Department of Chemistry, University of Isfahan, Isfahan, Iran.
Spectrochim Acta A Mol Biomol Spectrosc. 2012 May;90:50-4. doi: 10.1016/j.saa.2012.01.015. Epub 2012 Jan 16.
The DNA binding properties of a bulky and hydrophobic Schiff base complex of manganese(III) [N,N'-bis(5-(triphenyl phosphonium methyl)salicylidene)-1,2-ethylene diamine chloride Mn(III) acetate] was examined by spectroscopic techniques. UV-vis titration data indicate both hypo and hyperchromic effect with addition of DNA to complex. A competitive binding study showed that the enhanced emission intensity of ethidium bromide (EB) in the presence of DNA was quenched by adding Mn Salen complex. This finding indicates that Mn Salen complex displaces EB from its binding site in DNA. Helix melting studies indicate improvement in the helix stability, and an increase in the melting temperature. The analysis of CD spectra represents the structural changes in DNA due to the binding of Mn Salen complex. The binding constant has been calculated using absorbance and fluorescence data. The results also represent that the binding process proceeds by strong electrostatic and hydrophobic interactions.
采用光谱技术研究了锰(III)[N,N'-双(5-(三苯基膦甲基)水杨醛亚胺)-1,2-乙二胺二氯化物乙酸锰(III)]的庞大且疏水席夫碱配合物的 DNA 结合性质。紫外可见滴定数据表明,随着 DNA 的加入,复合物具有低色和高色效应。竞争性结合研究表明,在 DNA 存在下,溴化乙锭(EB)的增强发射强度被添加的 Mn Salen 配合物猝灭。这一发现表明 Mn Salen 配合物将 EB 从其在 DNA 中的结合位点置换出来。螺旋熔融研究表明螺旋稳定性得到改善,熔融温度升高。CD 光谱分析代表了由于 Mn Salen 配合物的结合而导致的 DNA 结构变化。使用吸光度和荧光数据计算了结合常数。结果还表明,结合过程是通过强静电和疏水相互作用进行的。