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      Shotgun ion mobility mass spectrometry sequencing of heparan sulfate saccharides

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          Abstract

          Despite evident regulatory roles of heparan sulfate (HS) saccharides in numerous biological processes, definitive information on the bioactive sequences of these polymers is lacking, with only a handful of natural structures sequenced to date. Here, we develop a “ Shotgun” Ion Mobility Mass Spectrometry Sequencing (SIMMS 2) method in which intact HS saccharides are dissociated in an ion mobility mass spectrometer and collision cross section values of fragments measured. Matching of data for intact and fragment ions against known values for 36 fully defined HS saccharide structures (from di- to decasaccharides) permits unambiguous sequence determination of validated standards and unknown natural saccharides, notably including variants with 3 O-sulfate groups. SIMMS 2 analysis of two fibroblast growth factor-inhibiting hexasaccharides identified from a HS oligosaccharide library screen demonstrates that the approach allows elucidation of structure-activity relationships. SIMMS 2 thus overcomes the bottleneck for decoding the informational content of functional HS motifs which is crucial for their future biomedical exploitation.

          Abstract

          Heparan sulfates (HS) contain functionally relevant structural motifs, but determining their monosaccharide sequence remains challenging. Here, the authors develop an ion mobility mass spectrometry-based method that allows unambiguous characterization of HS sequences and structure-activity relationships.

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          An Interlaboratory Evaluation of Drift Tube Ion Mobility-Mass Spectrometry Collision Cross Section Measurements.

          Collision cross section (CCS) measurements resulting from ion mobility-mass spectrometry (IM-MS) experiments provide a promising orthogonal dimension of structural information in MS-based analytical separations. As with any molecular identifier, interlaboratory standardization must precede broad range integration into analytical workflows. In this study, we present a reference drift tube ion mobility mass spectrometer (DTIM-MS) where improvements on the measurement accuracy of experimental parameters influencing IM separations provide standardized drift tube, nitrogen CCS values (DTCCSN2) for over 120 unique ion species with the lowest measurement uncertainty to date. The reproducibility of these DTCCSN2 values are evaluated across three additional laboratories on a commercially available DTIM-MS instrument. The traditional stepped field CCS method performs with a relative standard deviation (RSD) of 0.29% for all ion species across the three additional laboratories. The calibrated single field CCS method, which is compatible with a wide range of chromatographic inlet systems, performs with an average, absolute bias of 0.54% to the standardized stepped field DTCCSN2 values on the reference system. The low RSD and biases observed in this interlaboratory study illustrate the potential of DTIM-MS for providing a molecular identifier for a broad range of discovery based analyses.
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            Recommendations for reporting ion mobility Mass Spectrometry measurements

            Here we present a guide to ion mobility mass spectrometry experiments, which covers both linear and nonlinear methods: what is measured, how the measurements are done, and how to report the results, including the uncertainties of mobility and collision cross section values. The guide aims to clarify some possibly confusing concepts, and the reporting recommendations should help researchers, authors and reviewers to contribute comprehensive reports, so that the ion mobility data can be reused more confidently. Starting from the concept of the definition of the measurand, we emphasize that (i) mobility values (K 0) depend intrinsically on ion structure, the nature of the bath gas, temperature, and E/N; (ii) ion mobility does not measure molecular surfaces directly, but collision cross section (CCS) values are derived from mobility values using a physical model; (iii) methods relying on calibration are empirical (and thus may provide method‐dependent results) only if the gas nature, temperature or E/N cannot match those of the primary method. Our analysis highlights the urgency of a community effort toward establishing primary standards and reference materials for ion mobility, and provides recommendations to do so. © 2019 The Authors. Mass Spectrometry Reviews Published by Wiley Periodicals, Inc.
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              Identification of carbohydrate anomers using ion mobility-mass spectrometry.

              Carbohydrates are ubiquitous biological polymers that are important in a broad range of biological processes. However, owing to their branched structures and the presence of stereogenic centres at each glycosidic linkage between monomers, carbohydrates are harder to characterize than are peptides and oligonucleotides. Methods such as nuclear magnetic resonance spectroscopy can be used to characterize glycosidic linkages, but this technique requires milligram amounts of material and cannot detect small amounts of coexisting isomers. Mass spectrometry, on the other hand, can provide information on carbohydrate composition and connectivity for even small amounts of sample, but it cannot be used to distinguish between stereoisomers. Here, we demonstrate that ion mobility-mass spectrometry--a method that separates molecules according to their mass, charge, size, and shape--can unambiguously identify carbohydrate linkage-isomers and stereoisomers. We analysed six synthetic carbohydrate isomers that differ in composition, connectivity, or configuration. Our data show that coexisting carbohydrate isomers can be identified, and relative concentrations of the minor isomer as low as 0.1 per cent can be detected. In addition, the analysis is rapid, and requires no derivatization and only small amounts of sample. These results indicate that ion mobility-mass spectrometry is an effective tool for the analysis of complex carbohydrates. This method could have an impact on the field of carbohydrate synthesis similar to that of the advent of high-performance liquid chromatography on the field of peptide assembly in the late 1970s.
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                Author and article information

