DC Field | Value | Language |
---|---|---|
dc.contributor.author | Kim, SJ | - |
dc.contributor.author | Bang, EK | - |
dc.contributor.author | Kwon, HJ | - |
dc.contributor.author | Shim, JS | - |
dc.contributor.author | Kim, BH | - |
dc.date.accessioned | 2016-04-01T02:19:44Z | - |
dc.date.available | 2016-04-01T02:19:44Z | - |
dc.date.created | 2009-02-28 | - |
dc.date.issued | 2004-11-05 | - |
dc.identifier.issn | 1439-4227 | - |
dc.identifier.other | 2004-OAK-0000004678 | - |
dc.identifier.uri | https://oasis.postech.ac.kr/handle/2014.oak/24925 | - |
dc.description.abstract | Their enhanced cell permeability and their ability to mimic DNA structures make modified oligodeoxyribonucleotides (ODNs) very important substances for increasing our understanding of cell biology and for therapeutic applications. Lithocholic acid is a hydrophobic secondary bile acid that is a substrate of nuclear Pregnane X receptor (PXR). We designed and synthesized novel lithocholic acid-based ODNs (L-ODNs) by using a new phosphoramidite derived from lithocholic acid. By comparing data obtained from circular-dichroism, melting-point, and theoretical studies, we believe that these L-ODNs adopt DNA hairpin structures. Furthermore, L-ODNs have enhanced cellular uptake properties with respect to regular ODNs. To demonstrate their enhanced cell permeabilites, we carried out cellular uptake experiments of L-ODNs in HeLa cells. By attaching fluorescein as a fluorescence label and using confocal microscopy, we observed that the permeability of L-ODNs is much higher that that of natural ODNs. | - |
dc.description.statementofresponsibility | X | - |
dc.language | English | - |
dc.publisher | WILEY-V C H VERLAG GMBH | - |
dc.relation.isPartOf | CHEMBIOCHEM | - |
dc.subject | SYNTHETIC DNA HAIRPINS | - |
dc.subject | TRIPLE-HELIX FORMATION | - |
dc.subject | RECEPTOR PXR | - |
dc.subject | OLIGODEOXYNUCLEOTIDES | - |
dc.subject | HYBRIDIZATION | - |
dc.subject | REPLICATION | - |
dc.subject | NUCLEOSIDES | - |
dc.subject | DYNAMICS | - |
dc.subject | HYBRIDS | - |
dc.subject | STRAND | - |
dc.title | Modified oligonucleotides containing lithocholic acid in their backbones: Their enhanced cellular uptake and their mimicking of hairpin structures | - |
dc.type | Article | - |
dc.contributor.college | 화학과 | - |
dc.identifier.doi | 10.1002/CBIC.2004001 | - |
dc.author.google | Kim, SJ | - |
dc.author.google | Bang, EK | - |
dc.author.google | Kwon, HJ | - |
dc.author.google | Shim, JS | - |
dc.author.google | Kim, BH | - |
dc.relation.volume | 5 | - |
dc.relation.issue | 11 | - |
dc.relation.startpage | 1517 | - |
dc.relation.lastpage | 1522 | - |
dc.contributor.id | 10142056 | - |
dc.relation.journal | CHEMBIOCHEM | - |
dc.relation.index | SCI급, SCOPUS 등재논문 | - |
dc.relation.sci | SCI | - |
dc.collections.name | Journal Papers | - |
dc.type.rims | ART | - |
dc.identifier.bibliographicCitation | CHEMBIOCHEM, v.5, no.11, pp.1517 - 1522 | - |
dc.identifier.wosid | 000225116400006 | - |
dc.date.tcdate | 2019-02-01 | - |
dc.citation.endPage | 1522 | - |
dc.citation.number | 11 | - |
dc.citation.startPage | 1517 | - |
dc.citation.title | CHEMBIOCHEM | - |
dc.citation.volume | 5 | - |
dc.contributor.affiliatedAuthor | Kim, BH | - |
dc.description.journalClass | 1 | - |
dc.description.journalClass | 1 | - |
dc.description.wostc | 19 | - |
dc.type.docType | Article | - |
dc.subject.keywordPlus | SYNTHETIC DNA HAIRPINS | - |
dc.subject.keywordPlus | TRIPLE-HELIX FORMATION | - |
dc.subject.keywordPlus | RECEPTOR PXR | - |
dc.subject.keywordPlus | OLIGODEOXYNUCLEOTIDES | - |
dc.subject.keywordPlus | HYBRIDIZATION | - |
dc.subject.keywordPlus | REPLICATION | - |
dc.subject.keywordPlus | NUCLEOSIDES | - |
dc.subject.keywordPlus | DYNAMICS | - |
dc.subject.keywordPlus | HYBRIDS | - |
dc.subject.keywordPlus | STRAND | - |
dc.relation.journalWebOfScienceCategory | Biochemistry & Molecular Biology | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Medicinal | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Biochemistry & Molecular Biology | - |
dc.relation.journalResearchArea | Pharmacology & Pharmacy | - |
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