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dc.contributor.authorChang, Wei-Tienen_US
dc.contributor.authorYang, Yi-Cyunen_US
dc.contributor.authorLu, Hsueh-Hanen_US
dc.contributor.authorLi, I-Linen_US
dc.contributor.authorLiau, Ianen_US
dc.date.accessioned2014-12-08T15:07:24Z-
dc.date.available2014-12-08T15:07:24Z-
dc.date.issued2010-02-17en_US
dc.identifier.issn0002-7863en_US
dc.identifier.urihttp://dx.doi.org/10.1021/ja9086038en_US
dc.identifier.urihttp://hdl.handle.net/11536/5830-
dc.description.abstractThe ability to generate antimicrobial reactive-oxygen species (ROS) by reduced nicotinamide adenine dinucleotide phosphate (NADPH) oxidase is critical for the host to defend against invading microbes. We have demonstrated the application of confocal autofluorescence microscopy and Raman microspectroscopy to characterize dynamically the phagocytic process of living macrophages in a label-free manner. In particular, we visualized the translocation of NADPH oxidases in livin macrophages that are undergoing phagocytosis of invading yeasts and monitored dynamically the change at the molecular level of single intraphagosomal yeasts caused by phagocytic ROS.en_US
dc.language.isoen_USen_US
dc.titleSpatiotemporal Characterization of Phagocytic NADPH Oxidase and Oxidative Destruction of Intraphagosomal Organisms in Vivo Using Autofluorescence Imaging and Raman Microspectroscopyen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/ja9086038en_US
dc.identifier.journalJOURNAL OF THE AMERICAN CHEMICAL SOCIETYen_US
dc.citation.volume132en_US
dc.citation.issue6en_US
dc.citation.spage1744en_US
dc.citation.epage+en_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:000275085000006-
dc.citation.woscount9-
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