Electron‐Capture‐Induced Dissociation of Microsolvated Di‐ and Tripeptide Monocations: Elucidation of Fragmentation Channels from Measurements of Negative Ions

The branching ratio between ammonia loss and NCα bond cleavage of singly charged microsolvated peptides after electron capture from cesium depends on the solvent molecule attached. Density functional calculations reveal that for [GA+H]+(CE) (G=glycine, A=alanine, CE=crown ether), the singly occupie...

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Veröffentlicht in:Chemphyschem 2009-07, Vol.10 (9‐10), p.1619-1623
Hauptverfasser: Zettergren, Henning, Adoui, Lamri, Bernigaud, Virgile, Cederquist, Henrik, Haag, Nicole, Holm, Anne I. S., Huber, Bernd A., Hvelplund, Preben, Johansson, Henrik, Kadhane, Umesh, Koefoed Larsen, Mikkel, Liu, Bo, Manil, Bruno, Brøndsted Nielsen, Steen, Panja, Subhasis, Rangama, Jimmy, Reinhed, Peter, Schmidt, Henning T., Støchkel, Kristian
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Sprache:eng
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Zusammenfassung:The branching ratio between ammonia loss and NCα bond cleavage of singly charged microsolvated peptides after electron capture from cesium depends on the solvent molecule attached. Density functional calculations reveal that for [GA+H]+(CE) (G=glycine, A=alanine, CE=crown ether), the singly occupied molecular orbital of the neutral radical is located mainly on the amide group (see picture). The results from an experimental study of bare and microsolvated peptide monocations in high‐energy collisions with cesium vapor are reported. Neutral radicals form after electron capture from cesium, which decay by H loss, NH3 loss, or NCα bond cleavage into characteristic z. and c fragments. The neutral fragments are converted into negatively charged species in a second collision with cesium and are identified by means of mass spectrometry. For protonated GA (G=glycine, A=alanine), the branching ratio between NH3 loss and NCα bond cleavage is found to strongly depend on the molecule attached (H2O, CH3CN, CH3OH, and 18‐crown‐6 ether (CE)). Addition of H2O and CH3OH increases this ratio whereas CH3CN and CE decrease it. For protonated AAA ([AAA+H]+), a similar effect is observed with methanol, while the ratio between the z1 and z2 fragment peaks remains unchanged for the bare and microsolvated species. Density functional theory calculations reveal that in the case of [GA+H]+(CE), the singly occupied molecular orbital is located mainly on the amide group in accordance with the experimental results. The branching ratio between ammonia loss and NCα bond cleavage of singly charged microsolvated peptides after electron capture from cesium depends on the solvent molecule attached. Density functional calculations reveal that for [GA+H]+(CE) (G=glycine, A=alanine, CE=crown ether), the singly occupied molecular orbital of the neutral radical is located mainly on the amide group (see picture).
ISSN:1439-4235
1439-7641
DOI:10.1002/cphc.200800782