Uniformly modified 2'-deoxy-2'-fluoro phosphorothioate oligonucleotides as nuclease-resistant antisense compounds with high affinity and specificity for RNA targets

J Med Chem. 1993 Apr 2;36(7):831-41. doi: 10.1021/jm00059a007.


"Uniformly" modified phosphodiester or phosphorothioate oligonucleotides incorporating 2'-deoxy-2'-fluoroadenosine, -guanosine, -uridine, and -cytidine, reported herein for the first time, when hybridized with RNA afforded consistent additive enhancement of duplex stability without compromising base-pair specificity. CD spectra of the 2'-deoxy-2'-fluoro-modified oligonucleotides hybridized with RNA indicated that the duplex adopts a fully A-form conformation. The 2'-deoxy-2'-fluoro-modified oligonucleotides in phosphodiester form were not resistant to nucleases; however, the modified phosphorothioate oligonucleotides were highly nuclease resistant and retained exceptional binding affinity to the RNA targets. The stabilizing effects of the 2'-deoxy-2'-fluoro modifications on RNA-DNA duplexes were shown to be superior to those of the 2'-O-methylribo substitutions. RNA hybrid duplexes with uniformly 2'-deoxy-2'-fluoro-modified oligonucleotides did not support HeLa RNase H activity; however, incorporation of the modifications into "chimeric" oligonucleotides has been shown to activate mammalian RNase H. "Uniformly" modified 2'-deoxy-2'-fluoro phosphorothioate oligonucleotides afforded antisense molecules with (1) high binding affinity and selectivity for the RNA target and (2) stability toward nucleases.

MeSH terms

  • Base Sequence
  • Deoxyribonucleases / drug effects
  • Hydrolysis
  • Molecular Sequence Data
  • Oligonucleotides, Antisense / chemical synthesis*
  • Oligonucleotides, Antisense / pharmacology
  • Ribonucleases / drug effects
  • Structure-Activity Relationship
  • Thermodynamics
  • Thionucleotides / chemical synthesis*
  • Thionucleotides / pharmacology


  • Oligonucleotides, Antisense
  • Thionucleotides
  • Deoxyribonucleases
  • Ribonucleases