Peroxidase self-inactivation in prostaglandin H synthase-1 pretreated with cyclooxygenase inhibitors or substituted with mangano protoporphyrin IX

J Biol Chem. 2001 Jun 8;276(23):19879-88. doi: 10.1074/jbc.M100628200. Epub 2001 Mar 14.

Abstract

Self-inactivation imposes an upper limit on bioactive prostanoid synthesis by prostaglandin H synthase (PGHS). Inactivation of PGHS peroxidase activity has been found to begin with Intermediate II, which contains a tyrosyl radical. The structure of this radical is altered by cyclooxygenase inhibitors, such as indomethacin and flurbiprofen, and by replacement of heme by manganese protoporphyrin IX (forming MnPGHS-1). Peroxidase self-inactivation in inhibitor-treated PGHS-1 and MnPGHS-1 was characterized by stopped-flow spectroscopic techniques and by chromatographic and mass spectrometric analysis of the metalloporphyrin. The rate of peroxidase inactivation was about 0.3 s(-)1 in inhibitor-treated PGHS-1 and much slower in MnPGHS-1 (0.05 s(-)1); as with PGHS-1 itself, the peroxidase inactivation rates were independent of peroxide concentration and structure, consistent with an inactivation process beginning with Intermediate II. The changes in metalloporphyrin absorbance spectra during inactivation of inhibitor-treated PGHS-1 were similar to those observed with PGHS-1 but were rather distinct in MnPGHS-1; the kinetics of the spectral transition from Intermediate II to the next species were comparable to the inactivation kinetics in each case. In contrast to the situation with PGHS-1 itself, significant amounts of heme degradation occurred during inactivation of inhibitor-treated PGHS-1, producing iron chlorin and heme-protein adduct species. Structural perturbations at the peroxidase site (MnPGHS-1) or at the cyclooxygenase site (inhibitor-treated PGHS-1) thus can influence markedly the kinetics and the chemistry of PGHS-1 peroxidase inactivation.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Chromatography, High Pressure Liquid
  • Cyclooxygenase 1
  • Cyclooxygenase Inhibitors / pharmacology*
  • Flurbiprofen / pharmacology
  • Heme / chemistry
  • Indomethacin / pharmacology
  • Isoenzymes / antagonists & inhibitors*
  • Isoenzymes / chemistry
  • Isoenzymes / metabolism
  • Kinetics
  • Peroxidases / antagonists & inhibitors*
  • Prostaglandin-Endoperoxide Synthases / chemistry
  • Prostaglandin-Endoperoxide Synthases / metabolism
  • Protein Conformation
  • Protoporphyrins / chemistry*
  • Spectrometry, Mass, Electrospray Ionization

Substances

  • Cyclooxygenase Inhibitors
  • Isoenzymes
  • Protoporphyrins
  • manganese protoporphyrin
  • Heme
  • Flurbiprofen
  • Peroxidases
  • Cyclooxygenase 1
  • Prostaglandin-Endoperoxide Synthases
  • Indomethacin