Effects of Different Adduct Ions, Ionization Temperatures, and Solvents on the Ion Mobility of Glycans

The structural analysis of glycans remains a major challenge due to their high isomeric complexity and conformational flexibility arising from diverse glycosidic linkages and dynamic three-dimensional structures. Ion mobility–mass spectrometry (IM–MS) has been attracting attention as a way to develo...

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Published inMolecules (Basel, Switzerland) Vol. 30; no. 10; p. 2177
Main Authors Feng, Hao, Yamaguchi, Takumi
Format Journal Article
LanguageEnglish
Published Switzerland MDPI AG 15.05.2025
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Abstract The structural analysis of glycans remains a major challenge due to their high isomeric complexity and conformational flexibility arising from diverse glycosidic linkages and dynamic three-dimensional structures. Ion mobility–mass spectrometry (IM–MS) has been attracting attention as a way to develop the structural analysis of glycans. In this study, the effects of ionization conditions—including different types of adduct ions, ionization temperatures, and solvent environments—on the ion mobility behavior of glycans were systematically investigated. IM–MS measurements of ethylamine-tagged glycans showed broad arrival time distributions of monoprotonated ions indicating the presence of multiple conformers of glycans. Increased ionization temperatures and the use of methanol as a solvent further broadened the distribution, suggesting the enhanced conformational dynamics of the glycan ions. In contrast, sodium adduct ions yielded narrower distributions, implying that the interactions between sodium ions and glycans constrained structural flexibility. These results demonstrate that ionization parameters have a significant impact on glycan conformational behavior and mobility in the gas phase. This study provides insights into the analytical conditions for IM–MS measurements of glycans and highlights the utility of this method as a powerful tool for elucidating glycan structure and dynamics.
AbstractList The structural analysis of glycans remains a major challenge due to their high isomeric complexity and conformational flexibility arising from diverse glycosidic linkages and dynamic three-dimensional structures. Ion mobility–mass spectrometry (IM–MS) has been attracting attention as a way to develop the structural analysis of glycans. In this study, the effects of ionization conditions—including different types of adduct ions, ionization temperatures, and solvent environments—on the ion mobility behavior of glycans were systematically investigated. IM–MS measurements of ethylamine-tagged glycans showed broad arrival time distributions of monoprotonated ions indicating the presence of multiple conformers of glycans. Increased ionization temperatures and the use of methanol as a solvent further broadened the distribution, suggesting the enhanced conformational dynamics of the glycan ions. In contrast, sodium adduct ions yielded narrower distributions, implying that the interactions between sodium ions and glycans constrained structural flexibility. These results demonstrate that ionization parameters have a significant impact on glycan conformational behavior and mobility in the gas phase. This study provides insights into the analytical conditions for IM–MS measurements of glycans and highlights the utility of this method as a powerful tool for elucidating glycan structure and dynamics.
The structural analysis of glycans remains a major challenge due to their high isomeric complexity and conformational flexibility arising from diverse glycosidic linkages and dynamic three-dimensional structures. Ion mobility-mass spectrometry (IM-MS) has been attracting attention as a way to develop the structural analysis of glycans. In this study, the effects of ionization conditions-including different types of adduct ions, ionization temperatures, and solvent environments-on the ion mobility behavior of glycans were systematically investigated. IM-MS measurements of ethylamine-tagged glycans showed broad arrival time distributions of monoprotonated ions indicating the presence of multiple conformers of glycans. Increased ionization temperatures and the use of methanol as a solvent further broadened the distribution, suggesting the enhanced conformational dynamics of the glycan ions. In contrast, sodium adduct ions yielded narrower distributions, implying that the interactions between sodium ions and glycans constrained structural flexibility. These results demonstrate that ionization parameters have a significant impact on glycan conformational behavior and mobility in the gas phase. This study provides insights into the analytical conditions for IM-MS measurements of glycans and highlights the utility of this method as a powerful tool for elucidating glycan structure and dynamics.The structural analysis of glycans remains a major challenge due to their high isomeric complexity and conformational flexibility arising from diverse glycosidic linkages and dynamic three-dimensional structures. Ion mobility-mass spectrometry (IM-MS) has been attracting attention as a way to develop the structural analysis of glycans. In this study, the effects of ionization conditions-including different types of adduct ions, ionization temperatures, and solvent environments-on the ion mobility behavior of glycans were systematically investigated. IM-MS measurements of ethylamine-tagged glycans showed broad arrival time distributions of monoprotonated ions indicating the presence of multiple conformers of glycans. Increased ionization temperatures and the use of methanol as a solvent further broadened the distribution, suggesting the enhanced conformational dynamics of the glycan ions. In contrast, sodium adduct ions yielded narrower distributions, implying that the interactions between sodium ions and glycans constrained structural flexibility. These results demonstrate that ionization parameters have a significant impact on glycan conformational behavior and mobility in the gas phase. This study provides insights into the analytical conditions for IM-MS measurements of glycans and highlights the utility of this method as a powerful tool for elucidating glycan structure and dynamics.
