Electron photodetachment dissociation of DNA polyanions in a quadrupole ion trap mass spectrometer

被引:94
作者
Gabelica, Valerie
Tabarin, Thibault
Antoine, Rodolphe
Rosu, Frederic
Compagnon, Isabelle
Broyer, Michel
De Pauw, Edwin
Dugourd, Philippe
机构
[1] Univ Liege, Lab Spectrometrie Masse, Inst Chim, B-4000 Liege, Belgium
[2] Univ Lyon 1, CNRS, UMR 5579, Spectrometrie Ion & Mol Lab, F-69622 Villeurbanne, France
关键词
D O I
10.1021/ac060753p
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
We hereby explore the effects of irradiating DNA polyanions stored in a quadrupole ion trap mass spectrometer with an optical parametric oscillator laser between 250 and 285 nm. We studied DNA 6-20-mer single strands and 12-base pair double strands. In all cases, laser irradiation causes electron detachment from the multiply charged DNA anions. Electron photodetachment efficiency directly depends on the number of guanines in the strand, and maximum efficiency is observed between 260 and 275 nm. Subsequent collision-induced dissociation ( CID) of the radical anions produced by electron photodetachment results in extensive fragmentation. In addition to neutral losses, a large number of fragments from the w, d, a., and z. ion series are obtained, contrasting with the w and (a-base) ion series observed in regular CID. The major advantage of this technique, coined electron photodetachment dissociation (EPD) is the absence of internal fragments, combined with good sequence coverage. EPD is therefore a highly promising approach for de novo sequencing of oligonucleotides. EPD of nucleic acids is also expected to give specific radical-induced strand cleavages, with conservation of other fragile bonds, including noncovalent bonds. In effect, preliminary results on a DNA hairpin and on double strands suggest that EPD could also be used to probe intra- and intermolecular interactions in nucleic acids.
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收藏
页码:6564 / 6572
页数:9
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