Screening assay for the identification of deoxyhypusine synthase inhibitors

J Biomol Screen. 2004 Aug;9(5):434-8. doi: 10.1177/1087057104264031.

Abstract

The 1st step in the posttranslational hypusine [N(epsilon)-(4-amino-2-hydroxybutyl)lysine] modification of eukaryotic translation initiation factor 5A (eIF5A) is catalyzed by deoxyhypusine synthase (DHS). The eIF5A intermediate is subsequently hydroxylated by deoxyhypusine hydroxylase (DHH), thereby converting the eIF5A precursor into a biologically active protein. Depletion of eIF5A causes inhibition of cell growth, and the identification of eIF5A as a cofactor of the HIV Rev protein turns this host protein and therefore DHS into an interesting target for drugs against abnormal cell growth and/or HIV replication. The authors developed a 96-well format DHS assay applicable for the screening of DHS inhibitors. Using this assay, they demonstrate DHS inhibition by AXD455 (Semapimod, CNI-1493). This assay represents a powerful tool for the identification of new DHS inhibitors with potency against cancer and HIV.

MeSH terms

  • Electrophoresis, Polyacrylamide Gel
  • Enzyme Inhibitors / chemistry*
  • Enzyme Inhibitors / pharmacology
  • Eukaryotic Translation Initiation Factor 5A
  • Hydrazones / chemistry*
  • Hydrazones / pharmacology
  • Oxidoreductases Acting on CH-NH Group Donors / antagonists & inhibitors*
  • Oxidoreductases Acting on CH-NH Group Donors / isolation & purification
  • Peptide Initiation Factors / isolation & purification
  • RNA-Binding Proteins / isolation & purification
  • Recombinant Proteins / antagonists & inhibitors
  • Recombinant Proteins / isolation & purification

Substances

  • Enzyme Inhibitors
  • Hydrazones
  • Peptide Initiation Factors
  • RNA-Binding Proteins
  • Recombinant Proteins
  • semapimod
  • Oxidoreductases Acting on CH-NH Group Donors
  • deoxyhypusine synthase