Audience Academic
Author Yamaguchi, Takumi
Feng, Hao
AuthorAffiliation 2 Graduate School of Pharmaceutical Sciences, Nagoya City University, 3-1 Tanabe-dori, Mizuho-ku, Nagoya 4678603, Japan
3 Exploratory Research Center on Life and Living Systems (ExCELLS), National Institutes of Natural Sciences, 5-1 Higashiyama, Myodaiji, Okazaki 4448787, Japan
1 School of Materials Science, Japan Advanced Institute of Science and Technology, 1-1 Asahidai, Nomi 9231292, Japan
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Cites_doi 10.1016/j.chembiol.2013.12.010
10.1007/s10719-015-9613-7
10.1039/C5CP06288H
10.1021/ac8016295
10.1016/j.bbagen.2016.02.003
10.4052/tigg.2013.2E
10.1038/nature15388
10.1007/s10719-019-09876-0
10.1038/nchem.1889
10.1039/D2CP05203B
10.1021/jacs.5b01338
10.1021/cr990302n
10.1021/acs.analchem.9b01772
10.1021/ac504720m
10.1038/s41598-018-20012-0
10.1021/acs.chemrev.2c00600
10.1021/ac201509p
10.1093/glycob/cww086
10.1021/jacsau.3c00639
10.1021/acs.analchem.6b04998
10.1016/S1387-3806(98)14135-0
10.1016/j.pnmrs.2024.10.002
10.1021/jacs.9b06406
10.1021/cr940283b
10.1002/(SICI)1096-9888(199605)31:5<445::AID-JMS354>3.0.CO;2-G
10.1021/jasms.2c00165
10.1016/j.ijms.2003.10.010
10.1255/ejms.947
10.1007/s10719-012-9376-3
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Keywords ion mobility spectrometry
mass spectrometry
glycans
electrospray ionization
conformational dynamics
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References Morsa (ref_28) 2011; 83
Gray (ref_18) 2017; 89
Angulo (ref_9) 2024; 144–145
Struwe (ref_20) 2016; 33
Karch (ref_22) 2021; 121
Widmalm (ref_8) 2024; 4
Harvey (ref_16) 2012; 26
Christofi (ref_21) 2023; 123
Harvey (ref_25) 2016; 30
Ruda (ref_11) 2023; 25
Hinneburg (ref_24) 2020; 26
Warnke (ref_30) 2015; 137
Shvartsburg (ref_35) 2008; 80
Cummings (ref_2) 2019; 36
Dwek (ref_4) 1996; 96
Lanucara (ref_15) 2014; 6
Chung (ref_31) 2023; 34
Li (ref_32) 1999; 185–187
Varki (ref_1) 2017; 27
Jin (ref_13) 2019; 91
Cummings (ref_3) 2014; 21
Gray (ref_5) 2019; 141
Gray (ref_12) 2016; 1860
Smith (ref_27) 2009; 15
Duus (ref_7) 2000; 100
ref_23
May (ref_14) 2015; 87
Wuhrer (ref_6) 2013; 30
ref_29
(ref_33) 1996; 31
Manabe (ref_19) 2022; 33
Hofmann (ref_17) 2015; 526
Yamaguchi (ref_10) 2020; 32
Pendrill (ref_34) 2016; 18
Gabelica (ref_26) 2004; 231
References_xml – volume: 26
  start-page: 175
  year: 2012
  ident: ref_16
  article-title: Confident Identification of Isomeric N-Glycan Structures by Combined Ion Mobility Mass Spectrometry and Hydrophilic Interaction Liquid Chromatography
  publication-title: Rapid Commun. Mass Spectrom.
