Hyphenation of Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS) with separation methods: The art of compromises and the possible - A review.

Capillary electrophoresis (CE) Environment FT-ICR MS hyphenation Gas chromatography (GC) Liquid chromatography (LC) Omics

Journal

Talanta
ISSN: 1873-3573
Titre abrégé: Talanta
Pays: Netherlands
ID NLM: 2984816R

Informations de publication

Date de publication:
15 May 2023
Historique:
received: 28 10 2022
revised: 31 01 2023
accepted: 02 02 2023
pubmed: 14 2 2023
medline: 14 2 2023
entrez: 13 2 2023
Statut: ppublish

Résumé

This review provides an overview of the online hyphenation of Fourier Transform Ion Cyclotron Resonance Mass Spectrometry (FT-ICR MS) with separation methods to date. The online coupling between separation techniques (gas and liquid chromatography, capillary electrophoresis) and FT-ICR MS essentially raises questions of compromise and is not look as straightforward as hyphenation with other analyzers (QTOF-MS for instance). FT-ICR MS requires time to reach its highest resolving power and accuracy in mass measurement capabilities whereas chromatographic and electrophoretic peaks are transient. In many applications, the strengths and the weaknesses of each technique are balanced by their hyphenation. Untargeted "Omics" (e.g. proteomics, metabolomics, petroleomics, …) is one of the main areas of application for FT-ICR MS hyphenated to online separation techniques because of the complexity of the sample. FT-ICR MS achieves the required high mass measurement accuracy to determine accurate molecular formulae and resolution for isobar distinction. Meanwhile separation techniques highlight isomers and reduce the ion suppression effects extending the dynamic range. Even if the implementation of FT-ICR MS hyphenated with online separation methods is a little trickier (the art of compromise), this review shows that it provides unparalleled results to the scientific community (the art of the possible), along with raising the issue of its future in the field with the relentless technological progress.

Identifiants

pubmed: 36780779
pii: S0039-9140(23)00075-9
doi: 10.1016/j.talanta.2023.124324
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

124324

Informations de copyright

Copyright © 2023 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Clarisse Gosset-Erard (C)

Université de Lorraine, LCP-A2MC, F-57000, Metz, France; Laboratoire de Spectrométrie de Masse des Interactions et des Systèmes (LSMIS) UMR 7140 (Unistra-CNRS), Université de, Strasbourg, France. Electronic address: clarisse.gosset-erard@univ-lorraine.fr.

Frédéric Aubriet (F)

Université de Lorraine, LCP-A2MC, F-57000, Metz, France. Electronic address: frederic.aubriet@univ-lorraine.fr.

Emmanuelle Leize-Wagner (E)

Laboratoire de Spectrométrie de Masse des Interactions et des Systèmes (LSMIS) UMR 7140 (Unistra-CNRS), Université de, Strasbourg, France. Electronic address: leize@unistra.fr.

Yannis-Nicolas François (YN)

Laboratoire de Spectrométrie de Masse des Interactions et des Systèmes (LSMIS) UMR 7140 (Unistra-CNRS), Université de, Strasbourg, France. Electronic address: yfrancois@unistra.fr.

Patrick Chaimbault (P)

Université de Lorraine, LCP-A2MC, F-57000, Metz, France. Electronic address: patrick.chaimbault@univ-lorraine.fr.

Classifications MeSH