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HERO ID
5198409
Reference Type
Journal Article
Title
Protein sequencing by tandem mass spectrometry
Author(s)
Hunt, DF; Yates, JR; Shabanowitz, J; Winston, S; Hauer, CR
Year
1986
Is Peer Reviewed?
1
Journal
Proceedings of the National Academy of Sciences of the United States of America
ISSN:
0027-8424
EISSN:
1091-6490
Volume
83
Issue
17
Page Numbers
6233-6237
Language
English
PMID
3462691
DOI
10.1073/pnas.83.17.6233
Abstract
Methodology for determining amino acid sequences of proteins by tandem mass spectrometry is described. The approach involves enzymatic and/or chemical degradation of the protein to a collection of peptides which are then fractionated by high-performance liquid chromatography. Each fraction, containing as many as 10-15 peptides, is then analyzed directly, without further purification, by a combination of liquid secondary-ion/collision-activated dissociation mass spectrometry on a multianalyzer instrument. Interpretation of collision-activated dissociation mass spectra is described, and results are presented from a study of soluble peptides produced by treatment of apolipoprotein B with cyanogen bromide and trypsin.
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