– volume: 21
  start-page: 1
  year: 2014
  ident: ref_3
  article-title: The Challenge and Promise of Glycomics
  publication-title: Chem. Biol.
  doi: 10.1016/j.chembiol.2013.12.010
– volume: 33
  start-page: 399
  year: 2016
  ident: ref_20
  article-title: GlycoMob: An Ion Mobility-Mass Spectrometry Collision Cross Section Database for Glycomics
  publication-title: Glycoconj. J.
  doi: 10.1007/s10719-015-9613-7
– volume: 18
  start-page: 3086
  year: 2016
  ident: ref_34
  article-title: Flexibility at a Glycosidic Linkage Revealed by Molecular Dynamics, Stochastic Modeling, and 13C NMR Spin Relaxation: Conformational Preferences of α-L-Rhap-α-(1→2)-α-L-Rhap-OMe in Water and Dimethyl Sulfoxide Solutions
  publication-title: Phys. Chem. Chem. Phys.
  doi: 10.1039/C5CP06288H
– volume: 80
  start-page: 9689
  year: 2008
  ident: ref_35
  article-title: Fundamentals of Traveling Wave Ion Mobility Spectrometry
  publication-title: Anal. Chem.
  doi: 10.1021/ac8016295
– volume: 1860
  start-page: 1688
  year: 2016
  ident: ref_12
  article-title: Applications of Ion Mobility Mass Spectrometry for High Throughput, High Resolution Glycan Analysis
  publication-title: Biochim. Biophys. Acta
  doi: 10.1016/j.bbagen.2016.02.003
– volume: 32
  start-page: E93
  year: 2020
  ident: ref_10
  article-title: Delineating the Dynamic Conformations of Oligosaccharides by Combining Molecular Simulation and NMR Spectroscopy
  publication-title: Trends Glycosci. Glycotechnol.
  doi: 10.4052/tigg.2013.2E
– volume: 526
  start-page: 241
  year: 2015
  ident: ref_17
  article-title: Identification of Carbohydrate Anomers Using Ion Mobility–Mass Spectrometry
  publication-title: Nature
  doi: 10.1038/nature15388
– volume: 36
  start-page: 241
  year: 2019
  ident: ref_2
  article-title: Stuck on Sugars—How Carbohydrates Regulate Cell Adhesion, Recognition, and Signaling
  publication-title: Glycoconj. J.
  doi: 10.1007/s10719-019-09876-0
– volume: 121
  start-page: 806
  year: 2021
  ident: ref_22
  article-title: High-Resolution Native Mass Spectrometry
  publication-title: Chem. Rev.
– volume: 34
  start-page: 234
  year: 2023
  ident: ref_31
  article-title: Solvent Composition Can Have a Measurable Influence on the Ion Mobility-Derived Collision Cross Section of Small Molecules
  publication-title: J. Am. Soc. Mass Spectrom.
– volume: 6
  start-page: 281
  year: 2014
  ident: ref_15
  article-title: The Power of Ion Mobility-Mass Spectrometry for Structural Characterization and the Study of Conformational Dynamics
  publication-title: Nat. Chem.
  doi: 10.1038/nchem.1889
– volume: 25
  start-page: 3042
  year: 2023
  ident: ref_11
  article-title: Glycosidic α-Linked Mannopyranose Disaccharides: An NMR Spectroscopy and Molecular Dynamics Simulation Study Employing Additive and Drude Polarizable Force Fields
  publication-title: Phys. Chem. Chem. Phys.
  doi: 10.1039/D2CP05203B
– volume: 26
  start-page: 12213
  year: 2020
  ident: ref_24
  article-title: Identification of Isomeric N-Glycans by Conformer Distribution Fingerprinting Using Ion Mobility Mass Spectrometry
  publication-title: Chem. Eur. J.
– volume: 137
  start-page: 4236
  year: 2015
  ident: ref_30
  article-title: Protomers of Benzocaine: Solvent and Permittivity Dependence
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.5b01338
– volume: 100
  start-page: 4589
  year: 2000
  ident: ref_7
  article-title: Carbohydrate Structural Determination by NMR Spectroscopy: Modern Methods and Limitations
  publication-title: Chem. Rev.
  doi: 10.1021/cr990302n
– volume: 91
  start-page: 10604
  year: 2019
  ident: ref_13
  article-title: Separation of Isomeric O-Glycans by Ion Mobility and Liquid Chromatography–Mass Spectrometry
  publication-title: Anal. Chem.
  doi: 10.1021/acs.analchem.9b01772
– volume: 87
  start-page: 1422
  year: 2015
  ident: ref_14
  article-title: Ion Mobility-Mass Spectrometry: Time-Dispersive Instrumentation
  publication-title: Anal. Chem.
  doi: 10.1021/ac504720m
– ident: ref_23
  doi: 10.1038/s41598-018-20012-0
– volume: 123
  start-page: 2902
  year: 2023
  ident: ref_21
  article-title: Ion Mobility Mass Spectrometry (IM-MS) for Structural Biology: Insights Gained by Measuring Mass, Charge, and Collision Cross Section
  publication-title: Chem. Rev.
