Deciphering mouse brain spatial diversity via glyco-lipidomic mapping
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Lee, Jua | - |
dc.contributor.author | Yin, Dongtan | - |
dc.contributor.author | Yun, Jaekyung | - |
dc.contributor.author | Minsoo Kim | - |
dc.contributor.author | Seong-Wook Kim | - |
dc.contributor.author | Hwang, Heeyoun | - |
dc.contributor.author | Park, Ji Eun | - |
dc.contributor.author | Boyoung Lee | - |
dc.contributor.author | C. Justin Lee | - |
dc.contributor.author | Hee-Sup Shin | - |
dc.contributor.author | An, Hyun Joo | - |
dc.date.accessioned | 2025-01-14T02:00:09Z | - |
dc.date.available | 2025-01-14T02:00:09Z | - |
dc.date.created | 2024-10-21 | - |
dc.date.issued | 2024-10 | - |
dc.identifier.uri | https://pr.ibs.re.kr/handle/8788114/16153 | - |
dc.description.abstract | Gangliosides 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.language | 영어 | - |
dc.publisher | Nature Publishing Group | - |
dc.title | Deciphering mouse brain spatial diversity via glyco-lipidomic mapping | - |
dc.type | Article | - |
dc.type.rims | ART | - |
dc.identifier.wosid | 001330698100009 | - |
dc.identifier.scopusid | 2-s2.0-85205793015 | - |
dc.identifier.rimsid | 84259 | - |
dc.contributor.affiliatedAuthor | Minsoo Kim | - |
dc.contributor.affiliatedAuthor | Seong-Wook Kim | - |
dc.contributor.affiliatedAuthor | Boyoung Lee | - |
dc.contributor.affiliatedAuthor | C. Justin Lee | - |
dc.contributor.affiliatedAuthor | Hee-Sup Shin | - |
dc.identifier.doi | 10.1038/s41467-024-53032-8 | - |
dc.identifier.bibliographicCitation | Nature Communications, v.15, no.1 | - |
dc.relation.isPartOf | Nature Communications | - |
dc.citation.title | Nature Communications | - |
dc.citation.volume | 15 | - |
dc.citation.number | 1 | - |
dc.description.journalClass | 1 | - |
dc.description.journalClass | 1 | - |
dc.description.isOpenAccess | Y | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalWebOfScienceCategory | Multidisciplinary Sciences | - |
dc.subject.keywordPlus | ALZHEIMERS-DISEASE | - |
dc.subject.keywordPlus | MASS-SPECTROMETRY | - |
dc.subject.keywordPlus | TISSUE SECTIONS | - |
dc.subject.keywordPlus | PATHOGENIC ROLE | - |
dc.subject.keywordPlus | GLYCOSPHINGOLIPIDS | - |
dc.subject.keywordPlus | LOCALIZATION | - |
dc.subject.keywordPlus | BIOSYNTHESIS | - |
dc.subject.keywordPlus | DEFICIENCY | - |
dc.subject.keywordPlus | EXPRESSION | - |
dc.subject.keywordPlus | GANGLIOSIDE METABOLISM | - |