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Supramolecular Analysis of Monosaccharide Derivatives Using Cucurbit[7]uril and Electrospray Ionization Tandem Mass Spectrometry

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dc.contributor.authorLee, Hyun Hee L.-
dc.contributor.authorKim, Hugh I.-
dc.date.accessioned2021-09-02T12:50:36Z-
dc.date.available2021-09-02T12:50:36Z-
dc.date.created2021-06-16-
dc.date.issued2018-04-
dc.identifier.issn0021-2148-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/76218-
dc.description.abstractIdentification of monosaccharide derivatives using an analytical technique is difficult due to their isomeric structures and similar physical properties. Although mass spectrometry (MS) has emerged as a prominent technique for this purpose, a comprehensive MS-based method for analyzing diverse monosaccharide species is yet to be developed. Herein, we employ host-guest chemistry using cucurbit[7]uril (CB[7]) with MS to identify four different monosaccharide derivative species. Tandem MS analysis distinguishes the monosaccharide derivatives based on the unique fragmentation pattern produced when forming gas-phase complexes with CB[7]. The ion mobility studies combined with computational calculations reveal that subtle differences in isomers cause distinct orientations inside CB[7] cavity, resulting in different fragmentation patterns of the isomers. This unique study demonstrates that host-guest chemistry combined with MS can be used for developing effective isomer analysis techniques.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherWILEY-V C H VERLAG GMBH-
dc.subjectDIASTEREOMERIC HEXOSAMINE MONOSACCHARIDES-
dc.subjectHIGH-AFFINITY BINDING-
dc.subjectSTEREOCHEMICAL DIFFERENTIATION-
dc.subjectUNDERIVATIZED MONOSACCHARIDES-
dc.subjectSTRUCTURAL-CHARACTERIZATION-
dc.subjectCELL-ADHESION-
dc.subjectGAS-PHASE-
dc.subjectCHEMISTRY-
dc.subjectGLYCOSYLATION-
dc.subjectWATER-
dc.titleSupramolecular Analysis of Monosaccharide Derivatives Using Cucurbit[7]uril and Electrospray Ionization Tandem Mass Spectrometry-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Hugh I.-
dc.identifier.doi10.1002/ijch.201700073-
dc.identifier.scopusid2-s2.0-85029039970-
dc.identifier.wosid000430466900023-
dc.identifier.bibliographicCitationISRAEL JOURNAL OF CHEMISTRY, v.58, no.3-4, pp.472 - 478-
dc.relation.isPartOfISRAEL JOURNAL OF CHEMISTRY-
dc.citation.titleISRAEL JOURNAL OF CHEMISTRY-
dc.citation.volume58-
dc.citation.number3-4-
dc.citation.startPage472-
dc.citation.endPage478-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusDIASTEREOMERIC HEXOSAMINE MONOSACCHARIDES-
dc.subject.keywordPlusHIGH-AFFINITY BINDING-
dc.subject.keywordPlusSTEREOCHEMICAL DIFFERENTIATION-
dc.subject.keywordPlusUNDERIVATIZED MONOSACCHARIDES-
dc.subject.keywordPlusSTRUCTURAL-CHARACTERIZATION-
dc.subject.keywordPlusCELL-ADHESION-
dc.subject.keywordPlusGAS-PHASE-
dc.subject.keywordPlusCHEMISTRY-
dc.subject.keywordPlusGLYCOSYLATION-
dc.subject.keywordPlusWATER-
dc.subject.keywordAuthorcarbohydrates-
dc.subject.keywordAuthorhost-guest systems-
dc.subject.keywordAuthormass spectrometry-
dc.subject.keywordAuthorsupramolecular chemistry-
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