Isotope-coded N-terminal sulfonation of peptides allows quantitative proteomic analysis with increased de novo peptide sequencing capability

Rapid Communications in Mass Spectrometry

Volumn 18, Issue 24, 2004, Pages 3019-3027

  Lee, Yong Ho ^a   Han, Hoon ^b   Chang, Seok Bok ^b   Lee, Sang Won ^a  

^a Korea University   (South Korea)

^b Korea Advanced Institute of Science and Technology (KAIST)   (South Korea)

Author keywords

[No Author keywords available]

Indexed keywords

C (PROGRAMMING LANGUAGE); ISOTOPES; LIQUID CHROMATOGRAPHY; MASS SPECTROMETERS; MASS SPECTROMETRY; MOLECULAR BIOLOGY; SULFONATION;

DE NOVO PEPTIDE SEQUENCING; DE NOVO SEQUENCING; ISOTHIOCYANATES; MASS SPECTROMETRIC ANALYSIS; N-TERMINALS; PEPTIDE MIXTURES; PROTEOMICS; QUANTITATIVE PROTEOMIC ANALYSIS; SULFOPHENYL; SULPHONATION;

PEPTIDES;

CARBON 13; ISOTHIOCYANIC ACID; PEPTIDE; SULFANILIC ACID;

ARTICLE; CHEMICAL STRUCTURE; DERIVATIZATION; FRAGMENTATION REACTION; ISOTOPE LABELING; PROTEIN DEGRADATION; PROTEOMICS; REVERSED PHASE LIQUID CHROMATOGRAPHY; SEQUENCE ANALYSIS; SULFONATION; TANDEM MASS SPECTROMETRY;

EID: 10844282706     PISSN: 09514198     EISSN: None     Source Type: Journal    
DOI: 10.1002/rcm.1724     Document Type: Article

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