Protein Information

ID 414
Name myeloperoxidase
Synonyms 38 kDa MYELOPEROXIDASE; MPO; Myeloperoxidase; Myeloperoxidase precursor; Peroxidase (Myeloperoxidase); Myeloperoxidases; Myeloperoxidase precursors; Peroxidase (Myeloperoxidase)s

Compound Information

ID 615
Name sodium azide
CAS sodium azide

Reference

PubMed Abstract RScore(About this table)
19345674 Tomono S, Miyoshi N, Sato K, Ohba Y, Ohshima H: Formation of cholesterol ozonolysis products through an ozone-free mechanism mediated by the myeloperoxidase-H2O2-chloride system. Biochem Biophys Res Commun. 2009 May 29;383(2):222-7. Epub 2009 Apr 5.
The presence of the cholesterol ozonolysis products, 3beta-hydroxy-5-oxo-5,6-secocholestan-6-al (atheronal-A) and its aldolization product 3beta-hydroxy-5beta-hydroxy-B-norcholestane-6beta-carboxaldehyde (atheronal-B) in human atherosclerotic tissues was recently reported as evidence for the generation of ozone by activated human neutrophils. However, the mechanism for the formation of atheronals in atherosclerotic tissues is unknown. In this study, we found that atheronals were formed by the reaction of cholesterol with human myeloperoxidase (MPO) in the presence of its substrates H (2) O (2) and Cl (-). The omission of either H (2) O (2) or Cl (-) from the MPO-H (2) O (2)-Cl (-) system resulted in a significant reduction in yields. The formation of atheronals by the MPO-H (2) O (2)-Cl (-) system was inhibited by an inhibitor of MPO and scavengers of reactive oxygen species such as sodium azide, methionine, beta-carotene, and vinylbenzoic acid. Our results suggest that MPO produces atheronals at least partly through an ozone-free mechanism, via the reaction of cholesterol with singlet oxygen generated from HOCl and H (2) O (2).
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