Exploration of a potential difluoromethyl-nucleoside substrate with the fluorinase enzyme

Stephen Thompson, Stephen McMahon, Jim Naismith, David O'Hagan

Research output: Contribution to journalArticlepeer-review

21 Citations (Scopus)

Abstract

The investigation of a difluoromethyl-bearing nucleoside with the fluorinase enzyme is described. 5’,5’–Difluoro-5’-deoxyadenosine 7 (F2DA) was synthesised from adenosine, and found to bind to the fluorinase enzyme by isothermal titration calorimetry with similar affinity compared to 5’–fluoro-5’-deoxyadenosine 2 (FDA), the natural product of the enzymatic reaction. F2DA 7 was found, however, not to undergo the enzyme catalysed reaction with l–selenomethionine, unlike FDA 2, which undergoes reaction with l-selenomethionine to generate Se-adenosylselenomethionine. A co-crystal structure of the fluorinase and F2DA 7 and tartrate was solved to 1.8 Å, and revealed that the difluoromethyl group bridges interactions known to be essential for activation of fluoride for reaction. An unusual hydrogen bonding interaction between the hydrogen of the difluoromethyl group and one of the hydroxyl oxygens of the tartrate ligand was also observed. The bridging interactions, coupled with the inherently stronger C–F bond in the difluoromethyl group, offers an explanation for why no reaction is observed.

Original languageEnglish
JournalBioorganic Chemistry
VolumeIn press
Early online date18 Nov 2015
DOIs
Publication statusPublished - 2015

Keywords

  • Fluorinase
  • Difluoromethyl
  • Isothermal titration calorimetry
  • Protein crystallography

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