含lawsone配体的铕(III)和铽(III)配合物的合成、表征及其与DNA、HSA和拓扑异构酶的相互作用

IF 4.7 2区 化学 Q2 CHEMISTRY, PHYSICAL Journal of Molecular Structure Pub Date : 2025-06-25 Epub Date: 2025-02-18 DOI:10.1016/j.molstruc.2025.141790
Josias S. Rocha , George B.S. Pereira , Marcos V. Palmeira-Mello , Willyan F. Oliveira , Jocely L. Dutra , Tamara Teixeira , Nádija N.P. da Silva , Gabriela P. Oliveira , Paulo C. Gomes-Junior , Anna C.S.J. Passaes , João H. Araujo-Neto , Alzir A. Batista , Javier Ellena , José D.L. Dutra , Renan L. Farias , Fillipe V. Rocha
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引用次数: 0

摘要

本研究合成了铕[Eu(LAW)3(H2O)3](1)和铽[Tb(LAW)3(H2O)3](2)两种含有lawsone配体的配合物,并利用红外光谱和紫外可见光谱、循环伏安法、电导率和磁化率测量对其进行了综合表征。通过x射线衍射(XRD)测定了晶体结构信息,元素分析证实了化合物的纯度。通过TD-DFT计算比较了实验和理论的UV-Vis数据,为Eu(III)和Tb(III)配合物的低发光提供了见解,并计算了在有和没有溶剂作用下的激发态。利用粘度测量、紫外-可见滴定、圆二色性和荧光竞争分析等方法进行了ct-DNA的DNA结合实验,以探索复合物与DNA靶标的主要相互作用。此外,用琼脂糖凝胶电泳检测pBR322质粒DNA的切割特性。虽然没有观察到裂解活性,但DNA相互作用研究表明,黏度和圆二色性数据支持共价结合。此外,分析对接结果,这两种化合物在Sudlow I位点具有稳定的构象,并且基于lawson的化合物显示出与人血清白蛋白(HSA)结合的能力,结合常数(Kb)在105-106范围内,并且在50µM时表现出拓扑异构酶Iα抑制作用。这两种化合物在48小时内都保持稳定。
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Synthesis, characterization of europium(III) and terbium(III) complexes containing lawsone ligand and their interaction with DNA, HSA, and topoisomerases
In this study, two complexes based on Europium [Eu(LAW)3(H2O)3] (1) and Terbium [Tb(LAW)3(H2O)3] (2), each containing the lawsone ligand, were synthesized and comprehensively characterized using Infrared and UV-Visible spectroscopies, Cyclic Voltammetry, Conductivity, and Magnetic Susceptibility measurements. Crystal structure information was determined via X-ray diffraction (XRD), and elemental analysis confirmed the compounds’ purity. Experimental and theoretical UV-Vis data were compared through TD-DFT calculations, providing insights into the low luminescence of both Eu(III) and Tb(III) complexes, with excited states calculated both with and without solvent effects. DNA-binding experiments with ct-DNA were conducted using viscosity measurements, UV-Vis titrations, circular dichroism, and fluorescence competition assays to explore the complexes' primary interactions with the DNA target. Additionally, DNA cleavage properties were examined using pBR322 plasmid DNA with agarose gel electrophoresis. Although no cleavage activity was observed, DNA interaction studies suggested covalent binding, supported by viscosity and circular dichroism data. Furthermore, analyzing the docking results, both compounds demonstrated stable conformations within the Sudlow I site also the lawsone-based compounds demonstrated an ability to bind to human serum albumin (HSA) with binding constants (Kb) in the range of 105-106 and showed Topoisomerase IIα inhibition at 50 µM. Both compounds remained stable for up to 48 hours.
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来源期刊
Journal of Molecular Structure
Journal of Molecular Structure 化学-物理化学
CiteScore
7.10
自引率
15.80%
发文量
2384
审稿时长
45 days
期刊介绍: The Journal of Molecular Structure is dedicated to the publication of full-length articles and review papers, providing important new structural information on all types of chemical species including: • Stable and unstable molecules in all types of environments (vapour, molecular beam, liquid, solution, liquid crystal, solid state, matrix-isolated, surface-absorbed etc.) • Chemical intermediates • Molecules in excited states • Biological molecules • Polymers. The methods used may include any combination of spectroscopic and non-spectroscopic techniques, for example: • Infrared spectroscopy (mid, far, near) • Raman spectroscopy and non-linear Raman methods (CARS, etc.) • Electronic absorption spectroscopy • Optical rotatory dispersion and circular dichroism • Fluorescence and phosphorescence techniques • Electron spectroscopies (PES, XPS), EXAFS, etc. • Microwave spectroscopy • Electron diffraction • NMR and ESR spectroscopies • Mössbauer spectroscopy • X-ray crystallography • Charge Density Analyses • Computational Studies (supplementing experimental methods) We encourage publications combining theoretical and experimental approaches. The structural insights gained by the studies should be correlated with the properties, activity and/ or reactivity of the molecule under investigation and the relevance of this molecule and its implications should be discussed.
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