  doi: 10.1021/acs.chemrev.2c00600
– volume: 83
  start-page: 5775
  year: 2011
  ident: ref_28
  article-title: Effective Temperature of Ions in Traveling Wave Ion Mobility Spectrometry
  publication-title: Anal. Chem.
  doi: 10.1021/ac201509p
– ident: ref_29
– volume: 27
  start-page: 3
  year: 2017
  ident: ref_1
  article-title: Biological Roles of Glycans
  publication-title: Glycobiology
  doi: 10.1093/glycob/cww086
– volume: 4
  start-page: 20
  year: 2024
  ident: ref_8
  article-title: Glycan Shape, Motions, and Interactions Explored by NMR Spectroscopy
  publication-title: JACS Au
  doi: 10.1021/jacsau.3c00639
– volume: 89
  start-page: 4540
  year: 2017
  ident: ref_18
  article-title: Bottom-Up Elucidation of Glycosidic Bond Stereochemistry
  publication-title: Anal. Chem.
  doi: 10.1021/acs.analchem.6b04998
– volume: 30
  start-page: 235
  year: 2016
  ident: ref_25
  article-title: Travelling-Wave Ion Mobility and Negative Ion Fragmentation of High Mannose N-Glycans
  publication-title: Rapid Commun. Mass Spectrom.
– volume: 185–187
  start-page: 37
  year: 1999
  ident: ref_32
  article-title: Influence of Solvent Composition and Capillary Temperature on the Conformations of Electrosprayed Ions: Unfolding of Compact Ubiquitin Conformers from Pseudonative and Denatured Solutions
  publication-title: Int. J. Mass Spectrom.
  doi: 10.1016/S1387-3806(98)14135-0
– volume: 144–145
  start-page: 97
  year: 2024
  ident: ref_9
  article-title: NMR Investigations of Glycan Conformation, Dynamics, and Interactions
  publication-title: Prog. Nucl. Magn. Reson. Spectrosc.
  doi: 10.1016/j.pnmrs.2024.10.002
– volume: 141
  start-page: 14463
  year: 2019
  ident: ref_5
  article-title: Advancing Solutions to the Carbohydrate Sequencing Challenge
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.9b06406
– volume: 96
  start-page: 683
  year: 1996
  ident: ref_4
  article-title: Glycobiology: Toward Understanding the Function of Sugars
  publication-title: Chem. Rev.
  doi: 10.1021/cr940283b
– volume: 31
  start-page: 445
  year: 1996
  ident: ref_33
  article-title: Internal energy effects in mass spectrometry
  publication-title: J. Mass Spectrom.
  doi: 10.1002/(SICI)1096-9888(199605)31:5<445::AID-JMS354>3.0.CO;2-G
– volume: 33
  start-page: 1772
  year: 2022
  ident: ref_19
  article-title: A Data Set of Ion Mobility Collision Cross Sections and Liquid Chromatography Retention Times from 71 Pyridylaminated N-Linked Oligosaccharides
  publication-title: J. Am. Soc. Mass Spectrom.
  doi: 10.1021/jasms.2c00165
– volume: 231
  start-page: 189
  year: 2004
  ident: ref_26
  article-title: Influence of the capillary temperature and the source pressure on the internal energy distribution of electrosprayed ions
  publication-title: Int. J. Mass Spectrom.
  doi: 10.1016/j.ijms.2003.10.010
– volume: 15
  start-page: 113
  year: 2009
  ident: ref_27
  article-title: Deciphering Drift Time Measurements from Travelling Wave Ion Mobility Spectrometry-Mass Spectrometry Studies
  publication-title: Eur. J. Mass Spectrom.
  doi: 10.1255/ejms.947
– volume: 30
  start-page: 11
  year: 2013
  ident: ref_6
  article-title: Glycomics Using Mass Spectrometry
  publication-title: Glycoconj. J.
  doi: 10.1007/s10719-012-9376-3
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Snippet The structural analysis of glycans remains a major challenge due to their high isomeric complexity and conformational flexibility arising from diverse...
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StartPage 2177
SubjectTerms Analysis
Carbohydrates
conformational dynamics
electrospray ionization
glycans
Ion Mobility Spectrometry
Ionization
Ions - chemistry
Mass Spectrometry
NMR
Nuclear magnetic resonance
Polysaccharides
Polysaccharides - chemistry
Scientific imaging
Sodium
Sodium - chemistry
Solvents
Solvents - chemistry
Temperature
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Title Effects of Different Adduct Ions, Ionization Temperatures, and Solvents on the Ion Mobility of Glycans
URI https://www.ncbi.nlm.nih.gov/pubmed/40430350
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https://doaj.org/article/c773763ce5c5424ab600a594be7f1b2c
Volume 30
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