Parkinson J A, Barber J, Douglas K T, Rosamond J, Sharples D
Department of Pharmacy, University of Manchester, U.K.
Biochemistry. 1990 Nov 6;29(44):10181-90. doi: 10.1021/bi00496a005.
The interaction of Hoechst 33258, a fluorescent DNA stain, has been studied by using the synthetic, self-complementary oligonucleotide duplex d(CGCGAATTCGCG)2. Spectrofluorometric Scatchard analysis indicated that there was only a single class of binding site and that the 1:1 complex had a dissociation constant of (3.47 +/- 0.1) X 10(-6) M at 25 degrees C. Spectroscopic titration by high-field 1H NMR confirmed the 1:1 complex and by means of ID and 2D (NOESY, COSY) techniques the binding site was defined as the minor groove formed by the AATT stretch. Plentiful cross-peaks were measurable and resonance doubling occurred because of the lifting of the diad symmetry of the oligonucleotide on ligand binding. Many individual resonances of both strands of the DNA could be assigned for the complex because of these features, along with the occurrence of slow exchange on the NMR time scale. The results of this NMR spectroscopic solution study were compared with those of previous X-ray crystallographic studies of the same complex. From nuclear Overhauser effect data measured for the complex, a detailed three-dimensional model was constructed with the aid of molecular graphics.
通过使用合成的、自我互补的寡核苷酸双链体d(CGCGAATTCGCG)₂,对荧光DNA染料Hoechst 33258的相互作用进行了研究。荧光分光光度法的Scatchard分析表明,只有一类结合位点,且在25℃时1:1复合物的解离常数为(3.47±0.1)×10⁻⁶ M。通过高场¹H NMR进行的光谱滴定证实了1:1复合物,并借助一维和二维(NOESY、COSY)技术将结合位点定义为由AATT序列形成的小沟。由于配体结合时寡核苷酸的二重对称性被打破,可测量到大量的交叉峰且出现了共振加倍现象。由于这些特征以及在NMR时间尺度上的慢交换现象,DNA双链的许多单个共振峰都可被指定给该复合物。将该NMR光谱溶液研究的结果与先前对同一复合物的X射线晶体学研究结果进行了比较。根据对该复合物测量的核Overhauser效应数据,借助分子图形构建了一个详细的三维模型。