Winterbourn Christine C, Kettle Anthony J
Free Radical Research, Department of Pathology, Christchurch School of Medicine and Health Sciences, Christchurch, New Zealand.
Jpn J Infect Dis. 2004 Oct;57(5):S31-3.
Myeloperoxidase (MPO) uses hydrogen peroxide to oxidize chloride to hypochlorous acid. It also converts numerous substrates to reactive free radicals. When released by neutrophils, the enzyme operates in the presence of a flux of superoxide. We show that superoxide has a profound influence on oxidative reactions catalysed by MPO. It reacts directly with the enzyme to modulate production of hypochlorous acid. Within neutrophil phagosomes, where MPO functions to kill micro-organisms, it may be the preferred substrate for the enzyme. Superoxide also reacts rapidly with radicals generated by MPO, e.g. from tyrosine and tyrosyl peptides. Initial products are organic peroxides. These species are likely to be toxic and contribute to the pathophysiological actions of MPO.
髓过氧化物酶(MPO)利用过氧化氢将氯离子氧化为次氯酸。它还能将多种底物转化为活性自由基。当中性粒细胞释放该酶时,它在超氧阴离子流存在的情况下发挥作用。我们发现超氧阴离子对MPO催化的氧化反应有深远影响。它直接与该酶反应以调节次氯酸的生成。在中性粒细胞吞噬体中,MPO发挥杀灭微生物的作用,超氧阴离子可能是该酶的首选底物。超氧阴离子还能迅速与MPO产生的自由基反应,例如来自酪氨酸和酪氨酰肽的自由基。初始产物是有机过氧化物。这些物质可能具有毒性,并有助于MPO的病理生理作用。