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Principal component analysis of mass spectra of peptides generated from the tryptic digestion of protein mixtures
Author(s) -
Bryant Duncan K.,
Monté Soraya,
Man Wai J.,
Kramer Kerstin,
Bugelski Peter,
Neville William,
White Ian R.,
Camilleri Patrick
Publication year - 2001
Publication title -
rapid communications in mass spectrometry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.528
H-Index - 136
eISSN - 1097-0231
pISSN - 0951-4198
DOI - 10.1002/rcm.247
Subject(s) - chemistry , chromatography , peptide , digestion (alchemy) , mass spectrometry , principal component analysis , polyacrylamide gel electrophoresis , bottom up proteomics , sample preparation in mass spectrometry , biochemistry , enzyme , protein mass spectrometry , tandem mass spectrometry , electrospray ionization , artificial intelligence , computer science
Principal component analysis (PCA) has been used to analyse mass spectral peptide profiles obtained from the enzymatic digestion of standard protein mixtures. Scores and loadings plots clearly revealed peptide fragments that differentiated one protein mixture from another. Peptide map search results identified with a high degree of certainty any additional proteins in these mixtures. As a proof‐of‐concept this methodology was applied to hepatic protein mixtures obtained from rats treated with two hepatotoxic compounds: methapyriline and SB‐219994. Liver proteins were extracted, pre‐separated by one‐dimensional polyacrylamide gel electrophoresis, subjected to tryptic digestion and analysed by mass spectrometry. Two up‐regulated proteins, glutathione S ‐transferase with methapyrilene and peroxisomal bifunctional enzyme with SB‐219994, were identified in this manner. Copyright © 2001 John Wiley & Sons, Ltd.
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