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Title: 18O-labeling quantitative proteomics using an ion trap mass spectrometer. Author: Sakai J, Kojima S, Yanagi K, Kanaoka M. Journal: Proteomics; 2005 Jan; 5(1):16-23. PubMed ID: 15744833. Abstract: We describe a method for simultaneous identification and quantitation of proteins within complex mixtures. The method consists of 18O-labeling, a simple stable isotope-coding that requires merely enzymatic digestion in 18O-water, in combination with a capillary-liquid chromatography electrospray ion-trap mass spectrometer. In a separate experiment using the same sample and a spike test, we demonstrate that the difference ration was calculated accurately using the 18O-labeling method even if the protein was part of a complex mixture. Our data also suggest that the accuracy of the quantitation can be improved by averaging the difference ratios of several peptides. In comparing our method with the isotope-coded affinity tag (ICAT) method, we show that the 18O-labeling method has the advantages of better recovery and fewer isotope effects. Therefore, the 18O-labeling method is a powerful tool for large-scale proteomics applications.[Abstract] [Full Text] [Related] [New Search]