Photoactive RuII-Polypyridyl Complexes that Display Sequence Selectivity and High-Affinity Binding to Duplex DNA through Groove Binding

被引:58
|
作者
Ghosh, Amrita [2 ]
Das, Priyadip [2 ]
Gill, Martin R. [1 ]
Kar, Prasenjit [2 ]
Walker, Michaell G. [1 ]
Thomas, Jim A. [1 ]
Das, Amitava [2 ]
机构
[1] Univ Sheffield, Dept Chem, Sheffield S3 7HF, S Yorkshire, England
[2] Cent Salt & Marine Chem Res Inst, CSIR, Bhavnagar 364002, Gujarat, India
基金
英国工程与自然科学研究理事会;
关键词
DNA; groove binding; luminescence; molecular recognition; ruthenium; DINUCLEAR RUTHENIUM(II) COMPLEX; MIXED-LIGAND COMPLEXES; ELECTRON-TRANSFER; LIGHT-SWITCH; MINOR-GROOVE; CRYSTAL-STRUCTURE; NUCLEIC-ACIDS; METAL-COMPLEXES; EXCITED-STATE; X-RAY;
D O I
10.1002/chem.201002149
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The duplex-DNA binding properties of a nonintercalating polypyridyl ruthenium(II) complex that incorporates a linear extended ligand with a catechol moiety has been probed with a variety of photo- and biophysical techniques. These studies reveal that the complex groove binds to DNA sequences biphasically, and displays binding constants equivalent to those of high-affinity metallointercalators. The complex also displays preferential binding to AT-rich sequences. Changes in the structure of the coordinated catechol ligand and the incorporation of intercalating ancillary ligands into the complex were found to modulate both the optical-binding response and binding parameters of the system, which indicates that the catechol moiety plays a crucial role in the observed enhancement to binding affinities.
引用
收藏
页码:2089 / 2098
页数:10
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