Kashanian S, Gholivand M B, Ahmadi F, Taravati A, Colagar A Hosseinzadeh
Department of Chemistry, Faculty of Science, Razi University, Kermanshah, Iran.
Spectrochim Acta A Mol Biomol Spectrosc. 2007 Jun;67(2):472-8. doi: 10.1016/j.saa.2006.08.017. Epub 2006 Aug 22.
The Al(III) complex, [Al(salophen)2H2O]NO3, was synthesized and characterized by spectroscopic (NMR and FT-IR) techniques. Then the binding of Schiff base complex of [Al(salophen)]+ type, where salophen denotes N,N'-bis(salicylidene) 2,2-phenylendiamine to calf thymus DNA, has been investigated by spectrophotometric, circular dichroism, spectrofluorometric, melting temperature and viscosimetric techniques. This Al(III) complex showed absorption hyperchromism in the range of 310-390 nm, increase in melting temperature, some structural changes in specific viscosity, when bound to calf thymus DNA. The binding constant has been determined using absorption measurement and found to be 1.82 x 10(3)M(-1) and 1.31 x 10(3)M(-1) in HEPES and Tris-HCl buffers, respectively. Also the fluorescence spectral characteristics and interaction of Al-salophen complex with DNA have been studied. Al-salophen bound to DNA showed a marked increase in the fluorescence intensity along with a bathochromic shift (5 nm). The intersection point of the binding isotherm indicated a binding site size of 12 bp per bound complex molecule in both HEPES and Tris-HCl buffers. The experimental results showed that the Al-salophen complex bound to DNA by non-intercalative mode and major groove binding was the preferred mode of interaction.
合成了铝(III)配合物[Al(salophen)₂H₂O]NO₃,并通过光谱(核磁共振和傅里叶变换红外光谱)技术对其进行了表征。然后,采用分光光度法、圆二色性、荧光光谱法、熔点温度法和粘度测定法研究了[Al(salophen)]⁺型席夫碱配合物(其中salophen表示N,N'-双(水杨醛)-2,2-苯二胺)与小牛胸腺DNA的结合情况。当该铝(III)配合物与小牛胸腺DNA结合时,在310 - 390 nm范围内表现出吸收增色效应,熔点温度升高,比粘度发生一些结构变化。通过吸收测量确定了结合常数,在HEPES和Tris - HCl缓冲液中分别为1.82×10³ M⁻¹和1.31×10³ M⁻¹。还研究了铝-水杨醛配合物与DNA的荧光光谱特性及相互作用。与DNA结合的铝-水杨醛配合物荧光强度显著增加,同时伴有红移(5 nm)。结合等温线的交点表明,在HEPES和Tris - HCl缓冲液中,每个结合的配合物分子的结合位点大小为12个碱基对。实验结果表明,铝-水杨醛配合物以非插入模式与DNA结合,且主要沟结合是优先的相互作用模式。