Levy A, Manoharan P T, Rifkind J M, Walker J C, Haberle F C, Kumar N G, Glickson J D, Elgavish G A
Laboratory of Cellular and Molecular Biology, NIA/NIH, Baltimore, MD 21224.
Biochim Biophys Acta. 1989 Apr 25;991(1):97-108. doi: 10.1016/0304-4165(89)90034-2.
Iron-57 Mössbauer, electron paramagnetic resonance (EPR) and H-1 nuclear magnetic resonance (NMR) studies of iron-bleomycin complexes in the pH range from 1.0 to 6.0 are reported. Sequential protonation of the ligands produces a variety of high-spin and low-spin complexes of the metal. Of particular interest is the reversible equilibrium between Fe(III)- and oxygen-stable Fe(II)-bleomycin. Below pH 3.5 Fe(II) complexes form, with maximal reduction occurring at approximately pH 2. At still lower pH, Fe(III) complexes unassociated with bleomycin become dominant. The observed reduction in the absence of exogenous reducing agents suggests the possible involvement of intramolecular autoreduction in bleomycin-mediated DNA degradation.
报道了在pH值为1.0至6.0范围内对铁-博来霉素复合物进行的铁-57穆斯堡尔、电子顺磁共振(EPR)和氢-1核磁共振(NMR)研究。配体的连续质子化产生了多种金属的高自旋和低自旋复合物。特别令人感兴趣的是Fe(III)-和氧稳定的Fe(II)-博来霉素之间的可逆平衡。在pH 3.5以下形成Fe(II)复合物,最大还原发生在约pH 2处。在更低的pH值下,与博来霉素无关的Fe(III)复合物占主导地位。在没有外源性还原剂的情况下观察到的还原表明分子内自动还原可能参与博来霉素介导的DNA降解。