以芳香含氮杂环为桥接配体的双核金配合物的Dna / bsa结合研究

Tina P. Andrejević, Darko P Ašanin, Nada D. Savić, N. Stevanović, M. Djuran, Biljana Đ. Glišić
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摘要

近几十年来,由于金(III)配合物与铂(II)配合物的结构相似,人们特别关注金(III)配合物作为潜在的抗肿瘤药物。金(III)配合物抗肿瘤活性模式的可能机制之一可能包括它们与DNA的相互作用。然而,治疗剂的有效性还取决于其与血浆中存在的蛋白质的结合程度,因为通过这种方式,它被运送到细胞中。考虑到这一点,我们研究了三种双核金(III)配合物[{AuCl3}2(μ - L)], L = 4,4 ' -bipy(4,4 ' -联吡啶,Au1), bpe(1,2-二(4-吡啶基)乙烷,Au2)和dpe(1,2-二(4-吡啶基)乙烷,Au3)与小牛胸腺DNA (ct-DNA)和牛血清白蛋白(BSA)的相互作用。该研究的主要目的是评估金(III)配合物Au1-3对这些生物分子的结合亲和力,以可能了解其生物活性模式。Au1-3与ct-DNA的结合常数(KA)高于与BSA的结合常数,表明复合物对该核酸具有更大的亲和力。Au1的分配系数(logP)值高于其他两种配合物的相应值,这与该配合物的细胞摄取效率较高是一致的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
DNA/BSA BINDING STUDY OF DINUCLEAR GOLD(III) COMPLEXES WITH AROMATIC NITROGEN-CONTAINING HETEROCYCLES AS BRIDGING LIGANDS
In recent decades, a special attention has been devoted to gold(III) complexes as potential antitumor agents due to their structural similarity to platinum(II) complexes. One of the possible mechanisms of the mode of antitumor activity of gold(III) complexes could include their interaction with DNA. However, the effectiveness of the therapeutic agents also depends on the degree of its binding to proteins present in the blood plasma, because, in this way, it is transported to the cell. Considering this, we investigated the interactions of three dinuclear gold(III) complexes of the general formula [{AuCl3}2(μ– L)], L = 4,4’-bipy (4,4’-bipyridine, Au1), bpe (1,2-bis(4-pyridyl)ethane, Au2) and dpe (1,2-bis(4- pyridyl)ethene, Au3) with calf thymus DNA (ct-DNA) and bovine serum albumin (BSA). The main aim of the study was to evaluate the binding affinities of gold(III) complexes Au1–3 towards these biomolecules for possible insights on their mode of biological activity. The values of binding constants (KA) of Au1–3 to ct-DNA are higher than those for BSA, indicating greater affinity of the complexes towards this nucleic acid. The partition coefficient (logP) value for Au1 is higher compared to the corresponding values for the other two complexes, what is in accordance with a higher cellular uptake efficiency of this complex.
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