Preparation of a novel psoralen containing deoxyadenosine building block for the facile solid phase synthesis of psoralen-modified oligonucleotides for a sequence specific crosslink to a given target sequence

Nucleic Acids Res. 1989 Nov 25;17(22):8967-78. doi: 10.1093/nar/17.22.8967.

Abstract

4,5',8-Trimethylpsoralen was attached to the C8-position of deoxyadenosine via a sulfur atom and a five carbon atom linker. The modified deoxyadenosine was then converted to a protected phosphoramidite and used as unusual as a building block for solid phase oligodeoxyribonucleotide synthesis. The efficiency of the photoreaction of a psoralen-modified oligonucleotide to a complementary matrix strand reached more than 90% within a 1 hour irradiation time at a wavelength of 345 nm.

MeSH terms

  • Base Sequence
  • Cross-Linking Reagents / chemical synthesis*
  • Deoxyadenosines*
  • Furocoumarins*
  • Indicators and Reagents
  • Kinetics
  • Magnetic Resonance Spectroscopy
  • Molecular Sequence Data
  • Oligodeoxyribonucleotides*
  • Spectrometry, Fluorescence
  • Trioxsalen*

Substances

  • Cross-Linking Reagents
  • Deoxyadenosines
  • Furocoumarins
  • Indicators and Reagents
  • Oligodeoxyribonucleotides
  • Trioxsalen