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Structures, stabilities & conformational behaviors of hydrogen-atom abstractions of cytosine nucleosides: AIM & NBO analysis.

Authors :
Tehrani, Zahra Aliakbar
Javan, Marjan Jebeli
Fattahi, Alireza
Hashemi, Mohammad Mahmoodi
Source :
Computational & Theoretical Chemistry; Sep2011, Vol. 971 Issue 1-3, p19-29, 11p
Publication Year :
2011

Abstract

Abstract: Abstraction of hydrogen atom from DNA and RNA subunits leads to formation of a neutral radical. The formation of these radicals can lead to harmful structural alternations and formation of multiple lesions in helixes of DNA and RNA. In the present work, we explore theoretically energetic and structural properties of the possible radicals formed via hydrogen atom abstraction at various sites of sugar part of cytosine nucleosides by employing B3LYP exchange–correlation functional with 6-311++G (d,p) orbital basis sets. Two types of free radicals may be found by hydrogen abstraction of sugar part of cytosine nucleosides: carbon centered radicals and the oxygen centered radicals. The computation revealed 0–22.6kcal/mol energy disparity in these radical. Radical-centered carbon increases the extent of bonding with its adjacent atoms. This tendency should be important in predicting the reactivity of sugar-based radicals. The hydrogen abstracted sugar radicals of cytosine nucleosides have following stability sequence: raC2 ′> raC1 ′> raC3 ′> raC4 ′> raC5 ′> raO5 ′> raO2 ′> raO3 ′ for cytidine and radC1 ′> radC2 ′> radC4 ′> radC3 ′> radC5 ′> radO5 ′> radO3 ′ for deoxycytidine. Furthermore, to take into account the effect of solvent environment on the stability order of radicals integral equation formalism of the polarized continuum model (IEF-PCM) was employed to model aqueous solution. The role of CH⋯O and HO⋯H intramolecular hydrogen bonds in stability of radicals investigated based on results of topological properties of AIM theory. Moreover, variations of significant structural parameters such as puckering amplitudes and phase angles of sugar parts of cytosine nucleosides after radical formation are also found. These finding have several biological implications and may explain the possible degrees of damage to the DNA double strand. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
2210271X
Volume :
971
Issue :
1-3
Database :
Supplemental Index
Journal :
Computational & Theoretical Chemistry
Publication Type :
Academic Journal
Accession number :
64862439
Full Text :
https://doi.org/10.1016/j.comptc.2011.05.033