Mass Spectrum Patterns of 18O-Tagged Peptides Labeled by Enzyme-Catalyzed Oxygen Exchange
Author:
Affiliation:
1. Bioinformatics Department, Center for Genetic Engineering and Biotechnology, P.O. Box 6162, CP 10600, C. Habana, Cuba
Publisher
American Chemical Society (ACS)
Subject
Analytical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ac1025368
Reference24 articles.
1. Preparation of stable isotope-incorporated peptide internal standards for field desorption mass spectrometry quantification of peptides in biologic tissue
2. Facile assignment of sequence ions of a peptide labelled with18O at the carboxyl terminus
3. A method for determination of N-glycosylation sites in glycoproteins by collision-induced dissociation analysis in fast atom bombardment mass spectrometry: Identification of the positions of carbohydrate-linked asparagine in recombinant α-amylase by treatment with peptide-N-glycosidase F in 18O-labeled water
4. C-terminal peptide identification by fast atom bombardment mass spectrometry
5. 18O-Labeling of N-Glycosylation Sites To Improve the Identification of Gel-Separated Glycoproteins Using Peptide Mass Mapping and Database Searching
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1. O18Quant: A Semiautomatic Strategy for Quantitative Analysis of High-Resolution16O/18O Labeled Data;BioMed Research International;2014
2. Mechanistic insights into 1-deoxy-d-xylulose 5-phosphate reductoisomerase, a key enzyme of the MEP terpenoid biosynthetic pathway;FEBS Journal;2013-10-24
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