Enhancing membrane modulus of giant unilamellar lipid vesicles by lateral co-assembly of amphiphilic triblock copolymers
- Authors
- Kang, Jeong Yi; Choi, Ikjang; Seo, Mintae; Lee, Jin Yong; Hong, Sungjun; Gong, Gyeonghyeon; Shin, Song Seok; Lee, Youngbok; Kim, 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.
- Files in This Item
-
Go to Link
- Appears in
Collections - COLLEGE OF SCIENCE AND CONVERGENCE TECHNOLOGY > DEPARTMENT OF CHEMICAL AND MOLECULAR ENGINEERING > 1. Journal Articles

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