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Detection and destruction of HER2-positive cancer cells by Ultra Quenchbody-siRNA complex

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dc.contributor.authorDong, Jinhua-
dc.contributor.authorOka, Yuya-
dc.contributor.authorJeong, Hee-Jin-
dc.contributor.authorOhmuro-Matsuyama, Yuki-
dc.contributor.authorUeda, Hiroshi-
dc.date.available2020-07-10T07:42:23Z-
dc.date.created2020-07-06-
dc.date.issued2020-05-
dc.identifier.issn0006-3592-
dc.identifier.urihttps://scholarworks.bwise.kr/hongik/handle/2020.sw.hongik/10984-
dc.description.abstractUltra Quenchbody (UQ-body) is a biosensor that utilizes the quenching behavior of the fluorescent dye linked to the antibody V region. When the corresponding antigen is bound to the UQ-body, the fluorescence is restored and allows the detection of target molecules easily and sensitively. In this paper, we constructed UQ-bodies to sensitively detect the human epidermal growth factor receptor 2 (HER2) cancer marker in solution or on cancer cells, which was further used to kill the cancer cells. A synthetic Fab fragment of anti-HER2 antibody Fab37 with many Trp residues at hypervariable region was prepared and labeled with fluorescent dyes to obtain the UQ-bodies. The UQ-body could detect HER2 in solution at concentrations as low as 20 pM with an EC50 of 0.3 nM with a fourfold response. Fluorescence imaging of HER2-positive cells was successfully performed without any washing steps. To deliver small interfering RNA (siRNA) to cancer cells, a modified UQ-body with C-terminal 9R sequence was also prepared. HER2-positive cancer cells were effectively killed by polo-like kinase 1 siRNA intracellularly delivered by the UQ-body-9R. The novel approach employing siRNA-empowered UQ-body could detect and image the HER2 antigen easily and sensitively, and effectively kill the HER2-positive cancer cells.-
dc.language영어-
dc.language.isoen-
dc.publisherWILEY-
dc.titleDetection and destruction of HER2-positive cancer cells by Ultra Quenchbody-siRNA complex-
dc.typeArticle-
dc.contributor.affiliatedAuthorJeong, Hee-Jin-
dc.identifier.doi10.1002/bit.27302-
dc.identifier.scopusid2-s2.0-85079706185-
dc.identifier.wosid000513735300001-
dc.identifier.bibliographicCitationBIOTECHNOLOGY AND BIOENGINEERING, v.117, no.5, pp.1259 - 1269-
dc.relation.isPartOfBIOTECHNOLOGY AND BIOENGINEERING-
dc.citation.titleBIOTECHNOLOGY AND BIOENGINEERING-
dc.citation.volume117-
dc.citation.number5-
dc.citation.startPage1259-
dc.citation.endPage1269-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass3-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.subject.keywordPlusANTIBODY-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusDYES-
dc.subject.keywordAuthorantibody drug conjugate-
dc.subject.keywordAuthorcancer imaging-
dc.subject.keywordAuthorfluorescence quenching-
dc.subject.keywordAuthorhigh throughput screening-
dc.subject.keywordAuthorpolo-like kinase-
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