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Cited 2 time in webofscience Cited 2 time in scopus
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dc.contributor.authorKim, JH-
dc.contributor.authorLee, MJ-
dc.contributor.authorHwang, I-
dc.contributor.authorHwang, HJ-
dc.date.accessioned2015-06-25T03:24:49Z-
dc.date.available2015-06-25T03:24:49Z-
dc.date.created2014-03-18-
dc.date.issued2013-03-21-
dc.identifier.issn1932-6203-
dc.identifier.other2015-OAK-0000029586en_US
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/12679-
dc.description.abstractThis study describes a sensitive in-cell protease detection system that enables direct fluorescence detection of a target protease and its inhibition inside living cells. This live-cell imaging system provides a fluorescent molecular beacon protein comprised of an intracellular translocation signal sequence, a protease-specific cleavage sequence, and a fluorescent tag sequence(s). The molecular beacon protein is designed to change its intracellular localization upon cleavage by a target protease, i.e., from the cytosol to a subcellular organelle or from a subcellular organelle to the cytosol. Protease activity can be monitored at the single cell level, and accordingly the entire cell population expressing the protease can be accurately enumerated. The clear cellular change in fluorescence pattern makes this system an ideal tool for various life science and drug discovery research, including high throughput and high content screening applications.-
dc.description.statementofresponsibilityopenen_US
dc.languageEnglish-
dc.publisherspringer-
dc.relation.isPartOfPLoS one-
dc.rightsBY_NC_NDen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/2.0/kren_US
dc.titleIn-cell protease assay systems based on trans-localizing molecular beacon proteins using HCV protease as a model system.-
dc.typeArticle-
dc.contributor.college융합생명공학부en_US
dc.identifier.doi10.1371/JOURNAL.PONE.0059710-
dc.author.googleKim, JHen_US
dc.author.googleLee, MJen_US
dc.author.googleHwang, HJen_US
dc.author.googleHwang, Ien_US
dc.relation.volume8en_US
dc.relation.issue3en_US
dc.contributor.id10078446en_US
dc.relation.journalPLoS oneen_US
dc.relation.indexSCI급, SCOPUS 등재논문en_US
dc.relation.sciSCIen_US
dc.collections.nameJournal Papersen_US
dc.type.rimsART-
dc.identifier.bibliographicCitationPLoS one, v.8, no.3-
dc.identifier.wosid000316546400055-
dc.date.tcdate2019-01-01-
dc.citation.number3-
dc.citation.titlePLoS one-
dc.citation.volume8-
dc.contributor.affiliatedAuthorHwang, I-
dc.identifier.scopusid2-s2.0-84875311675-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc1-
dc.description.scptc2*
dc.date.scptcdate2018-10-274*
dc.type.docTypeArticle-
dc.subject.keywordPlusHEPATITIS-C-
dc.subject.keywordPlusPHOSPHORYLATION-
dc.subject.keywordPlusBOCEPREVIR-
dc.subject.keywordPlusINHIBITORS-
dc.subject.keywordPlusDIVERSITY-
dc.subject.keywordPlusAPOPTOSIS-
dc.subject.keywordPlusBETA-
dc.relation.journalWebOfScienceCategoryMultidisciplinary Sciences-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaScience & Technology - Other Topics-

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황인환HWANG, INHWAN
Dept of Life Sciences
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