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Label-free and live cell imaging by interferometric scattering microscopy

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dc.contributor.authorPark, Jin-Sung-
dc.contributor.authorLee, Il-Buem-
dc.contributor.authorMoon, Hyeon-Min-
dc.contributor.authorJoo, Jong-Hyeon-
dc.contributor.authorKim, Kyoung-Hoon-
dc.contributor.authorHong, Seok-Cheol-
dc.contributor.authorCho, Minhaeng-
dc.date.accessioned2021-09-02T13:47:09Z-
dc.date.available2021-09-02T13:47:09Z-
dc.date.created2021-06-16-
dc.date.issued2018-03-14-
dc.identifier.issn2041-6520-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/76731-
dc.description.abstractDespite recent remarkable advances in microscopic techniques, it still remains very challenging to directly observe the complex structure of cytoplasmic organelles in live cells without a fluorescent label. Here we report label-free and live-cell imaging of mammalian cell, Escherischia coli, and yeast, using interferometric scattering microscopy, which reveals the underlying structures of a variety of cytoplasmic organelles as well as the underside structure of the cells. The contact areas of the cells attached onto a glass substrate, e.g., focal adhesions and filopodia, are clearly discernible. We also found a variety of fringe-like features in the cytoplasmic area, which may reflect the folded structures of cytoplasmic organelles. We thus anticipate that the label-free interferometric scattering microscopy can be used as a powerful tool to shed interferometric light on in vivo structures and dynamics of various intracellular phenomena.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherROYAL SOC CHEMISTRY-
dc.subjectCOHERENT BRIGHTFIELD MICROSCOPY-
dc.subjectSINGLE-MOLECULE LEVEL-
dc.subjectREFRACTIVE-INDEX-
dc.subjectGENERATION MICROSCOPY-
dc.subjectCARS MICROSCOPY-
dc.subjectLIVING CELLS-
dc.subjectTRACKING-
dc.subjectSPEED-
dc.subjectMITOCHONDRIA-
dc.subjectDYNAMICS-
dc.titleLabel-free and live cell imaging by interferometric scattering microscopy-
dc.typeArticle-
dc.contributor.affiliatedAuthorHong, Seok-Cheol-
dc.contributor.affiliatedAuthorCho, Minhaeng-
dc.identifier.doi10.1039/c7sc04733a-
dc.identifier.scopusid2-s2.0-85043481891-
dc.identifier.wosid000431100300005-
dc.identifier.bibliographicCitationCHEMICAL SCIENCE, v.9, no.10, pp.2690 - 2697-
dc.relation.isPartOfCHEMICAL SCIENCE-
dc.citation.titleCHEMICAL SCIENCE-
dc.citation.volume9-
dc.citation.number10-
dc.citation.startPage2690-
dc.citation.endPage2697-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusCOHERENT BRIGHTFIELD MICROSCOPY-
dc.subject.keywordPlusSINGLE-MOLECULE LEVEL-
dc.subject.keywordPlusREFRACTIVE-INDEX-
dc.subject.keywordPlusGENERATION MICROSCOPY-
dc.subject.keywordPlusCARS MICROSCOPY-
dc.subject.keywordPlusLIVING CELLS-
dc.subject.keywordPlusTRACKING-
dc.subject.keywordPlusSPEED-
dc.subject.keywordPlusMITOCHONDRIA-
dc.subject.keywordPlusDYNAMICS-
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