Disruption of heme-peptide covalent cross-linking in mammalian peroxidases by hypochlorous acid

J Inorg Biochem. 2014 Nov:140:245-54. doi: 10.1016/j.jinorgbio.2014.06.018. Epub 2014 Jul 8.

Abstract

Myeloperoxidase (MPO), lactoperoxidase (LPO) and eosinophil peroxidase (EPO) play a central role in oxidative damage in inflammatory disorders by utilizing hydrogen peroxide and halides/pseudo halides to generate the corresponding hypohalous acid. The catalytic sites of these enzymes contain a covalently modified heme group, which is tethered to the polypeptide chain at two ester linkages via the methyl group (MPO, EPO and LPO) and one sulfonium bond via the vinyl group (MPO only). Covalent cross-linking of the catalytic site heme to the polypeptide chain in peroxidases is thought to play a protective role, since it renders the heme moiety less susceptible to the oxidants generated by these enzymes. Mass-spectrometric analysis revealed the following possible pathways by which hypochlorous acid (HOCl) disrupts the heme-protein cross-linking: (1) the methyl-ester bond is cleaved to form an alcohol; (2) the alcohol group undergoes an oxygen elimination reaction via the formation of an aldehyde intermediate or undergoes a demethylation reaction to lose the terminal CH2 group; and (3) the oxidative cleavage of the vinyl-sulfonium linkage. Once the heme moiety is released it undergoes cleavage at the carbon-methyne bridge either along the δ-β or a α-γ axis to form different pyrrole derivatives. These results indicate that covalent cross-linking is not enough to protect the enzymes from HOCl mediated heme destruction and free iron release. Thus, the interactions of mammalian peroxidases with HOCl modulates their activity and sets a stage for initiation of the Fenton reaction, further perpetuating oxidative damage at sites of inflammation.

Keywords: Heme destruction; Hypochlorous acid; Inflammation; Mammalian peroxidase; Oxidative stress.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Biocatalysis
  • Chromatography, Liquid
  • Heme / chemistry*
  • Humans
  • Hypochlorous Acid / chemistry*
  • Oxidative Stress
  • Peptides / chemistry*
  • Peroxidases / chemistry*
  • Spectrometry, Mass, Electrospray Ionization

Substances

  • Peptides
  • Heme
  • Hypochlorous Acid
  • Peroxidases