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Stable Isotope Phosphate Labelling of Diverse Metabolites is Enabled by a Family of (18)O‐Phosphoramidites

Stable isotope labelling is state‐of‐the‐art in quantitative mass spectrometry, yet often accessing the required standards is cumbersome and very expensive. Here, a unifying synthetic concept for (18)O‐labelled phosphates is presented, based on a family of modified (18)O(2)‐phosphoramidite reagents....

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Detalles Bibliográficos
Autores principales: Haas, Thomas M., Mundinger, Stephan, Qiu, Danye, Jork, Nikolaus, Ritter, Kevin, Dürr‐Mayer, Tobias, Ripp, Alexander, Saiardi, Adolfo, Schaaf, Gabriel, Jessen, Henning J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9298905/
https://www.ncbi.nlm.nih.gov/pubmed/34734451
http://dx.doi.org/10.1002/anie.202112457
Descripción
Sumario:Stable isotope labelling is state‐of‐the‐art in quantitative mass spectrometry, yet often accessing the required standards is cumbersome and very expensive. Here, a unifying synthetic concept for (18)O‐labelled phosphates is presented, based on a family of modified (18)O(2)‐phosphoramidite reagents. This toolbox offers access to major classes of biologically highly relevant phosphorylated metabolites as their isotopologues including nucleotides, inositol phosphates, ‐pyrophosphates, and inorganic polyphosphates. (18)O‐enrichment ratios >95 % and good yields are obtained consistently in gram‐scale reactions, while enabling late‐stage labelling. We demonstrate the utility of the (18)O‐labelled inositol phosphates and pyrophosphates by assignment of these metabolites from different biological matrices. We demonstrate that phosphate neutral loss is negligible in an analytical setup employing capillary electrophoresis electrospray ionisation triple quadrupole mass spectrometry.