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IR action spectroscopy of glycosaminoglycan oligosaccharides

Glycosaminoglycans (GAGs) are a physio- and pharmacologically highly relevant class of complex saccharides, possessing a linear sequence and strongly acidic character. Their repetitive linear core makes them seem structurally simple at first glance, yet differences in sulfation and epimerization lea...

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Autores principales: Lettow, Maike, Grabarics, Márkó, Mucha, Eike, Thomas, Daniel A., Polewski, Łukasz, Freyse, Joanna, Rademann, Jörg, Meijer, Gerard, von Helden, Gert, Pagel, Kevin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6992547/
https://www.ncbi.nlm.nih.gov/pubmed/31853603
http://dx.doi.org/10.1007/s00216-019-02327-7
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author Lettow, Maike
Grabarics, Márkó
Mucha, Eike
Thomas, Daniel A.
Polewski, Łukasz
Freyse, Joanna
Rademann, Jörg
Meijer, Gerard
von Helden, Gert
Pagel, Kevin
author_facet Lettow, Maike
Grabarics, Márkó
Mucha, Eike
Thomas, Daniel A.
Polewski, Łukasz
Freyse, Joanna
Rademann, Jörg
Meijer, Gerard
von Helden, Gert
Pagel, Kevin
author_sort Lettow, Maike
collection PubMed
description Glycosaminoglycans (GAGs) are a physio- and pharmacologically highly relevant class of complex saccharides, possessing a linear sequence and strongly acidic character. Their repetitive linear core makes them seem structurally simple at first glance, yet differences in sulfation and epimerization lead to an enormous structural diversity with only a few GAGs having been successfully characterized to date. Recent infrared action spectroscopic experiments on sulfated mono- and disaccharide ions show great promise. Here, we assess the potential of two types of gas-phase action spectroscopy approaches in the range from 1000 to 1800 cm(−1) for the structural analysis of complex GAG oligosaccharides. Synthetic tetra- and pentasaccharides were chosen as model compounds for this benchmark study. Utilizing infrared multiple photon dissociation action spectroscopy at room temperature, diagnostic bands are largely unresolved. In contrast, cryogenic infrared action spectroscopy of ions trapped in helium nanodroplets yields resolved infrared spectra with diagnostic features for monosaccharide composition and sulfation pattern. The analysis of GAGs could therefore significantly benefit from expanding the conventional MS-based toolkit with gas-phase cryogenic IR spectroscopy. [Figure: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00216-019-02327-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-69925472020-02-11 IR action spectroscopy of glycosaminoglycan oligosaccharides Lettow, Maike Grabarics, Márkó Mucha, Eike Thomas, Daniel A. Polewski, Łukasz Freyse, Joanna Rademann, Jörg Meijer, Gerard von Helden, Gert Pagel, Kevin Anal Bioanal Chem Communication Glycosaminoglycans (GAGs) are a physio- and pharmacologically highly relevant class of complex saccharides, possessing a linear sequence and strongly acidic character. Their repetitive linear core makes them seem structurally simple at first glance, yet differences in sulfation and epimerization lead to an enormous structural diversity with only a few GAGs having been successfully characterized to date. Recent infrared action spectroscopic experiments on sulfated mono- and disaccharide ions show great promise. Here, we assess the potential of two types of gas-phase action spectroscopy approaches in the range from 1000 to 1800 cm(−1) for the structural analysis of complex GAG oligosaccharides. Synthetic tetra- and pentasaccharides were chosen as model compounds for this benchmark study. Utilizing infrared multiple photon dissociation action spectroscopy at room temperature, diagnostic bands are largely unresolved. In contrast, cryogenic infrared action spectroscopy of ions trapped in helium nanodroplets yields resolved infrared spectra with diagnostic features for monosaccharide composition and sulfation pattern. The analysis of GAGs could therefore significantly benefit from expanding the conventional MS-based toolkit with gas-phase cryogenic IR spectroscopy. [Figure: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00216-019-02327-7) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2019-12-18 2020 /pmc/articles/PMC6992547/ /pubmed/31853603 http://dx.doi.org/10.1007/s00216-019-02327-7 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Communication
Lettow, Maike
Grabarics, Márkó
Mucha, Eike
Thomas, Daniel A.
Polewski, Łukasz
Freyse, Joanna
Rademann, Jörg
Meijer, Gerard
von Helden, Gert
Pagel, Kevin
IR action spectroscopy of glycosaminoglycan oligosaccharides
title IR action spectroscopy of glycosaminoglycan oligosaccharides
title_full IR action spectroscopy of glycosaminoglycan oligosaccharides
title_fullStr IR action spectroscopy of glycosaminoglycan oligosaccharides
title_full_unstemmed IR action spectroscopy of glycosaminoglycan oligosaccharides
title_short IR action spectroscopy of glycosaminoglycan oligosaccharides
title_sort ir action spectroscopy of glycosaminoglycan oligosaccharides
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6992547/
https://www.ncbi.nlm.nih.gov/pubmed/31853603
http://dx.doi.org/10.1007/s00216-019-02327-7
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