• Title of article

    A comparison of flexible and constrained haptens in eliciting antibody catalysts for paraoxon hydrolysis Original Research Article

  • Author/Authors

    David A. Spivak، نويسنده , , Timothy Z. Hoffman، نويسنده , , Alisa H. Moore، نويسنده , , Matthew J. Taylor، نويسنده , , Kim D. Janda and Ian A. Wilson، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 1999
  • Pages
    6
  • From page
    1145
  • To page
    1150
  • Abstract
    A new amine-oxide hapten was employed as an antigen, producing seven monoclonal antibodies (mAbs) from a panel of 20 that catalyzed paraoxon hydrolysis. The current hapten design differs from that previously described in that the molecule is inherently more flexible than its constrained predecessor. One of the seven antibody catalysts, mAb 1H9, showed the highest activity and was selected for detailed study. At pH=8.77, the catalytic hydrolysis of paraoxon by mAb 1H9 followed Michaelis–Menten kinetics affording a kcat=3.73×10−4 min−1 and a Km=1.12 mM with a rate acceleration kcat/kuncat=56. The hapten was found to be a competitive inhibitor of antibody-catalyzed paraoxon hydrolysis with a Ki=0.54 mM. A comparison of both the number and proficiency of antibody catalysts obtained when utilizing a flexible versus constrained hapten indicates that, for paraoxon hydrolysis, constrained haptens elicit superior catalysts, suggesting that further development should begin with the use of constrained haptens in producing more proficient antibody catalysts for paraoxon hydrolysis.
  • Journal title
    Bioorganic and Medicinal Chemistry
  • Serial Year
    1999
  • Journal title
    Bioorganic and Medicinal Chemistry
  • Record number

    1302320