Teng M K, Usman N, Frederick C A, Wang A H
Department of Biology, Massachusetts Institute of Technology, Cambridge 02139.
Nucleic Acids Res. 1988 Mar 25;16(6):2671-90. doi: 10.1093/nar/16.6.2671.
The crystal structure of the complex between the dodecamer d(CGCGAATTCGCG) and a synthetic dye molecule Hoechst 33258 was solved by X-ray diffraction analysis and refined to an R-factor of 15.7% at 2.25 A resolution. The crescent-shaped Hoechst compound is found to bind to the central four AATT base pairs in the narrow minor groove of the B-DNA double helix. The piperazine ring of the drug has its flat face almost parallel to the aromatic bisbenzimidazole ring and lies sideways in the minor groove. No evidence of disordered structure of the drug is seen in the complex. The binding of Hoechst to DNA is stabilized by a combination of hydrogen bonding, van der Waals interaction and electrostatic interactions. The binding preference for AT base pairs by the drug is the result of the close contact between the Hoechst molecule and the C2 hydrogen atoms of adenine. The nature of these contacts precludes the binding of the drug to G-C base pairs due to the presence of N2 amino groups of guanines. The present crystal structural information agrees well with the data obtained from chemical footprinting experiments.
通过X射线衍射分析解析了十二聚体d(CGCGAATTCGCG)与合成染料分子Hoechst 33258之间复合物的晶体结构,并在2.25 Å分辨率下精修至R因子为15.7%。发现新月形的Hoechst化合物结合于B-DNA双螺旋窄小沟中的中央四个AATT碱基对。药物的哌嗪环其平面几乎与芳香族双苯并咪唑环平行,并侧卧于小沟中。在复合物中未观察到药物无序结构的迹象。Hoechst与DNA的结合通过氢键、范德华相互作用和静电相互作用的组合得以稳定。药物对AT碱基对的结合偏好是Hoechst分子与腺嘌呤的C2氢原子紧密接触的结果。由于鸟嘌呤存在N2氨基,这些接触的性质排除了药物与G-C碱基对的结合。目前的晶体结构信息与化学足迹实验获得的数据非常吻合。