Structures of b and a product ions from the fragmentation of argentinated peptides
Research output: Journal Publications and Reviews › RGC 21 - Publication in refereed journal › peer-review
Author(s)
Detail(s)
Original language | English |
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Pages (from-to) | 7302-7309 |
Journal / Publication | Journal of the American Chemical Society |
Volume | 120 |
Issue number | 29 |
Publication status | Published - 29 Jul 1998 |
Link(s)
Abstract
Argentinated (silver-containing) oligopeptides fragment under low- energy collision conditions to yield abundant argentinated product ions. The structures of the [b2 - H + Ag]+ and [a2 - H + Ag]+ ions have been determined by means of tandem mass spectrometry and confirmed by comparison with synthesized derivatives of the candidate [b2 - H + Ag]+ ion structure. The [b2 - H + Ag]+ ion was found to be an N-argentinated oxazolone, which could subsequently form the [a2 - H + Ag]+ ion and other product ions after collision activation. Tripeptides containing proline as their second residue were observed to form a relatively less abundant [b2 - H + Ag]+ ion, which was postulated to be an argentinated ketene.
Citation Format(s)
Structures of b and a product ions from the fragmentation of argentinated peptides. / Lee, Vicky W.-M.; Li, Hongbo; Lau, Tai-Chu et al.
In: Journal of the American Chemical Society, Vol. 120, No. 29, 29.07.1998, p. 7302-7309.
In: Journal of the American Chemical Society, Vol. 120, No. 29, 29.07.1998, p. 7302-7309.
Research output: Journal Publications and Reviews › RGC 21 - Publication in refereed journal › peer-review