Synthesis of [Ru(phen)2dppz]2+-tethered oligo-DNA and studies on the metallointercalation mode into the DNA duplex

被引:54
|
作者
Ossipov, D [1 ]
Pradeepkumar, PI [1 ]
Holmer, M [1 ]
Chattopadhyaya, J [1 ]
机构
[1] Univ Uppsala, Dept Bioorgan Chem, Biomed Ctr, Uppsala, Sweden
关键词
D O I
10.1021/ja003985t
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
To explore the binding properties of [Ru(phen)(2)dppz](2+) complex (phen = l,10-phenanthroline, dppz = dipyrido[3,2-a:2',3'-c]phenazine) in a sequence-specific manner in DNA duplex. it was tethered through the dppz ligand to a central position as well as both at the 3'- and 5'-ends of oligodeoxyribonucleotide (ODN). The middle [Ru(phen)(2)dppz](2+)-ODN tethered was resolved and isolated as four pure diastereomers, while the 3'- or 5'-[Ru(phen)(2)dppz](2+)-ODNs were inseparable on RP-HPLC. Thermal stability of the (Ru2+-ODN)- DNA duplexes is found to increase considerably (DeltaT(m) = 12.8-23.4 degreesC), depending upon the site of the covalent attachment of the tethered [Ru(phen)(2)dppz](2+) complex, or the chirality of the [Ru(phen)(2)dppz](2+)- linker tethered at the middle of the ODN, compared to the unlabeled counterpart. Gross differences in CD between the [Ru(phen)(2)dppz](2+)-tethered and the native DNA duplexes showed that the global duplex conformation of the former has considerably altered from the B-type, but is still recognized by DNase I. The thermal melting studies, CD measurements, as well as DNase I digestion data, are interpreted as a result of intercalation of the dppz moiety, which is realized by threading of the Ru(phen)(2) complex part through the DNA duplex core. DNase I footprinting with four diastereomerically pure middle ([Ru(phen)(2)dppz](2+)-ODN) DNA duplexes furthermore showed that the tethered [Ru(phen)(2)dppz](2+)-linker chirality dictates the stereo-chemical accessibility of various phosphodiester moieties (around the intercalation site) toward the cleavage reaction by the enzyme. The diastereomerically pure ruthenium-modified duplexes, with the well-defined pi -stack, will be useful to explore stereochemistry-dependent energy- and electron-transfer chemistry to understand oxidative damage to the DNA double helix as well as the long-range energy- and electron-transfer processes with DNA as a reactant.
引用
收藏
页码:3551 / 3562
页数:12
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