Minor-Groove Binding Drugs: Where Is the Second Hoechst 33258 Molecule?

被引:44
|
作者
Fornander, Louise H. [1 ]
Wu, Lisha [1 ]
Billeter, Martin [2 ]
Lincoln, Per [1 ]
Norden, Bengt [1 ]
机构
[1] Chalmers Univ Technol, Dept Chem & Biol Engn, S-41296 Gothenburg, Sweden
[2] Univ Gothenburg, Dept Chem & Mol Biol, SE-40530 Gothenburg, Sweden
基金
欧洲研究理事会;
关键词
CIRCULAR-DICHROISM; DNA; RECOGNITION; 4,6-DIAMIDINO-2-PHENYLINDOLE; COMPLEXES; LIGANDS; SPECIFICITY; ASSOCIATION; NETROPSIN; PROTEIN;
D O I
10.1021/jp400418w
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Hoechst 33258 binds with high affinity into the minor groove of AT-rich sequences of double-helical DNA. Despite extensive studies of this and analogous DNA binding molecules, there still remains uncertainty concerning the interactions when multiple ligand molecules are accommodated within close distance. Albeit not of direct concern for most biomedical applications, which are at low drug concentrations, interaction studies for higher drug binding are important as they can give fundamental insight into binding mechanisms and specificity, including drug self-stacking interactions that can provide base-sequence specificity. Using circular dichroism (CD), isothermal titration calorimetry (ITC), and proton nuclear magnetic resonance CH NMR), we examine the binding of Hoechst 33258 to three oligonucleotide duplexes containing AT regions of different lengths: [d(CGCGAATTCGCG)](2) (A(2)T(2)), [d(CGCAAATTTGCG)](2) (A(3)T(3)), and [d(CGAAAATTTTCG)](2) (A(4)T(4)). We find similar binding geometries in the minor groove for all oligonucleotides when the ligand-to-duplex ratio is less than 1:1. At higher ratios, a second ligand can be accommodated in the minor groove of A(4)T(4) but not A(2)T(2) or A(3)T(3). We conclude that the binding of the second Hoechst to A(4)T(4) is not cooperative and that the molecules are sitting with a small separation apart, one after the other, and not in a sandwich structure as previously proposed.
引用
收藏
页码:5820 / 5830
页数:11
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