Wood A A, Nunn C M, Czarny A, Boykin D W, Neidle S
CRC Biomolecular Structure Unit, Institute of Cancer Research, Surrey, UK.
Nucleic Acids Res. 1995 Sep 25;23(18):3678-84. doi: 10.1093/nar/23.18.3678.
An analogue of the DNA-binding compound Hoechst 33258, in which the piperazine ring has been replaced by an imidazoline group, has been cocrystallized with the dodecanucleotide sequence d(CGCGAATTCGCG)2. The structure has been solved by X-ray diffraction analysis and has been refined to an R-factor of 19.7% at a resolution of 2.0 A. The ligand is found to bind in the minor groove, at the central four AATT base pairs of the B-DNA double helix, with the involvement of a number of van der Waals contacts and hydrogen bonds. There are significant differences in minor groove width for the two compounds, along much of the AATT region. In particular this structure shows a narrower groove at the 3' end of the binding site consistent with the narrower cross-section of the imidazole group compared with the piperazine ring of Hoechst 33258 and therefore a smaller perturbation in groove width. The higher binding affinity to DNA shown by this analogue compared with Hoechst 33258 itself, has been rationalised in terms of these differences.
一种DNA结合化合物Hoechst 33258的类似物,其中哌嗪环已被咪唑啉基团取代,它已与十二聚核苷酸序列d(CGCGAATTCGCG)₂共结晶。该结构已通过X射线衍射分析解析出来,并在2.0 Å的分辨率下精修至R因子为19.7%。发现该配体结合在B-DNA双螺旋中央四个AATT碱基对处的小沟中,涉及许多范德华接触和氢键。在AATT区域的大部分范围内,这两种化合物的小沟宽度存在显著差异。特别是该结构在结合位点的3'端显示出较窄的沟,这与咪唑基团相比Hoechst 33258的哌嗪环具有更窄的横截面一致,因此对沟宽度的扰动较小。根据这些差异,已对该类似物与Hoechst 33258本身相比对DNA具有更高结合亲和力的现象作出了解释。