High resolution is not a strict requirement for characterization and quantification of histone post-translational modifications

Journal of Proteome Research

Volumn 13, Issue 12, 2014, Pages 6152-6159

  Karch, Kelly R ^a   Zee, Barry M ^b   Garcia, Benjamin A ^a  

^a UNIVERSITY OF PENNSYLVANIA   (United States)

^b PRINCETON UNIVERSITY   (United States)

Author keywords

chromatin; epigenetics; histone; mass spectrometry; modification; proteomics; PTM; quantification; stable isotope

Indexed keywords

ACCURACY; ACETYLATION; ARTICLE; COMPARATIVE STUDY; CONTROLLED STUDY; HISTONE MODIFICATION; HUMAN; HUMAN CELL; ISOTOPE LABELING; MASS SPECTROMETER; MASS SPECTROMETRY; METHYLATION; PROTEIN ANALYSIS; PROTEIN PROCESSING; QUANTITATIVE ANALYSIS; AMINO ACID SEQUENCE; DEVICES; HELA CELL LINE; LIQUID CHROMATOGRAPHY; METABOLISM; PROCEDURES; PROTEOMICS; REPRODUCIBILITY; TANDEM MASS SPECTROMETRY;

HISTONE; LYSINE; PEPTIDE;

ACETYLATION; AMINO ACID SEQUENCE; CHROMATOGRAPHY, LIQUID; HELA CELLS; HISTONES; HUMANS; LYSINE; MASS SPECTROMETRY; METHYLATION; PEPTIDES; PROTEIN PROCESSING, POST-TRANSLATIONAL; PROTEOMICS; REPRODUCIBILITY OF RESULTS; TANDEM MASS SPECTROMETRY;

EID: 84915782631     PISSN: 15353893     EISSN: 15353907     Source Type: Journal    
DOI: 10.1021/pr500902f     Document Type: Article

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