Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
10
pubmed:dateCreated
2002-10-4
pubmed:abstractText
In this study, we investigated the effects of various nitrogen oxide (NO(x)) species on the extent of prostaglandin H(2) synthase-1 (PGHS-1) nitration in purified protein and in vascular smooth muscle cells. We also examined PGHS-1 activity under these conditions and found the degree of nitration to correlate inversely with enzyme activity. In addition, since NO(x) species are thought to invoke damage during the pathogenesis of atherosclerosis, we examined human atheromatous tissue for PGHS-1 nitration. Both peroxynitrite and tetranitromethane induced Tyr nitration of purified PGHS-1, whereas 1-hydroxy-2-oxo-3-(N-methyl-aminopropyl)-3-methyl-1-triazene (NOC-7; a nitric oxide-releasing compound) did not. Smooth muscle cells treated with peroxynitrite showed PGHS-1 nitration. The extent of nitration by specific NO(x) species was determined by electrospray ionization mass spectrometry. Tetranitromethane was more effective than peroxynitrite, NOC-7, and nitrogen dioxide at nitrating a tyrosine-containing peptide (12%, 5%, 1%, and <1% nitration, respectively). Nitrogen dioxide and, to a lesser extent, peroxynitrite, induced dityrosine formation. Using UV/Vis spectroscopy, it was estimated that the reaction of PGHS-1 with excess peroxynitrite yielded two nitrated tyrosines/PGHS-1 subunit. Finally, atherosclerotic tissue obtained from endarterectomy patients was shown to contain nitrated PGHS-1. Thus, prolonged exposure to elevated levels of peroxynitrite may cause oxidative damage through tyrosine nitration.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
0022-2275
pubmed:author
pubmed:issnType
Print
pubmed:volume
43
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1718-26
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed-meshheading:12364556-Animals, pubmed-meshheading:12364556-Aorta, Thoracic, pubmed-meshheading:12364556-Blotting, Western, pubmed-meshheading:12364556-Culture Techniques, pubmed-meshheading:12364556-Endarterectomy, Carotid, pubmed-meshheading:12364556-Humans, pubmed-meshheading:12364556-Male, pubmed-meshheading:12364556-Muscle, Smooth, Vascular, pubmed-meshheading:12364556-Nitric Oxide Donors, pubmed-meshheading:12364556-Nitrogen Oxides, pubmed-meshheading:12364556-Precipitin Tests, pubmed-meshheading:12364556-Prostaglandin-Endoperoxide Synthases, pubmed-meshheading:12364556-Rats, pubmed-meshheading:12364556-Seminal Vesicles, pubmed-meshheading:12364556-Sheep, pubmed-meshheading:12364556-Spectrometry, Mass, Electrospray Ionization, pubmed-meshheading:12364556-Spectrophotometry, pubmed-meshheading:12364556-Tyrosine
pubmed:year
2002
pubmed:articleTitle
Tyrosine nitration in prostaglandin H(2) synthase.
pubmed:affiliation
Center of Vascular Biology, Weill Medical College of Cornell University, 1300 York Avenue, New York, New York 10021, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't