Insights into Intrastrand Cross-Link Lesions of DNA from QM/MM Molecular Dynamics Simulations

• Published in: Journal of the American Chemical Society Vol. 134; no. 4; pp. 2111 - 2119
• Main Authors: Garrec, Julian, Patel, Chandan, Rothlisberger, Ursula, Dumont, Elise
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 01.02.2012
• Subjects: Chemical Sciences; crosslinking; DNA; DNA - chemistry; DNA damage; Gibbs free energy; hydrogen bonding; Models, Molecular; molecular dynamics; Molecular Dynamics Simulation; or physical chemistry; pyrimidines; quantum mechanics; standard operating procedures; Theoretical and
• ISSN: 0002-7863; 1520-5126; 1520-5126
• DOI: 10.1021/ja2084042

DNA damages induced by oxidative intrastrand cross-links have been the subject of intense research during the past decade. Yet, the currently available experimental protocols used to isolate such lesions only allow to get structural information about linked dinucleotides. The detailed structure of the damaged DNA macromolecule has remained elusive. In this study we generated in silico the most frequent oxidative intrastrand cross-link adduct, G­[8,5-Me]­T, embedded in a solvated DNA dodecamer by means of quantum mechanics/molecular mechanics (QM/MM) Car–Parrinello simulations. The free energy of activation required to bring the reactant close together and to form the C–C covalent-bond is estimated to be ∼10 kcal/mol. We observe that the G­[8,5-Me]­T tandem lesion is accommodated with almost no perturbation of the Watson–Crick hydrogen-bond network and induces bend and unwinding angles of ∼20° and 8°, respectively. This rather small structural distortion of the DNA macromolecule compared to other well characterized intrastrand cross-links, such as cyclobutane pyrimidines dimers or cisplatin-DNA complex adduct, is a probable rationale for the known lack of efficient repair of oxidative damages.