Open AccessNegative ion tandem mass spectrometry of leukotriene E4, and LTE4, metabolites: Identification of LTE4, in human urine
Author(s) -
Angelo Sala,
Kathleen Kayganich,
Joseph A. Zirrolli,
Robert C. Murphy
Publication year - 1991
Publication title -
journal of the american society for mass spectrometry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.961
H-Index - 127
eISSN - 1879-1123
pISSN - 1044-0305
DOI - 10.1016/1044-0305(91)80023-z
Subject(s) - chemistry , tandem mass spectrometry , mass spectrometry , fast atom bombardment , chromatography , leukotriene e4 , ion , collision induced dissociation , analytical chemistry (journal) , leukotriene , organic chemistry , medicine , asthma
The sulfidopeptide leukotrienes, leukotriene E4, (LTE4,) and its N-acetyl derivative and several ω- and β-oxidized metabolites of LTE4, have been analyzed by tandem mass spectrometry. [M-H](-) ions were produced by continuous flow fast atom bombardment, and collision-induced dissociation of these ions was studied by using a triple quadrupole instrument. The product ion spectra obtained were characteristic of the structure of LTE4, and mechanisms of ion formation were investigated by using deuterated compounds. β-Elimination of the peptide portion of LTE4, by loss of CO2, and ethylene amine leaves the C-l carboxyl group ionized in the most abundant fragment ion for LTE4, and all metabolites. Tandem mass spectrometry of fast atom bombardment-generated anions from ω- and β-oxidized metabolites of LTE4, produced similar ions with only a minor influence of the third carboxyl group at the omega terminus evident. Tandem mass spectrometry was used to identify unequivocally the presence of unmodified LTE4, in a high performance liquid chromatography-purified fraction of urine from a normal healthy volunteer after infusion with LTE4.