Sultan Kincal, Tolga Göktürk, Cansu Topkaya, Ramazan Güp
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摘要

近年来,设计和合成具有生物学、结构和配位性质的人工核酸酶的研究越来越多。本研究用Cu(II)、Ni(II)和Zn(II)过渡金属离子盐的双酰基腙配体获得了具有潜在生物活性的单核配合物,其结构中有N和O等旋转原子。利用FTIR、uv -可见、1H-NMR、TGA、元素分析和磁化率等技术对所得到的配合物的特征结构进行了表征。利用紫外可见吸收滴定法研究了潜在的人工金属核酸酶的dna结合活性,并对其结构进行了分析。此外,用琼脂糖凝胶电泳法分析了它们的dna裂解活性。作为本研究的一部分,确定了DNA的结合模式和切割机制。根据得到的结果,确定了DNA与复合物之间的结合模式是非共价相互作用。已经证明,这些化合物可以氧化和水解裂解DNA。研究表明,参与DNA裂解活性的自由基有H2O2、超氧自由基和羟基自由基。结果表明,Cu(II)配合物具有最高的解理和键合作用,其次是Ni(II)和Zn(II)配合物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
ÜÇ YENİ BİS(AÇİLHİDRAZON) MONONÜKLEER GEÇIŞ METALI KOMPLEKSİ: SENTEZ, KARAKTERİZASYON VE DNA ETKİLEŞİM ÇALIŞMALARI
In recent years, studies on the design and synthesis of artificial nucleases with biological, structural and coordination properties have been increasing. With this study, mononuclear complex compounds were obtained with Cu(II), Ni(II) and Zn(II) transition metal ion salts of bis(acylhydrazone) ligand, which has the potential to show biological activity and has revolving atoms such as N and O in its structure. The characteristic structures of the obtained complex compounds were elucidated using various techniques such as FTIR, UV-Visible, 1H-NMR, TGA, elemental analysis and magnetic susceptibility. The DNA-binding activities of potential artificial metallonucleases, whose structures were elucidated, were investigated using the UV-visible absorption titration method. Additionally, their DNA-cleavge activities were analyzed using the agarose gel electrophoresis method. The DNA binding mode and cleavage mechanisms were determined as part of this study.. In line with the results obtained, it was determined that the binding mode between DNA and the complexes is a noncovalent interaction. It has been demonstrated that the compounds cleavage DNA both oxidatively and hydrolytically. It has been revealed that the radicals involved in DNA cleavage activity are H2O2, superoxide and hydroxyl radicals. It was revealed that the compound with the highest cleavage and bonding interaction was the Cu(II) complex, followed by Ni(II) and Zn(II) complexes.
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