Non-Direct Sequence Ions in the Tandem Mass Spectrometry of Protonated Peptide Amides - an Energy-Resolved Study
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BRONZE
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Yes
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0
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3
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No
Abstract
The fragmentation reactions of the MH+ ions of Leu-enkephalin amide and a variety of heptapeptide amides have been studied in detail as a function of collision energy using a QqToF beam type mass spectrometer. The initial fragmentation of the protonated amides involves primarily formation of bn ions, including significant loss of NH3 from the MH+ ions. Further fragmentation of these bn ions occurs following macrocyclization/ring opening leading in many cases to bn ions with permuted sequences and, thus, to formation of non-direct sequence ions. The importance of these non-direct sequence ions increases markedly with increasing collision energy, making peptide sequence determination difficult, if not impossible, at higher collision energies. [Figure not available: see fulltext.]
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Keywords
Non-direct sequence ions, Peptide amides, Tandem mass spectrometry, Ions, Ions, Molecular Weight, Peptide amides, Spectrometry, Mass, Electrospray Ionization, Tandem mass spectrometry, Tandem Mass Spectrometry, Non-direct sequence ions, Protons, Amides, Oligopeptides
Fields of Science
01 natural sciences, 0104 chemical sciences
Citation
Harrison, A.G., Taşoğlu, Ç., and Yalçın, T. (2013). Non-direct sequence ions in the tandem mass spectrometry of protonated peptide amides - An energy-resolved study. Journal of the American Society for Mass Spectrometry, 24(10), 1565-1572. doi:10.1007/s13361-013-0707-9
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OpenCitations Citation Count
5
Volume
24
Issue
10
Start Page
1565
End Page
1572
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Scopus : 5
PubMed : 2
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