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Enhancing membrane modulus of giant unilamellar lipid vesicles by lateral co-assembly of amphiphilic triblock copolymers

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dc.contributor.authorKang, Jeong Yi-
dc.contributor.authorChoi, Ikjang-
dc.contributor.authorSeo, Mintae-
dc.contributor.authorLee, Jin Yong-
dc.contributor.authorHong, Sungjun-
dc.contributor.authorGong, Gyeonghyeon-
dc.contributor.authorShin, Song Seok-
dc.contributor.authorLee, Youngbok-
dc.contributor.authorKim, Jin Woong-
dc.date.accessioned2021-06-22T09:07:02Z-
dc.date.available2021-06-22T09:07:02Z-
dc.date.issued2020-03-
dc.identifier.issn0021-9797-
dc.identifier.issn1095-7103-
dc.identifier.urihttps://scholarworks.bwise.kr/erica/handle/2021.sw.erica/1224-
dc.description.abstractWe report a facile, but robust approach to fabricate structurally stable giant unilamellar vesicles (GUVs), on which a 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) bilayer membrane was made rigid by introducing amphiphilic block polymers. Particularly, we found that lateral co-assembly of an amphiphilic triblock copolymer (ATC) structured with a hydrophobic middle block and long molecular weight (20 K g/mol) hydrophilic end blocks remarkably enhanced the stretching modulus (k) of GUVs. When the membrane composition was optimized, the k value of ATC-hybridized GUVs increased to 6.2 x 10(8) Pa, which was approximately 10-fold higher than that of DPPC GUVs, thus leading to a much longer half-life. Moreover, we demonstrated that our ATC-hybridized GUVs enabled development of a fascinating vesicular model, which shows great potential as a structurally stable cell membrane mimic. (C) 2019 Elsevier Inc. All rights reserved.-
dc.format.extent9-
dc.language영어-
dc.language.isoENG-
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCE-
dc.titleEnhancing membrane modulus of giant unilamellar lipid vesicles by lateral co-assembly of amphiphilic triblock copolymers-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1016/j.jcis.2019.10.109-
dc.identifier.scopusid2-s2.0-85075445112-
dc.identifier.wosid000508752600030-
dc.identifier.bibliographicCitationJOURNAL OF COLLOID AND INTERFACE SCIENCE, v.561, pp 318 - 326-
dc.citation.titleJOURNAL OF COLLOID AND INTERFACE SCIENCE-
dc.citation.volume561-
dc.citation.startPage318-
dc.citation.endPage326-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.subject.keywordPlusBLOCK-COPOLYMERS-
dc.subject.keywordPlusCELLULAR UPTAKE-
dc.subject.keywordPlusGENE DELIVERY-
dc.subject.keywordPlusNOESY NMR-
dc.subject.keywordPlusPOLYMERSOME-
dc.subject.keywordPlusENCAPSULATION-
dc.subject.keywordPlusSTABILITY-
dc.subject.keywordPlusDIFFUSION-
dc.subject.keywordPlusRELEASE-
dc.subject.keywordPlusPEPTIDE-
dc.subject.keywordAuthorGiant unilamellar vesicles-
dc.subject.keywordAuthorBlock copolymers-
dc.subject.keywordAuthorLateral co-assembly-
dc.subject.keywordAuthorMembrane modulus-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S0021979719312962?via%3Dihub-
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