthroline), 2) bpy (2,2'bipyridyl), 3) dmb (4, 4-dimethyl 2, 2'-bipyridine) have been synthesized, characterized (UV -VIS, IR, HNMR and C NMR spectroscopy) and screened for their in vitro antibacterial activity against E.coli, Staphylococcus aureus and Bacillus subtilis. The binding of these complexes with calf-thymus DNA (CT-DNA) has been investigated by absorption and fluorescence spectroscopy, viscosity measurements. The experimental studies indicate that complexes bind to CT-DNA by means of intercalation, but with different binding affinities due to differences in the planarity of the ancillary ligand. The complexes promote photocleavage of plasmid DNA from super coiled form I to the open circular form II. The antibacterial activities suggest that the metal complexes are more active as compared to the prepared un-complexed IIP ligand. In addition, a conformational search was carried out by Molecular Dynamics Simulations, and docking revealed that complexes intercalate between base pairs of DNA. The experimental and computational approaches reveal that the length of the intercalator and the nature of ancillary ligand are highly important factors for DNA binding.

摘要

合成了三种新型钴(III)多吡啶配合物,即[Co(L - L)IIP],其中IIP = 2-(2H-异吲哚-1-基)-2H-咪唑并[4,5-f][1,10]菲咯啉,L分别为:1)phen(1,10-菲咯啉)、2)bpy(2,2'-联吡啶)、3)dmb(4,4-二甲基2,2'-联吡啶)。对其进行了表征(紫外可见光谱、红外光谱、核磁共振氢谱和碳谱),并筛选了它们对大肠杆菌、金黄色葡萄球菌和枯草芽孢杆菌的体外抗菌活性。通过吸收光谱、荧光光谱和粘度测量研究了这些配合物与小牛胸腺DNA(CT-DNA)的结合情况。实验研究表明,配合物通过嵌入作用与CT-DNA结合,但由于辅助配体平面性的差异,结合亲和力不同。这些配合物可促进质粒DNA从超螺旋形式I光裂解为开环形式II。抗菌活性表明,与制备的未络合IIP配体相比,金属配合物的活性更高。此外,通过分子动力学模拟进行了构象搜索,对接结果显示配合物嵌入DNA的碱基对之间。实验和计算方法表明,嵌入剂的长度和辅助配体的性质是影响DNA结合的重要因素。

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