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The box a domain of high mobility group box-1 protein as an efficient siRNA carrier with anti-inflammatory effects

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dc.contributor.authorLee, Sanghyun-
dc.contributor.authorSong, Hojung-
dc.contributor.authorKim, Hyun Ah-
dc.contributor.authorOh, Binna-
dc.contributor.authorLee, Dong Yun-
dc.contributor.authorLee, Minhyung-
dc.date.accessioned2022-07-16T17:06:03Z-
dc.date.available2022-07-16T17:06:03Z-
dc.date.issued2012-01-
dc.identifier.issn0730-2312-
dc.identifier.issn1097-4644-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/166523-
dc.description.abstractHigh mobility group box-1 (HMGB-1) is a DNA binding nuclear protein and pro-inflammatory cytokine. The box A domain of HMGB-1 (rHMGB-1A) exerts an anti-inflammatory effect, inhibiting wild-type HMGB-1 (wtHMGB-1). In this study, HMGB-1A was evaluated as an siRNA carrier with anti-inflammatory effects. HMGB-1A was expressed and purified by consecutive nickel chelate chromatography, cationic exchange chromatography, and polymixin B chromatography. Purified rHMGB-1A demonstrated an anti-inflammatory effect, reducing tumor necrosis factor-a (TNF-a) in wtHMGB-1 or lipopolysaccharide (LPS) activated macrophages. In gel retardation assay, rHMGB-1A formed a stable complex with siRNA at or above a 1:2 weight ratio (siRNA:rHMGB-1A). A heparin competition assay showed that an siRNA/rHMGB-1A complex released siRNA more easily than an siRNA/polyethylenimine (PEI, 25 kDa) complex. Luciferase siRNA/rHMGB-1A reduced firefly luciferase expression at a similar level as luciferase siRNA/PEI complex. Furthermore, TNF-a siRNA/rHMGB-1A synergistically reduced TNF-a expression in LPS activated macrophages. Therefore, rHMGB-1A may be useful as an siRNA carrier with anti-inflammatory effects in siRNA therapy for various inflammatory diseases.-
dc.format.extent10-
dc.language영어-
dc.language.isoENG-
dc.publisherJohn Wiley & Sons Inc.-
dc.titleThe box a domain of high mobility group box-1 protein as an efficient siRNA carrier with anti-inflammatory effects-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1002/jcb.23334-
dc.identifier.scopusid2-s2.0-84055222636-
dc.identifier.wosid000298598300014-
dc.identifier.bibliographicCitationJournal of Cellular Biochemistry, v.113, no.1, pp 122 - 131-
dc.citation.titleJournal of Cellular Biochemistry-
dc.citation.volume113-
dc.citation.number1-
dc.citation.startPage122-
dc.citation.endPage131-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaCell Biology-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryCell Biology-
dc.subject.keywordPlusGLYCATION END-PRODUCTS-
dc.subject.keywordPlusDNA-BINDING CYTOKINE-
dc.subject.keywordPlusNF-KAPPA-B-
dc.subject.keywordPlusGENE DELIVERY-
dc.subject.keywordPlusNUCLEIC-ACIDS-
dc.subject.keywordPlusIN-VIVO-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusINFLAMMATION-
dc.subject.keywordPlusPEPTIDE-
dc.subject.keywordPlusHMGB-1-
dc.subject.keywordAuthorHigh mobility group box-1-
dc.subject.keywordAuthorGene therapy-
dc.subject.keywordAuthorAnti-inflammation-
dc.subject.keywordAuthorRecombinant peptide-
dc.subject.keywordAuthorsiRNA delivery-
dc.identifier.urlhttps://onlinelibrary.wiley.com/doi/10.1002/jcb.23334-
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