Abstract
The stability of triple helical complexes of pyrimidine oligodeoxyribonucleotides containing one abasic 1,2-dideoxy-D-ribose (phi) residue was examined by affinity cleaving. Within a pyrimidine third strand, the triplets phi.AT, phi.GC, phi.TA and phi.CG are significantly less stable than the triplets, T.AT, C+GC and G.TA. The decrease in binding produced by an abasic residue is similar to that observed with imperfectly matched natural base triplets, with phi.AT and phi.GC being less stable than phi.TA and phi.CG triplets for the sequences studied.
MeSH Terms
Base Composition
Base Sequence
Binding Sites
Deoxyribose/analogs & derivatives
Edetic Acid
Molecular Sequence Data
Nucleic Acid Conformation
Oligodeoxyribonucleotides/chemistry
Pyrimidines/chemistry
Chemicals
Oligodeoxyribonucleotides
Pyrimidines
Deoxyribose
1,2-dideoxyribose
Edetic Acid
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Horne D A
Arnold and Mabel Beckman Laboratory of Chemical Synthesis, California Institute of Technology, Pasadena 91125.
Dervan P B
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