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Binding of piano-stool Ru(II) complexes to DNA; QM/MM study

Publikace na Matematicko-fyzikální fakulta |
2012

Tento text není v aktuálním jazyce dostupný. Zobrazuje se verze "en".Abstrakt

Ru(II) piano-stool complexes belong to group of biologically active metallocomplexes with promising anticancer activity. In this study, we investigate the reaction mechanism of [(eta 6-benzene)Ru(II)(en)(H2O)]2+ (en = ethylenediamine) complex binding to DNA by hybrid QM/MM computational techniques.

The reaction when the Ru(II) complex is coordinated on N7-guanine from major groove is explored. Two reaction pathways, direct binding to N7 position and two-step mechanism passing through O6 position, are considered.

It was found that the reaction is exothermic and the direct binding process is preferred kinetically. In analogy to cisplatin, we also explored the possibility of intrastrand cross-link formation where the Ru(II) complex makes a bridge between two adjacent guanines.

Two different pathways were found, leading to a final structure with released benzene ligand. This process is exothermic; however, one pathway is blocked by relatively high initial activation barrier.

Geometries, energies, and electronic properties analyzed by atoms in molecules and natural population analysis methods are discussed. (c) 2012 Wiley Periodicals, Inc.