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Nucleic Acids Research, Vol 27, Issue 17 3550-3556, Copyright © 1999 by Oxford University Press


ARTICLES

Probing the role of structural water in a duplex oligodeoxyribonucleotide containing a water-mimicking base analog

D Kosztin, RI Gumport and K Schulten
Department of Chemistry, University of Illinois, Urbana, Champaign, 61801, USA.

Molecular dynamics simulations were performed on models of the dodecamer DNA double-stranded segment, [d(CGCGAATTCGCG)](2), in which each of the adenine residues, individually or jointly, was replaced by the water-mimicking analog 2'-deoxy-7-(hydroxy-methyl)-7-deazaadenosine (hm(7)c(7)dA) [Rockhill, J.K., Wilson,S.R. and Gumport,R.I. (1996) J. Am. Chem. Soc.,118, 10065-10068]. The simulations, when compared with those of the dodecamer itself, show that incorporation of the analog affects neither the overall DNA structure nor its hydrogen-bonding and stacking interactions when it replaces a single individual base. Furthermore, the water molecules near the bases in the singly- substituted oligonucleotides are similarly unaffected. Double substitutions lead to differences in all the aforementioned parameters with respect to the reference sequence. The results suggest that the analog provides a good mimic of specific 'ordered' water molecules observed in contact with DNA itself and at the interface between protein and DNA in specific complexes.
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J. Yu, T. Ha, and K. Schulten
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