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dc.contributor.authorHsu, Jen-Fangen_US
dc.contributor.authorHsieh, Pei-Yingen_US
dc.contributor.authorHsu, Hsin-Yunen_US
dc.contributor.authorShigeto, Shinsukeen_US
dc.date.accessioned2019-04-03T06:44:37Z-
dc.date.available2019-04-03T06:44:37Z-
dc.date.issued2015-12-03en_US
dc.identifier.issn2045-2322en_US
dc.identifier.urihttp://dx.doi.org/10.1038/srep17541en_US
dc.identifier.urihttp://hdl.handle.net/11536/129339-
dc.description.abstractIn vivo, molecular-level investigation of cytokinesis, the climax of the cell cycle, not only deepens our understanding of how life continues, but it will also open up new possibilities of diagnosis/prognosis of cancer cells. Although fluorescence-based methods have been widely employed to address this challenge, they require a fluorophore to be designed for a specific known biomolecule and introduced into the cell. Here, we present a label-free spectral imaging approach based on multivariate curve resolution analysis of Raman hyperspectral data that enables exploratory untargeted studies of mammalian cell cytokinesis. We derived intrinsic vibrational spectra and intracellular distributions of major biomolecular components (lipids and proteins) in dividing and nondividing human colon cancer cells. In addition, we discovered an unusual autofluorescent lipid component that appears predominantly in the vicinity of the cleavage furrow during cytokinesis. This autofluorescence signal could be utilized as an endogenous probe for monitoring and visualizing cytokinesis in vivo.en_US
dc.language.isoen_USen_US
dc.titleWhen cells divide: Label-free multimodal spectral imaging for exploratory molecular investigation of living cells during cytokinesisen_US
dc.typeArticleen_US
dc.identifier.doi10.1038/srep17541en_US
dc.identifier.journalSCIENTIFIC REPORTSen_US
dc.citation.volume5en_US
dc.citation.spage0en_US
dc.citation.epage0en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.department應用化學系分子科學碩博班zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.contributor.departmentInstitute of Molecular scienceen_US
dc.identifier.wosnumberWOS:000365689800003en_US
dc.citation.woscount12en_US
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