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

Authors
Kang, Jeong YiChoi, IkjangSeo, MintaeLee, Jin YongHong, SungjunGong, GyeonghyeonShin, Song SeokLee, YoungbokKim, Jin Woong
Issue Date
Mar-2020
Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
Keywords
Giant unilamellar vesicles; Block copolymers; Lateral co-assembly; Membrane modulus
Citation
JOURNAL OF COLLOID AND INTERFACE SCIENCE, v.561, pp 318 - 326
Pages
9
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF COLLOID AND INTERFACE SCIENCE
Volume
561
Start Page
318
End Page
326
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/1224
DOI
10.1016/j.jcis.2019.10.109
ISSN
0021-9797
1095-7103
Abstract
We 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.
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