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dc.contributor.authorHan, Sang-Soo-
dc.contributor.authorLee, Dong-Eun-
dc.contributor.authorShim, Hye-Eun-
dc.contributor.authorLee, Sangmin-
dc.contributor.authorJung, Taekhee-
dc.contributor.authorOh, Jung-Hwa-
dc.contributor.authorLee, Hyang-Ae-
dc.contributor.authorMoon, Sung-Hwan-
dc.contributor.authorJeon, Jongho-
dc.contributor.authorYoon, Seokjoo-
dc.contributor.authorKim, Kwangmeyung-
dc.contributor.authorKang, Sun-Woong-
dc.date.accessioned2024-01-20T02:02:06Z-
dc.date.available2024-01-20T02:02:06Z-
dc.date.created2021-09-05-
dc.date.issued2017-03-
dc.identifier.issn1838-7640-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/122980-
dc.description.abstractMetabolic labeling techniques are powerful tools for cell labeling, tracking and proteomic analysis. However, at present, the effects of the metabolic labeling agents on cell metabolism and physiology are not known. To address this question, in this study, we analyzed the effects of cells treated with Ac4ManNAz through microarray analysis and analyses of membrane channel activity, individual bio-physiological properties, and glycolytic flux. According to the results, treatment with 50 mu M Ac4ManNAz led to the reduction of major cellular functions, including energy generation capacity, cellular infiltration ability and channel activity. Interestingly, 10 mu M Ac4ManNAz showed the least effect on cellular systems and had a sufficient labeling efficiency for cell labeling, tracking and proteomic analysis. Based on our results, we suggest 10 mu M as the optimum concentration of Ac4ManNAz for in vivo cell labeling and tracking. Additionally, we expect that our approach could be used for cell-based therapy for monitoring the efficacy of molecule delivery and the fate of recipient cells.-
dc.languageEnglish-
dc.publisherIVYSPRING INT PUBL-
dc.subjectCLICK CHEMISTRY-
dc.subjectQUANTITATIVE PROTEOMICS-
dc.subjectSIGNALING PATHWAYS-
dc.subjectN-GLYCOSYLATION-
dc.subjectLIVING ANIMALS-
dc.subjectAZIDO SUGARS-
dc.subjectTHERAPY-
dc.subjectGLYCANS-
dc.subjectDEATH-
dc.subjectBIOCONJUGATION-
dc.titlePhysiological Effects of Ac4ManNAz and Optimization of Metabolic Labeling for Cell Tracking-
dc.typeArticle-
dc.identifier.doi10.7150/thno.17711-
dc.description.journalClass1-
dc.identifier.bibliographicCitationTHERANOSTICS, v.7, no.5, pp.1164 - 1176-
dc.citation.titleTHERANOSTICS-
dc.citation.volume7-
dc.citation.number5-
dc.citation.startPage1164-
dc.citation.endPage1176-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000396574200010-
dc.identifier.scopusid2-s2.0-85014582959-
dc.relation.journalWebOfScienceCategoryMedicine, Research & Experimental-
dc.relation.journalResearchAreaResearch & Experimental Medicine-
dc.type.docTypeArticle-
dc.subject.keywordPlusCLICK CHEMISTRY-
dc.subject.keywordPlusQUANTITATIVE PROTEOMICS-
dc.subject.keywordPlusSIGNALING PATHWAYS-
dc.subject.keywordPlusN-GLYCOSYLATION-
dc.subject.keywordPlusLIVING ANIMALS-
dc.subject.keywordPlusAZIDO SUGARS-
dc.subject.keywordPlusTHERAPY-
dc.subject.keywordPlusGLYCANS-
dc.subject.keywordPlusDEATH-
dc.subject.keywordPlusBIOCONJUGATION-
dc.subject.keywordAuthorMetabolic labeling-
dc.subject.keywordAuthorAzido-sugar-
dc.subject.keywordAuthorModified glycosylation-
dc.subject.keywordAuthorAzido group-
dc.subject.keywordAuthorPhysiology-
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KIST Article > 2017
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