The rapid separation and characterization of sulfates of tyrosine and its metabolites in reaction mixtures and human urine using a cyclic ion mobility device and mass spectrometry.

Human urine Ion mobility separations Reaction mixtures Tyrosine sulfates

Journal

Journal of chromatography. A
ISSN: 1873-3778
Titre abrégé: J Chromatogr A
Pays: Netherlands
ID NLM: 9318488

Informations de publication

Date de publication:
20 Dec 2023
Historique:
received: 27 09 2023
revised: 13 12 2023
accepted: 19 12 2023
medline: 7 1 2024
pubmed: 7 1 2024
entrez: 6 1 2024
Statut: aheadofprint

Résumé

Ion mobility (IM) separations, especially when combined with mass spectrometry, offer the opportunity for the rapid analysis and characterization of mixtures. However, the limited resolution afforded by many IM systems means that in practice applications may be limited. Here we have employed an IM separation on a high-resolution cyclic IM device with MS/MS to separate and characterize mixtures of sulfated isomers of tyrosine and associated metabolites containing multiple sulfated isoforms present in reaction mixtures. The cIMS device allowed ions, not resolved using a single pass, to be subjected to multiple passes, enabling the resolution of those with similar collision cross sections (CCS). Predicted single pass CCS values calculated for the isomers likely to be present in these mixtures showed only small differences between them, ranging between of between 0.1 - 0.7 % depending on structure. These small differences highlight the high degree of mobility resolution required for separating the isomers. Experimentally different isoforms of tyrosine sulfate and sulfated tyrosine metabolites could be sufficiently resolved via multipass separations (3-35 passes). This degree of separation provided resolving powers of up to 384 CCS/ΔCCS for sulfated dopamine which enabled good MS/MS spectra to be generated. In human urine the presence of a single sulfated form of tyrosine was detected and identified as the O-sulfate after 3 passes based on the synthetic standard. Of the other tyrosine-related sulfates for which synthetic standards had been prepared only dopamine sulfate was detected in this sample.

Identifiants

pubmed: 38183784
pii: S0021-9673(23)00822-1
doi: 10.1016/j.chroma.2023.464597
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

464597

Informations de copyright

Copyright © 2023. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: ID Wilson reports financial support was provided by Waters Corporation.

Auteurs

Adam M King (AM)

Waters Corporation, Wilmslow, Cheshire, SK9 4AX, UK; Medical and Molecular and Forensic Sciences, Murdoch University, South Street, Murdoch, WA 6150, Australia. Electronic address: adam_king@waters.com.

Ian D Wilson (ID)

Computational and Systems Medicine, Department of Metabolism, Digestion and Reproduction, Imperial College, Burlington Danes Building, Du Cane Road, London, W12 0NN, UK. Electronic address: i.wilson@imperial.ac.uk.

Robert S Plumb (RS)

Medical and Molecular and Forensic Sciences, Murdoch University, South Street, Murdoch, WA 6150, Australia; Waters Corporation, Milford, MA, 01757, USA.

Lee A Gethings (LA)

Waters Corporation, Wilmslow, Cheshire, SK9 4AX, UK; School of Biological Sciences, Division of Infection, Immunity and Respiratory Medicine, University of Manchester, Manchester, UK; Faculty of Health & Medical Sciences, University of Surrey, Guildford, UK.

Robert Trengove (R)

CHIRI, Curtin University, Kent St, Bentley, WA, 6102, Australia.

Garth Maker (G)

Medical and Molecular and Forensic Sciences, Murdoch University, South Street, Murdoch, WA 6150, Australia.

Classifications MeSH