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Delivery of shRNA using gold nanoparticle-DNA oligonucleotide conjugates as a universal carrier

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dc.contributor.authorRyou, Sang-Mi-
dc.contributor.authorKim, Sudeok-
dc.contributor.authorJang, Hyun Hye-
dc.contributor.authorKim, Jae-Hong-
dc.contributor.authorYeom, Ji-Hyun-
dc.contributor.authorEom, Min Sik-
dc.contributor.authorBae, Jeehyeon-
dc.contributor.authorHan, Min Su-
dc.contributor.authorLee, Kangseok-
dc.date.available2019-05-30T00:57:25Z-
dc.date.issued2010-07-
dc.identifier.issn0006-291X-
dc.identifier.issn1090-2104-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/22320-
dc.description.abstractThe efficient delivery of nucleic acids into mammalian cells is a central aspect of research involving cell biology and medical applications, including the clinical treatment of genetic disorders. We report an efficient small hairpin RNA (shRNA) delivery system that utilizes a single species of gold nanoparticle-DNA oligonucleotide conjugate (AuNP-DNA oligo) as a universal carrier. In vitro synthesized shRNA that is specific to the p53 gene was efficiently delivered into HEK293 and HeLa human cell lines using an AuNP-DNA oligo. The delivery resulted in an 80-90% knockdown of p53 expression. The same AuNP-DNA oligo was also efficient for the delivery of another shRNA, which is specific to the Mcl-1 gene, as well as the repression of MCL-1 expression. The knockdown efficiency of shRNA that was delivered using an AuNP-DNA oligo was comparable with that of a liposome-based shRNA delivery method. Our results offer an alternate delivery system for shRNA that can be used on any gene of interest. (C) 2010 Elsevier Inc. All rights reserved.-
dc.format.extent5-
dc.language영어-
dc.language.isoENG-
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCE-
dc.titleDelivery of shRNA using gold nanoparticle-DNA oligonucleotide conjugates as a universal carrier-
dc.typeArticle-
dc.identifier.doi10.1016/j.bbrc.2010.06.115-
dc.identifier.bibliographicCitationBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.398, no.3, pp 542 - 546-
dc.description.isOpenAccessN-
dc.identifier.wosid000280867400036-
dc.identifier.scopusid2-s2.0-77955279049-
dc.citation.endPage546-
dc.citation.number3-
dc.citation.startPage542-
dc.citation.titleBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.citation.volume398-
dc.type.docTypeArticle-
dc.publisher.location미국-
dc.subject.keywordAuthorGold nanoparticle-
dc.subject.keywordAuthorGene delivery system-
dc.subject.keywordAuthorGene knockdown-
dc.subject.keywordAuthorshRNA-
dc.subject.keywordPlusMAMMALIAN-CELLS-
dc.subject.keywordPlusCONTROLLED-RELEASE-
dc.subject.keywordPlusGENE-REGULATION-
dc.subject.keywordPlusDRUG-DELIVERY-
dc.subject.keywordPlusTRANSFECTION-
dc.subject.keywordPlusBIOLOGY-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiophysics-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiophysics-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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