Silver(I)-mediated cytosine self-pairing is preferred over hoogsteen-type base pairs with the artificial nucleobase 1,3-dideaza-6-nitropurine

Nucleosides Nucleotides Nucleic Acids. 2010 Jan;29(1):27-38. doi: 10.1080/15257770903451579.

Abstract

A 2'-deoxyribonucleoside containing 1,3-dideaza-6-nitropurine was synthesized and incorporated into oligonucleotides. The acid-base properties of this nucleoside and the corresponding N9-methylated derivative were investigated by pD-dependent (1)H NMR spectroscopy. A possible formation of Hoogsteen-type base pairs with cytosine was studied by ultraviolet (UV) and circular dichroism (CD) spectroscopy in the presence and absence of Ag(I) and under neutral and acidic conditions, respectively. In each case, no indication for the formation of Hoogsteen-type base pairs was obtained, which is attributed to the higher affinity of cytosine to form self-complementary hemi-protonated base pairs under acidic conditions and metal-mediated homo base pairs in presence of Ag(I), respectively.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Pairing*
  • Base Sequence
  • Benzimidazoles / chemistry*
  • Circular Dichroism
  • Cytosine / metabolism*
  • Hydrogen-Ion Concentration
  • Molecular Sequence Data
  • Nucleic Acid Denaturation
  • Nucleic Acid Heteroduplexes
  • Oligonucleotides / chemistry
  • Oligonucleotides / genetics
  • Purines / chemistry*
  • Silver Nitrate / chemistry*
  • Titrimetry

Substances

  • Benzimidazoles
  • Nucleic Acid Heteroduplexes
  • Oligonucleotides
  • Purines
  • Cytosine
  • Silver Nitrate