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首页> 外文期刊>Journal of Biomolecular Structure and Dynamics >Metal complexes of naphthoquinone based ligand: synthesis, characterization, protein binding, DNA binding/cleavage and cytotoxicity studies
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Metal complexes of naphthoquinone based ligand: synthesis, characterization, protein binding, DNA binding/cleavage and cytotoxicity studies

机译:基于萘醌的金属配合物的配体:合成,表征,蛋白质结合,DNA结合/切割和细胞毒性研究

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Protein binding, DNA binding/cleavage and in vitro cytotoxicity studies of 2-((3-(dimethylamino)propyl)amino)naphthalene-1,4-dione (L) and its four coordinated M(II) complexes [M(II) = Co(II), Cu(II), Ni(II) and Zn(II)] have been investigated using various spectral techniques. The structure of the ligand was confirmed by spectral and single crystal XRD studies. The geometry of the complexes has been established using analytical and spectral investigations. These complexes show good binding tendency to bovine serum albumin (BSA) exhibiting high binding constant values (10(5) M-1) when compared to free ligand. Fluorescence titration studies reveal that these compounds bind strongly with CT-DNA through intercalative mode (K-app 10(5) M-1) and follow the order: Cu(II) Zn(II) Ni(II) Co(II) L. Molecular docking study substantiate the strength and mode of binding of these compounds with DNA. All the complexes efficiently cleaved pUC18-DNA via hydroxyl radical mechanism and the Cu(II) complex degraded the DNA completely by converting supercoiled form to linear form. The complexes demonstrate a comparable in vitro cytotoxic activity against two human cancer cell lines (MCF-7 and A-549), which is comparable with that of cisplatin. AO/EB and DAPI staining studies suggest apoptotic mode of cell death, in these cancer cells, with the compounds under investigation.
机译:蛋白质结合,DNA结合/切割和体外细胞毒性研究的2 - ((3-(二甲基氨基)丙基)氨基)萘-1,4-二酮(L)及其四个配位M(II)配合物[M(II) = CO(II),使用各种光谱技术研究了Cu(II),Ni(II)和Zn(II)]。通过光谱和单晶XRD研究证实配体的结构。使用分析和光谱研究建立了复合物的几何形状。与游离配体相比,这些复合物对表现出高结合常数值(10(5)m-1)的牛血清白蛋白(BSA)具有良好的结合趋势。荧光滴定研究表明,这些化合物通过插入式模式(K-APP 10(5)M-1)与CT-DNA强烈粘合并遵循顺序:Cu(II)& Zn(ii)& ni(ii)& CO(ii)& L.分子对接研究证实了这些化合物与DNA的结合的强度和模式。所有复合物通过羟基机制有效地切断PUC18-DNA,通过将超硅形式转化为直链形式,Cu(II)复合物完全降解了DNA。该配合物证明了针对两种人类癌细胞系(MCF-7和A-549)的体外细胞毒性活性的可比性细胞毒性活性,其与顺铂相比。 AO / EB和DAPI染色研究表明,在这些癌细胞中,在调查中,这些癌细胞死亡的细胞死亡的凋亡模式。

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