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Extracellular Vesicle Analysis by Paper Spray Ionization Mass Spectrometry

Paper spray ionization mass spectrometry (PSI-MS) is a direct MS analysis technique with several reported bacterial metabolomics applications. As with most MS-based bacterial studies, all currently reported PSI-MS bacterial analyses have focused on the chemical signatures of the cellular unit. One d...

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Autores principales: Chamberlain, Casey A., Hatch, Marguerite, Garrett, Timothy J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8151837/
https://www.ncbi.nlm.nih.gov/pubmed/34065030
http://dx.doi.org/10.3390/metabo11050308
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author Chamberlain, Casey A.
Hatch, Marguerite
Garrett, Timothy J.
author_facet Chamberlain, Casey A.
Hatch, Marguerite
Garrett, Timothy J.
author_sort Chamberlain, Casey A.
collection PubMed
description Paper spray ionization mass spectrometry (PSI-MS) is a direct MS analysis technique with several reported bacterial metabolomics applications. As with most MS-based bacterial studies, all currently reported PSI-MS bacterial analyses have focused on the chemical signatures of the cellular unit. One dimension of the bacterial metabolome that is often lost in such analyses is the exometabolome (extracellular metabolome), including secreted metabolites, lipids, and peptides. A key component of the bacterial exometabolome that is gaining increased attention in the microbiology and biomedical communities is extracellular vesicles (EVs). These excreted structures, produced by cells in all domains of life, contain a variety of biomolecules responsible for a wide array of cellular functions, thus representing a core component of the bacterial secreted metabolome. Although previously examined using other MS approaches, no reports currently exist for a PSI-MS analysis of bacterial EVs, nor EVs from any other organism (exosomes, ectosomes, etc.). PSI-MS holds unique analytical strengths over other commonly used MS platforms and could thus provide an advantageous approach to EV metabolomics. To address this, we report a novel application representing, to our knowledge, the first PSI-MS analysis of EVs from any organism (using the human gut resident Oxalobacter formigenes as the experimental model, a bacterium whose EVs were never previously investigated). In this report, we show how we isolated and purified EVs from bacterial culture supernatant by EV-specific affinity chromatography, confirmed and characterized these vesicles by nanoparticle tracking analysis, analyzed the EV isolate by PSI-MS, and identified a panel of EV-derived metabolites, lipids, and peptides. This work serves as a pioneering study in the field of MS-based EV analysis and provides a new, rapid, sensitive, and economical approach to EV metabolomics.
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spelling pubmed-81518372021-05-27 Extracellular Vesicle Analysis by Paper Spray Ionization Mass Spectrometry Chamberlain, Casey A. Hatch, Marguerite Garrett, Timothy J. Metabolites Communication Paper spray ionization mass spectrometry (PSI-MS) is a direct MS analysis technique with several reported bacterial metabolomics applications. As with most MS-based bacterial studies, all currently reported PSI-MS bacterial analyses have focused on the chemical signatures of the cellular unit. One dimension of the bacterial metabolome that is often lost in such analyses is the exometabolome (extracellular metabolome), including secreted metabolites, lipids, and peptides. A key component of the bacterial exometabolome that is gaining increased attention in the microbiology and biomedical communities is extracellular vesicles (EVs). These excreted structures, produced by cells in all domains of life, contain a variety of biomolecules responsible for a wide array of cellular functions, thus representing a core component of the bacterial secreted metabolome. Although previously examined using other MS approaches, no reports currently exist for a PSI-MS analysis of bacterial EVs, nor EVs from any other organism (exosomes, ectosomes, etc.). PSI-MS holds unique analytical strengths over other commonly used MS platforms and could thus provide an advantageous approach to EV metabolomics. To address this, we report a novel application representing, to our knowledge, the first PSI-MS analysis of EVs from any organism (using the human gut resident Oxalobacter formigenes as the experimental model, a bacterium whose EVs were never previously investigated). In this report, we show how we isolated and purified EVs from bacterial culture supernatant by EV-specific affinity chromatography, confirmed and characterized these vesicles by nanoparticle tracking analysis, analyzed the EV isolate by PSI-MS, and identified a panel of EV-derived metabolites, lipids, and peptides. This work serves as a pioneering study in the field of MS-based EV analysis and provides a new, rapid, sensitive, and economical approach to EV metabolomics. MDPI 2021-05-11 /pmc/articles/PMC8151837/ /pubmed/34065030 http://dx.doi.org/10.3390/metabo11050308 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Communication
Chamberlain, Casey A.
Hatch, Marguerite
Garrett, Timothy J.
Extracellular Vesicle Analysis by Paper Spray Ionization Mass Spectrometry
title Extracellular Vesicle Analysis by Paper Spray Ionization Mass Spectrometry
title_full Extracellular Vesicle Analysis by Paper Spray Ionization Mass Spectrometry
title_fullStr Extracellular Vesicle Analysis by Paper Spray Ionization Mass Spectrometry
title_full_unstemmed Extracellular Vesicle Analysis by Paper Spray Ionization Mass Spectrometry
title_short Extracellular Vesicle Analysis by Paper Spray Ionization Mass Spectrometry
title_sort extracellular vesicle analysis by paper spray ionization mass spectrometry
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8151837/
https://www.ncbi.nlm.nih.gov/pubmed/34065030
http://dx.doi.org/10.3390/metabo11050308
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