Kainosho M, Takahashi M
Nucleic Acids Symp Ser. 1983(12):181-4.
Structures of the equimolar uranyl complexes of various 5'-nucleotides, such as AMP, GMP, UMP, and CMP, were extensively studied by high-field proton NMR spectroscopy. The unambiguous assignment of the proton resonances was established by correlating with the C-13 NMR spectrum of the complex from [N-15]AMP, which showed a doublet for the C-1' carbon signal due to the spin coupling with N-15 (N-9). Uranyl-nucleotide complexes were found to be the mixture of several oligomeric species having a common structural unit. The primary coordination sites of the uranyl ion were phosphate and 3'-hydroxyl oxygens, but no interaction was observed for the bases. The major oligomer at a high pH (above 11) was a cage-like octamer, and two isomeric cyclic tetramers predominated at a lower pH (below 10).
通过高场质子核磁共振光谱对各种5'-核苷酸(如AMP、GMP、UMP和CMP)的等摩尔铀酰配合物的结构进行了广泛研究。通过与来自[N-15]AMP的配合物的C-13核磁共振光谱相关联,确定了质子共振的明确归属,该光谱显示由于与N-15(N-9)的自旋耦合,C-1'碳信号为双峰。发现铀酰-核苷酸配合物是具有共同结构单元的几种寡聚体物种的混合物。铀酰离子的主要配位点是磷酸根和3'-羟基氧,但未观察到与碱基的相互作用。在高pH值(高于11)下的主要寡聚体是笼状八聚体,在较低pH值(低于10)下两种异构环状四聚体占主导。