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Gas‒phase reactions of NO+with Glu and γ‒Glu–Met
Author(s) -
H. Wincel,
Roel H. Fokkens,
N. M. M. Nibbering
Publication year - 2000
Publication title -
journal of spectroscopy
Language(s) - English
Resource type - Journals
eISSN - 2314-4920
pISSN - 2314-4939
DOI - 10.1155/2000/781283
Subject(s) - chemistry , ion , electrophile , molecule , dipeptide , medicinal chemistry , mass spectrometry , reactivity (psychology) , gas phase , oxygen , stereochemistry , photochemistry , amino acid , organic chemistry , catalysis , medicine , biochemistry , alternative medicine , chromatography , pathology
The reactivity of the nitrosonium ion, NO + , with the amino acid Glu and the dipeptide γ‒Glu–Met in the gas phase has been investigated using the combination of chemical ionisation mass spectrometry and MS/MS. It is shown that NO + reacts efficiently with both Glu and Glu–Met leading to the formation of the nitroso‒group containing ions at m/z 159 and 288. The formation of m/z 159, (GluNO‒18) + , is rationalized by a mechanism involving an electrophilic attack of NO + upon the carbonyl oxygen atom of one of the carboxylic groups of Glu and the N‒terminal carboxylic group of Glu–Met leading to the neutral losses of H 2 O and Met, respectively. The unimolecular decompositions of the metastable and collisionally activated m/z 159 ions lead primarily to the elimination of the neutral species HNO (major) and the (Glu‒18) residue (minor). The formation of the m/z 288 ions can be described by a mechanistic scheme which involves the ion‒molecule interaction of m/z 159 with Glu and Glu–Met and subsequent losses of H 2 O and Met, respectively. Unimolecular and collisionally activated dissociations of m/z 288 suggest the formation of the proton‒bridged ion‒neutral complex [(GluNO‒18)···H + ···(Glu‒18)].

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