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以壳寡糖与对羟基苯甲醛反应合成的席夫碱化合物作为配体,构建了一系列的金属Cu(Ⅱ)配合物,并通过紫外光谱法、电化学手段以及粘度实验,初步研究了配合物与DNA的作用机理。紫外光谱实验发现,配合物的特征吸收峰在加入DNA后峰位均呈现红移和减色;从循环伏安曲线可见,DNA加入后配合物的氧化峰电流呈下降趋势,峰电位伴随有正移趋势;DNA的粘度随着配合物浓度的依次增大,呈先增大后降低的趋势。结合以上这些信息,认为配合物与DNA以部分嵌插方式作用的。 相似文献
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合成了2种三齿多吡啶钴(Ⅱ)配合物,用元素分析、IR等对它们进行了表征,用循环伏安法、电子吸收光谱、荧光光谱等方法研究了配合物与CT DNA的相互作用以及配合物对pBR322DNA的断裂作用.结果表明,配合物[Co(PhTPY)2]2+与DNA的作用属中等强度的部分插入,配合物[Co(H2 Bzimpy)2]2+与DNA的作用属静电作用.凝胶电泳实验表明,用310 nm光辐射15 min,配合物[Co(PhTPY)2]2+可选择性地断裂pBR322DNA为开环缺口性和线型DNA,配合物[Co(H2 Bzimpy)2]2+对DNA的断裂没有选择性. 相似文献
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合成了一种三齿配体N-(4-甲基苯)-N′-(2-(4-甲基苯氨基)乙基)乙烷-1,2-二胺,并制备了它的3种过渡金属配合物[ML(H2O)2Cl]Cl(M=CuⅡ,CoⅡ,NiⅡ),用元素分析、核磁、红外和摩尔电导等表征了配体及其金属配合物的组成和结构。对Ni—L进行了单晶结构解析,配合物为六配位的八面体结构,配体采用三齿配位。利用紫外光谱和荧光光谱法研究了配合物与小牛胸腺DNA的作用方式,结果表明,3种金属配合物可能以静电方式与DNA作用。Cu—L、Ni—L、Co—L3种配合物与DNA的结合常数分别为2.99×104、9.78×103、3.66×103。 相似文献
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以1,10-菲罗啉、壳聚糖和四水合乙酸钴为原料,合成了水溶性壳聚糖钴(II)配合物(CHT-Co(II)),采用红外光谱对配体及配合物进行了表征。在pH 7.5的Tris-HCl缓冲溶液中,采用粘度法、紫外可见吸收光谱法和电化学方法(循环伏安法,微分脉冲伏安法)研究了配合物与DNA的相互作用。粘度法表明二者能发生部分嵌插作用;DNA的加入能引起配合物紫外光谱的变化也表明了二者之间的相互作用。电化学实验表明配合物在玻碳电极上的氧化还原为一可逆过程,当加入一定量的DNA时,配合物的氧化峰电流明显降低,式电位有所正移,验证了二者之间存在部分嵌插作用。 相似文献
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《化学试剂》2015,(12)
合成了一种多吡啶铜(Ⅱ)配合物,用红外光谱、元素分析、X-射线单晶衍射法对配合物的组成和结构进行了表征。该配合物的晶体属单斜晶系,P2(1)/c空间群。用荧光光谱、紫外光谱研究了配合物与小牛胸腺DNA的键合作用。结果表明,配合物与DNA的键合作用属部分插入,结合常数K_b=8.0×104L/mol。用凝胶电泳法研究了配合物对p BR322DNA的切割作用。实验表明,配合物用310 nm光辐射15 min,可将p BR322 DNA断裂为开口缺刻型和线型DNA。采用MTT法研究了配合物对人乳腺癌细胞和肺癌细胞的体外抗肿瘤活性。结果发现,所合成配合物能有效抑制这两种细胞增殖。 相似文献
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Kamila Stokowa-Sotys Kamil Wojtkowiak Valentyn Dzyhovskyi Robert Wieczorek 《International journal of molecular sciences》2021,22(22)
Fusobacterium nucleatum is one of the most notorious species involved in colorectal cancer. It was reported that numerous outer membrane proteins (OMP) are actively involved in carcinogenesis. In this paper, the structure and stability of certain complexes, as well as DNA cleavage and ROS generation by fragments of OMP, were investigated using experimental and theoretical methods. Mass spectrometry, potentiometry, UV-Vis, CD, EPR, gel electrophoresis and calculations at the density functional theory (DFT) level were applied. Two consecutive model peptides, Ac-AKGHEHQLE-NH2 and Ac-FGEHEHGRD-NH2, were studied. Both of these were rendered to form a variety of thermodynamically stable complexes with copper(II) ions. All of the complexes were stabilized, mainly due to interactions of metal with nitrogen and oxygen donor atoms, as well as rich hydrogen bond networks. It was also concluded that these complexes in the presence of hydrogen peroxide or ascorbic acid can effectively produce hydroxyl radicals and have an ability to cleave the DNA strands. Surprisingly, the second studied ligand at the micromolar concentration range causes overall DNA degradation. 相似文献
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Yong Li Zheng-Yin Yang Zhen-Chuan Liao Zi-Chao Han Zeng-Chen Liu 《Inorganic chemistry communications》2010,13(10):1213-1216
3-Carbaldehyde-chromone semicarbazone (L) and its Cu(II), Zn(II), Ni(II) complexes were synthesized and characterized on the basis of crystal structure and other structural characterization methods. The metal ions and Schiff base ligand can form mononuclear five-coordination complexes with 1:1 metal-to-ligand stoichiometry at the metal ions as centres. The transition metal complexes may be used as potential anticancer drugs, because they bind to calf thymus DNA via an intercalation binding mode with the binding constants at the order of magnitude 105–106 M? 1, and the metal complexes present stronger DNA binding affinities than the free ligand alone. In addition, the antioxidant activities of the ligand and its metal complexes were investigated through scavenging effects for superoxide anion and hydroxyl radical in vitro, indicating that the compounds show stronger antioxidant activities than some standard antioxidants, such as mannitol and vitamin C. 相似文献
