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Ion-Pairing Chromatography and Amine Derivatization Provide Complementary Approaches for the Targeted LC-MS Analysis of the Polar Metabolome

[Image: see text] Liquid chromatography coupled to mass spectrometry is a key metabolomics/metabonomics technology. Reversed-phase liquid chromatography (RPLC) is very widely used as a separation step, but typically has poor retention of highly polar metabolites. Here, we evaluated the combination o...

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Autores principales: Sagi-Kiss, Virag, Li, Yufeng, Carey, Matthew R., Grover, Sarah J., Siems, Karsten, Cirulli, Francesca, Berry, Alessandra, Musillo, Chiara, Wilson, Ian D., Want, Elizabeth J., Bundy, Jacob G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9171846/
https://www.ncbi.nlm.nih.gov/pubmed/35536659
http://dx.doi.org/10.1021/acs.jproteome.2c00030
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author Sagi-Kiss, Virag
Li, Yufeng
Carey, Matthew R.
Grover, Sarah J.
Siems, Karsten
Cirulli, Francesca
Berry, Alessandra
Musillo, Chiara
Wilson, Ian D.
Want, Elizabeth J.
Bundy, Jacob G.
author_facet Sagi-Kiss, Virag
Li, Yufeng
Carey, Matthew R.
Grover, Sarah J.
Siems, Karsten
Cirulli, Francesca
Berry, Alessandra
Musillo, Chiara
Wilson, Ian D.
Want, Elizabeth J.
Bundy, Jacob G.
author_sort Sagi-Kiss, Virag
collection PubMed
description [Image: see text] Liquid chromatography coupled to mass spectrometry is a key metabolomics/metabonomics technology. Reversed-phase liquid chromatography (RPLC) is very widely used as a separation step, but typically has poor retention of highly polar metabolites. Here, we evaluated the combination of two alternative methods for improving retention of polar metabolites based on 6-aminoquinoloyl-N-hydroxysuccinidimyl carbamate derivatization for amine groups, and ion-pairing chromatography (IPC) using tributylamine as an ion-pairing agent to retain acids. We compared both of these methods to RPLC and also to each other, for targeted analysis using a triple-quadrupole mass spectrometer, applied to a library of ca. 500 polar metabolites. IPC and derivatization were complementary in terms of their coverage: combined, they improved the proportion of metabolites with good retention to 91%, compared to just 39% for RPLC alone. The combined method was assessed by analyzing a set of liver extracts from aged male and female mice that had been treated with the polyphenol compound ampelopsin. Not only were a number of significantly changed metabolites detected, but also it could be shown that there was a clear interaction between ampelopsin treatment and sex, in that the direction of metabolite change was opposite for males and females.
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spelling pubmed-91718462022-06-08 Ion-Pairing Chromatography and Amine Derivatization Provide Complementary Approaches for the Targeted LC-MS Analysis of the Polar Metabolome Sagi-Kiss, Virag Li, Yufeng Carey, Matthew R. Grover, Sarah J. Siems, Karsten Cirulli, Francesca Berry, Alessandra Musillo, Chiara Wilson, Ian D. Want, Elizabeth J. Bundy, Jacob G. J Proteome Res [Image: see text] Liquid chromatography coupled to mass spectrometry is a key metabolomics/metabonomics technology. Reversed-phase liquid chromatography (RPLC) is very widely used as a separation step, but typically has poor retention of highly polar metabolites. Here, we evaluated the combination of two alternative methods for improving retention of polar metabolites based on 6-aminoquinoloyl-N-hydroxysuccinidimyl carbamate derivatization for amine groups, and ion-pairing chromatography (IPC) using tributylamine as an ion-pairing agent to retain acids. We compared both of these methods to RPLC and also to each other, for targeted analysis using a triple-quadrupole mass spectrometer, applied to a library of ca. 500 polar metabolites. IPC and derivatization were complementary in terms of their coverage: combined, they improved the proportion of metabolites with good retention to 91%, compared to just 39% for RPLC alone. The combined method was assessed by analyzing a set of liver extracts from aged male and female mice that had been treated with the polyphenol compound ampelopsin. Not only were a number of significantly changed metabolites detected, but also it could be shown that there was a clear interaction between ampelopsin treatment and sex, in that the direction of metabolite change was opposite for males and females. American Chemical Society 2022-05-10 2022-06-03 /pmc/articles/PMC9171846/ /pubmed/35536659 http://dx.doi.org/10.1021/acs.jproteome.2c00030 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Sagi-Kiss, Virag
Li, Yufeng
Carey, Matthew R.
Grover, Sarah J.
Siems, Karsten
Cirulli, Francesca
Berry, Alessandra
Musillo, Chiara
Wilson, Ian D.
Want, Elizabeth J.
Bundy, Jacob G.
Ion-Pairing Chromatography and Amine Derivatization Provide Complementary Approaches for the Targeted LC-MS Analysis of the Polar Metabolome
title Ion-Pairing Chromatography and Amine Derivatization Provide Complementary Approaches for the Targeted LC-MS Analysis of the Polar Metabolome
title_full Ion-Pairing Chromatography and Amine Derivatization Provide Complementary Approaches for the Targeted LC-MS Analysis of the Polar Metabolome
title_fullStr Ion-Pairing Chromatography and Amine Derivatization Provide Complementary Approaches for the Targeted LC-MS Analysis of the Polar Metabolome
title_full_unstemmed Ion-Pairing Chromatography and Amine Derivatization Provide Complementary Approaches for the Targeted LC-MS Analysis of the Polar Metabolome
title_short Ion-Pairing Chromatography and Amine Derivatization Provide Complementary Approaches for the Targeted LC-MS Analysis of the Polar Metabolome
title_sort ion-pairing chromatography and amine derivatization provide complementary approaches for the targeted lc-ms analysis of the polar metabolome
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9171846/
https://www.ncbi.nlm.nih.gov/pubmed/35536659
http://dx.doi.org/10.1021/acs.jproteome.2c00030
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