[Modified oligonucleotides containing 1-beta-D-galactopyranosylthymine: synthesis and substrate properties]

Bioorg Khim. 2002 Jan-Feb;28(1):56-63.
[Article in Russian]

Abstract

A convenient method of regioselective introduction of 1-beta-D-galactopyranosylthymine into oligonucleotides was developed and the substrate properties of the modified oligonucleotides were investigated in the enzymic reaction of formation and hydrolysis of internucleotide bonds. The English version of the paper.

Publication types

  • English Abstract

MeSH terms

  • Biochemistry / methods*
  • Deoxyribonuclease EcoRI / chemistry
  • Deoxyribonuclease EcoRI / metabolism
  • Deoxyribonucleases, Type II Site-Specific / chemistry
  • Deoxyribonucleases, Type II Site-Specific / metabolism
  • Galactose / analogs & derivatives
  • Galactose / chemistry*
  • Galactose / metabolism*
  • Hydrolysis
  • Magnetic Resonance Spectroscopy
  • Molecular Structure
  • Oligonucleotides / chemistry*
  • Oligonucleotides / metabolism*
  • Structure-Activity Relationship
  • Thymine / analogs & derivatives
  • Thymine / chemistry*
  • Thymine / metabolism*

Substances

  • 1-galactopyranosylthymine
  • Oligonucleotides
  • Deoxyribonuclease EcoRI
  • endodeoxyribonuclease XBAI
  • Deoxyribonucleases, Type II Site-Specific
  • GATATC-specific type II deoxyribonucleases
  • Thymine
  • Galactose