Veselkov A N, Devis D, Dymant L N, Parkes Kh
Sevastopol Instrument-Development Institute, Birkbeck College, London University, UK.
Biofizika. 1992 Jan-Feb;37(1):23-33.
Complex formation between acridine dye proflavine and self-complementary deoxytetraribonucleoside triphosphate 5'-d(ApGpCpT) in water-salt solution was studied by the method of one- and two-dimensional 1H-NMR spectroscopy (500 MHz). Two-dimensional homonuclear 1H-NMR spectroscopy (2D-COSY and 2D-NOESY) was used for complete assignments of proton signals of molecules in solution and for qualitative analysis of the nature of interactions between proflavine and tetranucleotide. Concentration dependences of proton chemical shifts of the molecules were measured at 293 K. Equilibrium reaction constants and limiting chemical shifts of dye protons in the complexes were determined using suggested schemes of complex formation. Based on the obtained data possible types of complexes were considered. Analysis of relative content of different types of complexes was made and special features of dynamic equilibrium were revealed as a function of correlation of dye and tetranucleotide concentrations. The most favourable structure of 1:2 complex of dye with tetranucleotide was constructed using the calculated values of induced chemical shifts of proflavine protons and 2D-NOESY spectra.
采用一维和二维¹H-NMR光谱法(500 MHz)研究了吖啶染料硫酸原黄素与自互补脱氧四核糖核苷三磷酸5'-d(ApGpCpT)在水盐溶液中的络合物形成。二维同核¹H-NMR光谱(二维COSY和二维NOESY)用于溶液中分子质子信号的完全归属以及原黄素与四核苷酸之间相互作用性质的定性分析。在293 K下测量了分子质子化学位移的浓度依赖性。使用建议的络合物形成方案确定了络合物中染料质子的平衡反应常数和极限化学位移。基于获得的数据,考虑了可能的络合物类型。分析了不同类型络合物的相对含量,并揭示了作为染料和四核苷酸浓度相关性函数的动态平衡特征。利用原黄素质子的诱导化学位移计算值和二维NOESY光谱构建了染料与四核苷酸1:2络合物的最有利结构。