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Impact of metallonucleases on DNA interactions: Structural validation and in-vitro antibiogram assay
Four novel complexes were synthesized using 2-aminobenzophenone Schiff base precursor and characterized by various analytical techniques. FT-IR results demonstrate that the Schiff base ligand, obtained by the condensation of 2-aminobenzophenone with 2-hydroxybenzaldehyde, coordinates to the metal ion via azomethine nitrogen, phenolic oxygen and carbonyl groups. Furthermore, the intercalative mode of these octahedral complexes with calf thymus (CT) DNA has been explored using absorption spectra, cyclic voltammetric and viscosity measurements. Gel electrophoresis assay demonstrates the effective cleaving aptitude of pBR322 DNA by complexes in the presence of an activating agent (H2O2). Moreover, the in-vitro biological activities of metal complexes have been screened against few pathogenic bacterial and fungal strains by well diffusion technique. It is found that all the complexes show potential activities as compared to the free ligand. These findings may lead to develop novel DNA targeting metallonucleases. 相似文献
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Dr. Nicolò Zuin Fantoni Prof. Dr. Tom Brown Prof. Dr. Andrew Kellett 《Chembiochem : a European journal of chemical biology》2021,22(13):2184-2205
DNA binding metal complexes are synonymous with anticancer drug discovery. Given the array of structural and chemical reactivity properties available through careful design, metal complexes have been directed to bind nucleic acid structures through covalent or noncovalent binding modes. Several recognition modes – including crosslinking, intercalation, and oxidation – are central to the clinical success of broad-spectrum anticancer metallodrugs. However, recent progress in nucleic acid click chemistry coupled with advancement in our understanding of metal complex–nucleic acid interactions has opened up new avenues in genetic engineering and targeted therapies. Several of these applications are enabled by the hybridisation of oligonucleotide or polyamine probes to discrete metal complexes, which facilitate site-specific reactivity at the nucleic acid interface under the guidance of the probe. This Review focuses on recent advancements in hybrid design and, by way of an introduction to this topic, we provide a detailed overview of nucleic acid structures and metal complex–nucleic acid interactions. Our aim is to provide readers with an insight on the rational design of metal complexes with DNA recognition properties and an understanding of how the sequence-specific targeting of these interactions can be achieved for gene engineering applications. 相似文献
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文章对过渡金属配合物与DNA相互作用的研究和应用进行了归纳和分析,在过渡金属配合物可用于DNA分子光开关、DNA二级结构探针、DNA错配碱基识别探针、DNA切割试剂等方面进行了总结和探索。 相似文献
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The modes and activities of the interaction of DNA and water‐soluble polymeric Schiff base–nickel complexes, which have been prepared by polymeric analogous reaction, have been discussed according to absorption spectra, circular dichroism spectra, and fluorescent probe method. It is indicated that polymeric matrix effect and increasing solubility in water can increase the interaction of these water‐soluble polymeric metal complexes with DNA. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 84: 887–893, 2002; DOI 10.1002/app.10000 相似文献
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自从发现顺铂具有抗癌活性以来,金属配合物作为新一类抗癌药物引起了人们的广泛关注。综述了近年来铂类配合物、钌类配合物和席夫碱配合物在抗癌药物中的研究进展,重点阐述了铂类配合物抗癌活性的研究现状及作用原理,并对金属配合物抗癌活性的研究进展进行总结,为金属配合物抗癌药物研究提供参考和依据。 相似文献