Full metadata record

DC Field Value Language
dc.contributor.authorPark, Eun Young-
dc.contributor.authorJang, Mihue-
dc.contributor.authorKim, Jong Hwan-
dc.contributor.authorAhn, Hyung Jun-
dc.date.accessioned2024-01-20T08:32:17Z-
dc.date.available2024-01-20T08:32:17Z-
dc.date.created2022-01-10-
dc.date.issued2014-11-
dc.identifier.issn1742-7061-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/126155-
dc.description.abstractIn nature, there exist a wide range of dsRNA-binding proteins that have different binding modes for small interfering RNA (siRNA) as well as structural differences, and some of these proteins have potential as effective siRNA delivery carriers. In order to deliver siRNA into cancer cells, a dsRNA-binding 2b protein derived from Tomato aspermy virus was genetically modified by fusing the integrin-targeting RGD peptide to its C-terminus, and biosynthesized. The resulting 2b-RGD protein possesses distinct characteristics favorable for biomedical applications of siRNA: (i) high affinity for siRNA, (ii) siRNA protection against RNases in serum, (iii) low cytotoxicity compared to the polycationic polymers often employed in conventional siRNA carriers, (iv) specific binding to integrins on cancer cells, and the ability to pass through the cell membrane via endocytosis, and (v) the ability to facilitate cytosolic release of siRNA. Here, we demonstrate that the 2b-RGD/siRNA complexes have great potential as a tumor-targeting siRNA delivery carrier and suggest their possible therapeutic applications for cancer treatment. (C) 2014 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.-
dc.languageEnglish-
dc.publisherELSEVIER SCI LTD-
dc.subjectRNA-SILENCING SUPPRESSION-
dc.subjectCHIMERIC CAPSID PROTEIN-
dc.subjectANTIVIRAL IMMUNITY-
dc.subjectBINDING DOMAIN-
dc.subjectGENE DELIVERY-
dc.subjectEFFICIENT-
dc.subjectINTERFERENCE-
dc.subjectINTEGRIN-
dc.subjectCELLS-
dc.titleGenetically modified Tomato aspermy virus 2b protein as a tumor-targeting siRNA delivery carrier-
dc.typeArticle-
dc.identifier.doi10.1016/j.actbio.2014.07.014-
dc.description.journalClass1-
dc.identifier.bibliographicCitationACTA BIOMATERIALIA, v.10, no.11, pp.4778 - 4786-
dc.citation.titleACTA BIOMATERIALIA-
dc.citation.volume10-
dc.citation.number11-
dc.citation.startPage4778-
dc.citation.endPage4786-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000343854400024-
dc.identifier.scopusid2-s2.0-84908143741-
dc.relation.journalWebOfScienceCategoryEngineering, Biomedical-
dc.relation.journalWebOfScienceCategoryMaterials Science, Biomaterials-
dc.relation.journalResearchAreaEngineering-
dc.relation.journalResearchAreaMaterials Science-
dc.type.docTypeArticle-
dc.subject.keywordPlusRNA-SILENCING SUPPRESSION-
dc.subject.keywordPlusCHIMERIC CAPSID PROTEIN-
dc.subject.keywordPlusANTIVIRAL IMMUNITY-
dc.subject.keywordPlusBINDING DOMAIN-
dc.subject.keywordPlusGENE DELIVERY-
dc.subject.keywordPlusEFFICIENT-
dc.subject.keywordPlusINTERFERENCE-
dc.subject.keywordPlusINTEGRIN-
dc.subject.keywordPlusCELLS-
dc.subject.keywordAuthorRNAi-
dc.subject.keywordAuthorsiRNA delivery carrier-
dc.subject.keywordAuthorTumor-targeting-
dc.subject.keywordAuthorCancer treatment-
dc.subject.keywordAuthorRecombinant proteins-
Appears in Collections:
KIST Article > 2014
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

BROWSE