Fabrication of protein-anchoring surface by modification of Sio(2) with liposomal bilayer
- Authors
- Cho, Hyung-Min; Cho, Do Youn; Jeon, Jun Yeoung; Hwang, Sang Youn; An, Il Sin; Choo, Jaebum; Lee, Eun-kyu
- Issue Date
- Jan-2010
- Publisher
- Elsevier BV
- Keywords
- Liposome; DPPC; Surface modification; Biofunctionalization; BAM; Protein-anchoring
- Citation
- Colloids and Surfaces B: Biointerfaces, v.75, no.1, pp 209 - 213
- Pages
- 5
- Indexed
- SCI
SCIE
SCOPUS
- Journal Title
- Colloids and Surfaces B: Biointerfaces
- Volume
- 75
- Number
- 1
- Start Page
- 209
- End Page
- 213
- URI
- https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/40036
- DOI
- 10.1016/j.colsurfb.2009.08.033
- ISSN
- 0927-7765
1873-4367
- Abstract
- SiO2 surface was successfully modified with phospholipid bilayer for biocompatibility by covering the planar surface with vesicular liposomes By applying heat to rupture the vesicle, they were converted into a planar form To effectively decorate the bilayer with biological molecules such as a protein, RAM (biological anchor for membrane) was used as a linker. It is a linear assembly consisting of oleyl chain. polyethylene glycol, and NHS (N-hydroxysuccinimide). After a target protein (BSA) was conjugated with RAM by NHS replacement, the conjugate was effectively inserted to the phospholipid bilayer through the lipophilic interaction between the oleyl chain and the lipid bilayer The entire process was monitored and quantitatively analyzed by QCM (quartz crystal microbalance). BSA-BAM conjugate showed approximately 12-fold higher binding efficiency to the lipid bilayer than BSA alone. From this result, we conclude that SiO2 surface could be modified to a lipid bilayer surface so as to anchor a protein by the action of BAM. (C) 2009 Elsevier B V All rights reserved
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