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. 2002 Mar;82(3):1554-69.
doi: 10.1016/S0006-3495(02)75507-0.

Intrinsic conformational energetics associated with the glycosyl torsion in DNA: a quantum mechanical study

Nicolas Foloppe  1 , Brigitte Hartmann, Lennart Nilsson, Alexander D MacKerell Jr
Affiliations

Intrinsic conformational energetics associated with the glycosyl torsion in DNA: a quantum mechanical study

Nicolas Foloppe et al. Biophys J. 2002 Mar.

Abstract

The glycosyl torsion (chi) in nucleic acids has long been recognized to be a major determinant of their conformational properties. chi torsional energetics were systematically mapped in deoxyribonucleosides using high-level quantum mechanical methods, for north and south sugar puckers and with gamma in the g(+) and trans conformations. In all cases, the syn conformation is found higher in energy than the anti. When gamma is changed from g(+) to trans, the anti orientation of the base is strongly destabilized, and the energy difference and barrier between anti and syn are significantly decreased. The barrier between anti and syn in deoxyribonucleosides is found to be less than 10 kcal/mol and tends to be lower with purines than with pyrimidines. With gamma = g(+)/chi = anti, a south sugar yields a significantly broader energy well than a north sugar with no energy barrier between chi values typical of A or B DNA. Contrary to the prevailing view, the syn orientation is not more stable with south puckers than with north puckers. The syn conformation is significantly more energetically accessible with guanine than with adenine in 5-nucleotides but not in nucleosides. Analysis of nucleic acid crystal structures shows that gamma = trans/chi = anti is a minor but not negligible conformation. Overall, chi appears to be a very malleable structural parameter with the experimental chi distributions reflecting, to a large extent, the associated intrinsic torsional energetics.

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