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Deciphering mouse brain spatial diversity via glyco-lipidomic mapping

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dc.contributor.authorLee, Jua-
dc.contributor.authorYin, Dongtan-
dc.contributor.authorYun, Jaekyung-
dc.contributor.authorMinsoo Kim-
dc.contributor.authorSeong-Wook Kim-
dc.contributor.authorHwang, Heeyoun-
dc.contributor.authorPark, Ji Eun-
dc.contributor.authorBoyoung Lee-
dc.contributor.authorC. Justin Lee-
dc.contributor.authorHee-Sup Shin-
dc.contributor.authorAn, Hyun Joo-
dc.date.accessioned2025-01-14T02:00:09Z-
dc.date.available2025-01-14T02:00:09Z-
dc.date.created2024-10-21-
dc.date.issued2024-10-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/16153-
dc.description.abstractGangliosides in the brain play a crucial role in modulating the integrity of vertebrate central nervous system in a region-specific manner. However, to date, a comprehensive structural elucidation of complex intact ganglioside isomers has not been achieved, resulting in the elusiveness into related molecular mechanism. Here, we present a glycolipidomic approach for isomer-specific and brain region-specific profiling of the mouse brain. Considerable region-specificity and commonality in specific group of regions are highlighted. Notably, we observe a similarity in the abundance of major isomers, GD1a and GD1b, within certain regions, which provides significant biological implications with interpretation through the lens of a theoretical retrosynthetic state-transition network. Furthermore, A glycocentric-omics approaches using gangliosides and N-glycans reveal a remarkable convergence in spatial dynamics, providing valuable insight into molecular interaction network. Collectively, this study uncovers the spatial dynamics of intact glyco-conjugates in the brain, which are relevant to regional function and accelerates the discovery of potential therapeutic targets for brain diseases. © The Author(s) 2024.-
dc.language영어-
dc.publisherNature Publishing Group-
dc.titleDeciphering mouse brain spatial diversity via glyco-lipidomic mapping-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid001330698100009-
dc.identifier.scopusid2-s2.0-85205793015-
dc.identifier.rimsid84259-
dc.contributor.affiliatedAuthorMinsoo Kim-
dc.contributor.affiliatedAuthorSeong-Wook Kim-
dc.contributor.affiliatedAuthorBoyoung Lee-
dc.contributor.affiliatedAuthorC. Justin Lee-
dc.contributor.affiliatedAuthorHee-Sup Shin-
dc.identifier.doi10.1038/s41467-024-53032-8-
dc.identifier.bibliographicCitationNature Communications, v.15, no.1-
dc.relation.isPartOfNature Communications-
dc.citation.titleNature Communications-
dc.citation.volume15-
dc.citation.number1-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalWebOfScienceCategoryMultidisciplinary Sciences-
dc.subject.keywordPlusALZHEIMERS-DISEASE-
dc.subject.keywordPlusMASS-SPECTROMETRY-
dc.subject.keywordPlusTISSUE SECTIONS-
dc.subject.keywordPlusPATHOGENIC ROLE-
dc.subject.keywordPlusGLYCOSPHINGOLIPIDS-
dc.subject.keywordPlusLOCALIZATION-
dc.subject.keywordPlusBIOSYNTHESIS-
dc.subject.keywordPlusDEFICIENCY-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusGANGLIOSIDE METABOLISM-
Appears in Collections:
Center for Cognition and Sociality(인지 및 사회성 연구단) > 1. Journal Papers (저널논문)
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