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Low molecular weight polyethylenimine-mitochondrial leader peptide conjugate for DNA delivery to mitochondria

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dc.contributor.authorChoi, Joon Sig-
dc.contributor.authorChoi, Min Ji-
dc.contributor.authorKo, Kyung Soo-
dc.contributor.authorRhee, Byoung Doo-
dc.contributor.authorPak, Youngmi Kim-
dc.contributor.authorBang, In Seok-
dc.contributor.authorLee, Minhyung-
dc.date.accessioned2022-12-21T10:37:31Z-
dc.date.available2022-12-21T10:37:31Z-
dc.date.created2022-09-16-
dc.date.issued2006-09-
dc.identifier.issn0253-2964-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/181072-
dc.description.abstractIt has been found that a number of diseases are associated with mutations in the mitochondrial DNA. Therapeutic gene delivery to mitochondria has been suggested as a clinical option for these diseases. In this study, we developed a gene carrier to mitochondria by the conjugation of mitochondrial leader peptide (LP) to polyethylenimine (PEI). Mitochondrial LP conjugated PEI (PEI-LP) was synthesized with low molecular weight PEI (2,000 Da, PEI2K). Gel retardation assay showed that PEI2K-LP formed complexes at a 1.0/1 weight ratio. In addition, PEI2K-LP protected DNA from the enzymatic degradation for at least 60 min, while naked DNA was completely degraded within 20 rum. PEI2K-LP was compared with LP conjugated high molecular weight PEI (25,000 Da, PEI25K) in terms of toxicity and delivery efficiency. MTT assay showed that PEI2K-LP had much lower cytotoxicity than PEI25K-LP to 293 cells. In addition, cell-free DNA delivery assay showed that PEI2K-LP delivered more DNA to mitochondria at a 1.8/1 weight ratio than naked DNA or PEI. This result suggests that PEI2K-LP may be useful for the development of mitochondrial gene therapy system with lower cytotoxicity.-
dc.language영어-
dc.language.isoen-
dc.publisherKOREAN CHEMICAL SOC-
dc.titleLow molecular weight polyethylenimine-mitochondrial leader peptide conjugate for DNA delivery to mitochondria-
dc.typeArticle-
dc.contributor.affiliatedAuthorLee, Minhyung-
dc.identifier.doi10.5012/bkcs.2006.27.9.1335-
dc.identifier.scopusid2-s2.0-33749023859-
dc.identifier.wosid000241448300013-
dc.identifier.bibliographicCitationBULLETIN OF THE KOREAN CHEMICAL SOCIETY, v.27, no.9, pp.1335 - 1340-
dc.relation.isPartOfBULLETIN OF THE KOREAN CHEMICAL SOCIETY-
dc.citation.titleBULLETIN OF THE KOREAN CHEMICAL SOCIETY-
dc.citation.volume27-
dc.citation.number9-
dc.citation.startPage1335-
dc.citation.endPage1340-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.identifier.kciidART001192767-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusPLASMID DNA-
dc.subject.keywordPlusGENE DELIVERY-
dc.subject.keywordPlusSEQUENCE-
dc.subject.keywordPlusDISEASES-
dc.subject.keywordPlusLOCALIZATION-
dc.subject.keywordPlusTRANSFECTION-
dc.subject.keywordPlusPROTEOME-
dc.subject.keywordPlusCELLS-
dc.subject.keywordPlusENHANCEMENT-
dc.subject.keywordPlusEFFICIENCY-
dc.subject.keywordAuthorgene delivery-
dc.subject.keywordAuthormitochondria-
dc.subject.keywordAuthorleader peptide-
dc.subject.keywordAuthorpolyethylenimine-
dc.identifier.urlhttp://koreascience.or.kr/article/JAKO200602727181303.page-
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