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• W2896618552 abstract "Enzymatic 18O exchange, the well-established approach in comparative proteomics, has some disadvantages such as back exchange of labeled oxygen and overlapping the peak of a labeled peptide with isotopic peaks of an unlabeled one. Herein we demonstrated a simple procedure in which samples digested with a trypsin (with and without H218O) were reacted with unlabeled and quadrupled 13C-labeled pyrylium salt respectively which results in formation of pyridinium cations. Thus, each isobarically labeled peptide containing zero or four 13C atoms in the mass reporter group, during tandem MS/MS forms an unique reporter ion useful for a relative quantitation. Such a sample treatment improves the signal to noise ratio, reduces overlapping of the isotopic peaks and completely eliminates the back exchange problem." @default.
• W2896618552 created "2018-10-26" @default.
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• W2896618552 date "2019-02-01" @default.
• W2896618552 modified "2023-10-05" @default.
• W2896618552 title "Isobaric duplex based on a combination of 16O/18O enzymatic exchange and labeling with pyrylium salts" @default.
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• W2896618552 doi "https://doi.org/10.1016/j.aca.2018.10.012" @default.
• W2896618552 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30598162" @default.
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