                Contributors
                rmiller@sund.ku.dk
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                20 March 2020
                20 March 2020
                2020
                : 11
                : 1481
                Affiliations
                [1 ]ISNI 0000 0001 0674 042X, GRID grid.5254.6, Copenhagen Center for Glycomics, Department of Cellular & Molecular Medicine, , University of Copenhagen, ; Copenhagen, N 2200 Denmark
                [2 ]ISNI 0000 0004 1936 8470, GRID grid.10025.36, Centre for Glycobiology, Department of Biochemistry, Institute of Integrative Biology, , University of Liverpool, ; Crown Street, Liverpool, L69 7ZB UK
                [3 ]ISNI 0000 0004 1936 8948, GRID grid.4991.5, Laboratory of Cancer Biology, Department of Oncology, Medical Sciences Division, , University of Oxford, Old Road Campus Research Building, ; Old Road Campus, Roosevelt Drive, Oxford, OX3 7DQ UK
                [4 ]ISNI 0000 0004 0415 6205, GRID grid.9757.c, Institute for Science and Technology in Medicine, School of Medicine, , Keele University, ; Keele, Staffordshire ST5 5BG UK
                [5 ]ISNI 0000 0001 2292 3111, GRID grid.267827.e, Ferrier Research Institute, Victoria University of Wellington, 69 Gracefield Road, Gracefield, ; Lower Hutt, 5010 New Zealand
                [6 ]ISNI 0000 0001 1034 1720, GRID grid.410711.2, Division of Chemical Biology and Medicinal Chemistry, Eshelman School of Pharmacy, , University of North Carolina, ; Chapel Hill, NC 27599 USA
                [7 ]ISNI 0000 0004 1936 738X, GRID grid.213876.9, Complex Carbohydrate Research Center, , University of Georgia, ; 315 Riverbend Road, Athens, GA 30602 USA
                [8 ]ISNI 0000000120346234, GRID grid.5477.1, Department of Chemical Biology and Drug Discovery, Utrecht Institute for Pharmaceutical Science, and Bijvoet Center for Biomolecular Research, , Utrecht University, ; Universiteitsweg 99, 3584 CG Utrecht, The Netherlands
                [9 ]ISNI 0000 0000 9116 4836, GRID grid.14095.39, Freie Universitaet Berlin, Institute of Chemistry and Biochemistry, ; Takustrasse 3, 14195 Berlin, Germany
                [10 ]ISNI 0000 0001 0565 1775, GRID grid.418028.7, Fritz Haber Institute of the Max Planck Society, ; Faradayweg 4-6, 14195 Berlin, Germany
                [11 ]ISNI 0000 0000 9919 9582, GRID grid.8761.8, Department of Medical Biochemistry and Cell Biology, Institute of Biomedicine, Sahlgrenska Academy, , University of Gothenburg, ; Gothenburg, Sweden
                [12 ]ISNI 0000 0004 1936 8948, GRID grid.4991.5, Department of Chemistry, Chemistry Research Laboratory, , University of Oxford, ; Oxford, OX1 3QZ UK
                Author information
                http://orcid.org/0000-0001-8574-1948
                http://orcid.org/0000-0002-9352-6559
                http://orcid.org/0000-0002-6892-8812
                http://orcid.org/0000-0002-3151-6208
                http://orcid.org/0000-0002-6003-4574
                http://orcid.org/0000-0003-3111-5954
                http://orcid.org/0000-0002-2550-637X
                http://orcid.org/0000-0003-2975-5450
                http://orcid.org/0000-0002-3045-2628
                http://orcid.org/0000-0001-8054-4718
                Article
                15284
                10.1038/s41467-020-15284-y
                7083916
                32198425
                69539108-91a4-4994-8df9-2c8c646452a4
                © The Author(s) 2020

                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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 2 September 2019
                : 27 February 2020
                Funding
                Funded by: FundRef https://doi.org/10.13039/501100000289, Cancer Research UK (CRUK);
                Award ID: CRUK0317
                Award Recipient :
                Funded by: FundRef https://doi.org/10.13039/501100001732, Danmarks Grundforskningsfond (Danish National Research Foundation);
                Award ID: DNFR107
                Award Recipient :
                Funded by: FundRef https://doi.org/10.13039/100000009, Foundation for the National Institutes of Health (Foundation for the National Institutes of Health, Inc.);
                Award ID: HL094463-09
                Award ID: HL144970
                Award ID: NIGMS; P41GM103390
                Award ID: P41 RR005351
                Award Recipient :
                Funded by: FundRef https://doi.org/10.13039/501100000854, Human Frontier Science Program (HFSP);
                Award ID: RGP0062
                Award ID: RGP0062
                Award Recipient :
                Funded by: FundRef https://doi.org/10.13039/501100000265, RCUK | Medical Research Council (MRC);
                Award ID: G117/423
                Award Recipient :
                Funded by: FundRef https://doi.org/10.13039/501100000268, RCUK | Biotechnology and Biological Sciences Research Council (BBSRC);
                Award ID: BB/I004343/1; BB/K02128/1; BB/MO27791
                Award Recipient :
                Funded by: FundRef https://doi.org/10.13039/501100009187, RCUK | MRC | Medical Research Foundation;
                Award ID: PhD studentship
                Award Recipient :
                Funded by: FundRef https://doi.org/10.13039/501100001659, Deutsche Forschungsgemeinschaft (German Research Foundation);
                Award ID: 372486779 – SFB 1340
                Award Recipient :
                Categories
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                © The Author(s) 2020

                Uncategorized
                carbohydrates,glycobiology,mass spectrometry
                Uncategorized
                carbohydrates, glycobiology, mass spectrometry

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