Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10800175 | Biochimica et Biophysica Acta (BBA) - General Subjects | 2014 | 12 Pages |
Abstract
Quantitative measurement of protein oxidation and glycation adducts provides information on level of exposure to potentially damaging protein modifications, protein inactivation in ageing and disease, metabolic control, protein turnover, renal function and other aspects of body function. Reliable and clinically assessable analysis is required for translation of measurement to clinical diagnostic use. Stable isotopic dilution analysis LC-MS/MS provides a “gold standard” approach and reference methodology to which other higher throughput methods such as immunoassay and indirect methods are preferably corroborated by researchers and those commercialising diagnostic kits and reagents. This article is part of a Special Issue entitled Current methods to study reactive oxygen species - pros and cons and biophysics of membrane proteins. Guest Editor: Christine Winterbourn.
Keywords
MG-H1UPLCFCRAOPPCML3-NT6-aminoquinolyl-N-hydroxysuccinimidyl carbamateSAFAASACRFN-formylkynurenineNFKMetSOAminoadipic SemialdehydeBNXmatrix assisted laser desorption ionisationNε-carboxymethyl-lysinefructosamine-3-kinaseMRMGSAMSRESIAQCCelTFA3-nitrotyrosineLC-MS/MSskin autofluorescenceTrifluoroacetic acidProtein oxidationOxidative stressPeritoneal dialysisAgeMethionine sulfoxideGoldMass spectrometryLiquid chromatography-tandem mass spectrometryMoldlow density lipoproteinLDLMALDIMethylglyoxalmethionine sulfoxide reductaseChronic renal failuremultiple reaction monitoringBilateral nephrectomyglutamic semialdehydeHemodialysisAdvanced glycation endproductadvanced oxidation protein productUltra High Performance Liquid ChromatographyProtein glycationbulelectrospray ionisation
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Authors
Paul J. Thornalley, Naila Rabbani,