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Highly effective detection of inflamed cells using a modified bradykinin ligand labeled with FITC fluorescence

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dc.contributor.authorYeo, Ki Baek-
dc.contributor.authorKim, Hyong Bai-
dc.contributor.authorChoi, Yoo Seong-
dc.contributor.authorPack, Seung Pil-
dc.date.accessioned2021-09-04T04:22:05Z-
dc.date.available2021-09-04T04:22:05Z-
dc.date.created2021-06-18-
dc.date.issued2016-01-
dc.identifier.issn0141-0229-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/89889-
dc.description.abstractDetection of inflammation in live cells is important because long-lasting inflammation is considered to be a primary cause of several diseases. However, few reports have been published on imaging analysis of inflammation in live cells. In this study, we developed an effective imaging system for detection of inflamed cells using a bradykinin ligand (BK) or a modified BK (mBK), which has specific affinity with the cellular B1R receptor. Synthetic BK or mBK labeled with FITC at the N-terminus was employed for discriminating between inflamed and normal cells; this method was found to be effective for detection of inflammation in live cells. In addition, using the mBK-based cell imaging system, we successfully performed flow-based analysis of live cell inflammation on a micro-chip channel, composed of a Starna flow cell and PDMS (Polydimethylsiloxane) walls. The BK-based cell imaging methods designed here would be a useful platform for development of a high-throughput live cell analysis system for investigating the factors underlying inflammation or for screening of anti-inflammation candidate drugs. (C) 2015 Elsevier Inc. All rights reserved.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherELSEVIER SCIENCE INC-
dc.subjectCHEMICAL FIXATION-
dc.subjectRECEPTOR-
dc.subjectINFLAMMATION-
dc.subjectB1-
dc.subjectB2-
dc.titleHighly effective detection of inflamed cells using a modified bradykinin ligand labeled with FITC fluorescence-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Hyong Bai-
dc.contributor.affiliatedAuthorPack, Seung Pil-
dc.identifier.doi10.1016/j.enzmictec.2015.10.008-
dc.identifier.scopusid2-s2.0-84947969337-
dc.identifier.wosid000368381200026-
dc.identifier.bibliographicCitationENZYME AND MICROBIAL TECHNOLOGY, v.82, pp.191 - 196-
dc.relation.isPartOfENZYME AND MICROBIAL TECHNOLOGY-
dc.citation.titleENZYME AND MICROBIAL TECHNOLOGY-
dc.citation.volume82-
dc.citation.startPage191-
dc.citation.endPage196-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.subject.keywordPlusCHEMICAL FIXATION-
dc.subject.keywordPlusRECEPTOR-
dc.subject.keywordPlusINFLAMMATION-
dc.subject.keywordPlusB1-
dc.subject.keywordPlusB2-
dc.subject.keywordAuthorInflammation-
dc.subject.keywordAuthorBradykinin-
dc.subject.keywordAuthorLive cell imaging-
dc.subject.keywordAuthorFlow-based cell analysis-
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