Literature DB >> 3395713

Characterization of glutathione conjugates by fast atom bombardment/tandem mass spectrometry.

P E Haroldsen1, M H Reilly, H Hughes, S J Gaskell, C J Porter.   

Abstract

The collisionally activated decomposition of [M + H]+ ions, generated by fast atom bombardment (FAB) of glutathione conjugates, has been studied by tandem mass spectrometry (MS/MS) using hybrid sector/quadrupole instruments. Abundant fragments of diagnostic utility were present in the daughter ion spectra. Common fragmentation modes were observed but their relative importance was strongly dependent on the nature of the conjugated species. As an example of a general approach to the characterization of glutathione conjugates in biological samples, the acetaminophen-glutathione conjugate was identified in rat bile, following coadministration of (2H0)- and (2H3)acetaminophen, using the experimental sequence: (i) conventional FAB mass spectrometric analysis, (ii) MS/MS using constant neutral loss (129 u) scanning to identify parent ions corresponding to glutathione conjugates, (iii) MS/MS to yield daughter ion spectra of parents so identified and corresponding to (2H0)- and (2H3)-labeled conjugates.

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Year:  1988        PMID: 3395713     DOI: 10.1002/bms.1200151107

Source DB:  PubMed          Journal:  Biomed Environ Mass Spectrom        ISSN: 0887-6134


  7 in total

1.  Selective Gas-Phase Ion/Ion Reactions: Enabling Disulfide Mapping via Oxidation and Cleavage of Disulfide Bonds in Intermolecularly-Linked Polypeptide Ions.

Authors:  Alice L Pilo; Scott A McLuckey
Journal:  Anal Chem       Date:  2016-08-29       Impact factor: 6.986

2.  Detection of reactive metabolites using isotope-labeled glutathione trapping and simultaneous neutral loss and precursor ion scanning with ultra-high-pressure liquid chromatography triple quadruple mass spectrometry.

Authors:  Ke Huang; Lingyi Huang; Richard B van Breemen
Journal:  Anal Chem       Date:  2015-03-25       Impact factor: 6.986

3.  Fragmentation characteristic of glutathione conjugates activated by high-energy collisions.

Authors:  C M Murphy; C Fenselau; P L Gutierrez
Journal:  J Am Soc Mass Spectrom       Date:  1992-11       Impact factor: 3.109

4.  Mass spectrometric methods for distinguishing structural isomers of glutathione conjugates of estrone and estradiol.

Authors:  R Ramanathan; K Cao; E Cavalieri; M L Gross
Journal:  J Am Soc Mass Spectrom       Date:  1998-06       Impact factor: 3.109

5.  Nucleophile addition of reduced glutathione on 2-methyl-2-nitroso compound: a combined electron paramagnetic resonance spectroscopy and electrospray tandem mass spectrometry study.

Authors:  Mathilde Triquigneaux; Béatrice Tuccio; Robert Lauricella; Laurence Charles
Journal:  J Am Soc Mass Spectrom       Date:  2009-08-07       Impact factor: 3.109

6.  Multiple scan modes in the hybrid tandem mass spectrometric screening and characterization of the glutathione conjugate of 2-furamide.

Authors:  K D Ballard; M J Raftery; H Jaeschke; S J Gaskell
Journal:  J Am Soc Mass Spectrom       Date:  1991-01       Impact factor: 3.109

7.  Role of Glutathione Conjugation in 1-Bromobutane-induced Immunotoxicity in Mice.

Authors:  Sang Kyu Lee; Dong Ju Lee; Tae Won Jeon; Gyu Sub Ko; Se Hyun Yoo; Hyun Woo Ha; Mi Jeong Kang; Wonku Kang; Sang Kyum Kim; Tae Cheon Jeong
Journal:  Toxicol Res       Date:  2010-06
  7 in total

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