Abstract
In the light of the biological significance of thymine photodimers , studies of the energetics of the dodecanucleotide fragment d( CGCGAATTCGCG )2 have been carried out using the methods of molecular mechanics, with and without incorporation of a thymine dimer in the cis-syn configuration. The results of the calculations suggest that the thymine dimerized structures show no gross distortion in the double helix with the conformational changes relative to the normal B-DNA double helix restricted largely to the dimer region. The energetics of dTp[]dT reveal a number of conformers which are energetically almost equally favorable and are, as a group, qualitatively consistent with NMR studies on this molecule. The biological implications of the results of the conformational studies, reported here, have been examined vis-a-vis the currently available models for the recognition of DNA "damage" by repair enzymes.
MeSH Terms
DNA
Hydrogen Bonding
Models, Molecular
Nucleic Acid Conformation
Oligodeoxyribonucleotides
Oligonucleotides
Photochemistry
Pyrimidine Dimers
Thermodynamics
Chemicals
Oligodeoxyribonucleotides
Oligonucleotides
Pyrimidine Dimers
DNA
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Rao S N
Keepers J W
Kollman P
References (12)
12 references, click to expand
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