Study of the mass spectrometric fragmentation of pseudouridine:: comparison of fragmentation data obtained by matrix-assisted laser desorption/ionisation post-source decay, electrospray ion trap multistage mass spectrometry, and by a method utilising electrospray quadrupole time-of-flight tandem mass spectrometry and in-source fragmentation

被引:37
作者
Dudley, E
Tuytten, R
Bond, A
Lemière, F
Brenton, AG
Esmans, EL
Newton, RP
机构
[1] Univ Wales Swansea, Biomol Anal Mass Spectrometry Facil, Swansea SA2 8PP, W Glam, Wales
[2] Univ Antwerp, Dept Chem, Nucleoside Res & Mass Spectrometry Unit, B-2020 Antwerp, Belgium
[3] Univ Wales Swansea, Biochem Grp, Swansea SA2 8PP, W Glam, Wales
[4] Univ Wales Swansea, Dept Chem, Mass Spectrometry Res Unit, Swansea SA2 8PP, W Glam, Wales
[5] Univ Antwerp, Ctr Proteome Anal & Mass Spectrometry, B-2020 Antwerp, Belgium
关键词
D O I
10.1002/rcm.2151
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Many nucleosides and their modified forms have been studied by mass spectrometry elaborating the detailed fragmentation pathways under MS2 and MSn conditions. Although the C-nucleoside pseudouridine has been fragmented and studied briefly, usually amongst many other nucleosides, it has not been investigated to the same extent as other nucleosides. In this report a number of different mass spectrometric techniques are applied to obtain a fuller picture of pseudouridine fragmentation. At the same time this study is used to compare different tandem mass spectrometric techniques, including a novel methodology utilising a quadrupole time-of-flight (Q-ToF) instrument for MSn analysis comparable with that available with an ion trap mass spectrometer. Copyright (C) 2005 John Wiley & Sons, Ltd.
引用
收藏
页码:3075 / 3085
页数:11
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