Instituto de Química, Universidade Federal Fluminense, Outeiro S. João Batista S/N, Niterói, RJ, 24020-141, Brazil.
nanoBIC, Departament de Química Inorgànica i Orgànica, Secció Química Inorgànica, Universitat de Barcelona, Martí i Franquès 1-11, 08028, Barcelona, Spain.
J Biol Inorg Chem. 2021 Sep;26(6):727-740. doi: 10.1007/s00775-021-01888-2. Epub 2021 Aug 28.
Two square-planar coordination compounds, namely [Cu(CPYA)Cl] (1) and [Pd(CPYA)Cl] (2), were prepared from the ligand 4-chloro-N-(pyridin-2-ylmethyl)aniline (CPYA) and two chloride salts, and were fully characterized, including by X-ray diffraction. Spectroscopic, electrophoretic and AFM studies revealed that the two isostructural compounds were interacting differently with DNA. In both cases, the initial interaction involves electrostatic contacts of the CPYA ligand in the minor groove (as suggested by molecular docking), but subsequent strong binding occurs with the palladium(II) complex 2, whereas the binding with the copper complex 1 is weaker and concentration dependent. The strong binding of 2 eventually leads to the cleavage of the double strand and the redox activity of 1 allows to oxidatively cleave the biomolecule.
两个平面正方形配位化合物,即[Cu(CPYA)Cl](1)和[Pd(CPYA)Cl](2),是由配体 4-氯-N-(吡啶-2-基甲基)苯胺(CPYA)和两种氯化盐制备的,并通过 X 射线衍射进行了充分的表征。光谱、电泳和 AFM 研究表明,这两种同构化合物与 DNA 的相互作用方式不同。在这两种情况下,初始相互作用都涉及到 CPYA 配体在小沟中的静电相互作用(如分子对接所建议的),但随后会与钯(II)配合物 2 发生强烈的结合,而与铜配合物 1 的结合则较弱且与浓度有关。2 的强烈结合最终导致双链的断裂,而 1 的氧化还原活性允许氧化切割生物分子。