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X-ray structure of a DNA decamer containing 7,8-dihydro-8-oxoguanine.
Author(s) -
Leigh Ann Lipscomb,
Mary Elizabeth Peek,
Marshall Morningstar,
S M Verghis,
Elizabeth M. Miller,
Alexander Rich,
John M. Essigmann,
Loren Dean Williams
Publication year - 1995
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.92.3.719
Subject(s) - deoxyribose , glycosidic bond , steric effects , chemistry , dna , hydrogen bond , stereochemistry , crystallography , duplex (building) , base pair , guanosine , molecule , enzyme , biochemistry , organic chemistry
We have determined the x-ray structure of a DNA fragment containing 7,8-dihydro-8-oxoguanine (G(O)). The structure of the duplex form of d(CCAGOCGCTGG) has been determined to 1.6-A resolution. The results demonstrate that GO forms Watson-Crick base pairs with the opposite C and that G(O) is in the anti conformation. Structural perturbations induced by C.G(O)anti base pairs are subtle. The structure allows us to identify probable elements by which the DNA repair protein MutM recognizes its substrates. Hydrogen bond donors/acceptors within the major groove are the most likely element. In that groove, the pattern of hydrogen-bond donors/acceptors of C.G(O)anti is unique. Additional structural analysis indicates that conversion of G to G(O) would not significantly influence the glycosidic torsion preference of the nucleoside. There is no steric interaction of the 8-oxygen of G(O) with the phospho-deoxyribose backbone.

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