首页> 外文期刊>Journal of biological inorganic chemistry: JBIC: a publication of the Society of Biological Inorganic Chemistry >Guanidine- and purine-functionalized ligands of (FeZnII)-Zn-III complexes: effects on the hydrolysis of DNA
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Guanidine- and purine-functionalized ligands of (FeZnII)-Zn-III complexes: effects on the hydrolysis of DNA

机译:(Feznii)-ZN-III复合物的胍和嘌呤官能化配体:对DNA水解的影响

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摘要

In this paper, the catalytic effects of aminoguanidine and aminopurine groups in the second sphere of a (FeZnII)-Zn-III complex that mimics the active site of the metallohydrolase purple acid phosphatase (PAP) are investigated, with a particular view on DNA as substrate. The ligand 3-(((3-((bis(2-(pyridin-2-yl)ethyl)amino)methyl)-2-hydroxy-5-methylbenzyl)(pyridin-2-ylmethyl)amino)meth-yl)-2 hydroxy-5-methylbenzaldehyde-(H(2)L(1)bpea) was synthesized and its complex [(OH)Fe-III(mu-OH)Zn-II(H2O)(L(1)bpea)](ClO4) was used as a base for comparison with similar complexes previously published in the literature. Subsequent modifications were conducted in the aldehyde group, where aminoguanidine (amig) and aminopurine (apur) were used as side chain derivatives. The complexes [(OH)Fe-III(mu-OH)Zn-II(H2O)(L(1)bpea)](ClO4) (1), [(OH)Fe-III(mu-OH)Zn-II(H2O)(L(1)bpea-amig)](ClO4) (2) and [(OH)Fe-III(mu-OH)Zn-II(H2O)(L(1)bpea-apur)](ClO4) (3) were characterized by spectroscopic methods (infrared, UV-Vis) and ESI-MS spectrometry. Density functional theory (DFT) was also used to better understand the structure of the complexes. The hydrolytic activity of complexes 1, 2 and 3 was analyzed using both the model substrate 2,4-BDNPP (bis-(2,4-dinitrophenyl)phosphate) and DNA. Complexes 2 and 3, containing the derivatized ligands, have a significantly higher association constant (K-assoc approximately equal to 1/K-M) for the activated substrate 2,4-BDNPP compared to complex 1. The catalytic efficiency (k(cat)/K-M) is also higher due to hydrogen bonds and/or pi-stacking interactions between the substrate and the aminoguanidine or aminopurine groups present in 2 and 3, respectively. In the DNA cleavage assays, all complexes were able to cleave DNA, with 1 and 2 having higher catalytic activity than 3. In addition, when compared to previously analyzed complexes, complex 2 is one of the most active, having a k(cat) of 0.21 h(-1).
机译:在本文中,研究了模拟金属水解酶紫酸性磷酸酶(PAP)的活性位点的(FeznII)-Zn-III复合物中的氨基胍和氨基嘌呤基团的催化作用,并对DNA进行了特定的观点基质。配体3 - (((3 - ((2-(2-)乙基)氨基)甲基)-2-羟基-5-甲基苄基)(吡啶-2-基甲基)氨基)甲基) -2羟基-5-甲基苯甲醛 - (H(2)L(1)BPEA)合成,其复合物[(OH)Fe-III(MU-OH)Zn-II(H 2 O)(L(1)BPEA)] (CLO4)用作与先前在文献中公布的类似复合物进行比较的基础。随后在醛基中进行后续修饰,其中氨基胍(Amig)和氨基嘌呤(Apur)用作侧链衍生物。复合物[(OH)Fe-III(MU-OH)Zn-II(H 2 O)(L(1)BPEA)](CLO 4)(1),[(OH)Fe-III(MU-OH)Zn-II (H 2 O)(L(1)BPEA-AMIG)](CLO 4)(2)和[(OH)Fe-III(MU-OH)Zn-II(H 2 O)(L(1)BPEA-APUR)](CLO4 )(3)以光谱方法(红外,UV-Vis)和ESI-MS光谱法为特征。密度泛函理论(DFT)也用于更好地理解复合物的结构。使用模型底物2,4-BDNPP(双 - (2,4-二硝基苯)磷酸酯)和DNA分析络合物1,2和3的水解活性。含有衍生化配体的配合物2和3具有与复合物1的活化底物2,4-BDNPP具有显着更高的恒定常数(k-assoc〜1 / km),与复合物1.催化效率(k(猫)/由于分别在2和3中存在的基材和氨基胍或氨基嘌呤基团之间的氢键和/或Pi堆叠相互作用,分别也较高。在DNA裂解测定中,所有复合物都能够裂开DNA,其中1和2具有较高的催化活性而不是3.另外,与先前分析的配合物相比,复合物2是最活跃的,具有AK(猫)之一0.21小时(-1)。

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