Supported Lipid Bilayers on Biocompatible Polysaccharide Multilayers

被引:31
|
作者
Mulligan, Kirk [1 ,2 ]
Jakubek, Zygmunt J. [1 ]
Johnston, Linda J. [1 ,2 ]
机构
[1] Natl Res Council Canada, Steacie Inst Mol Sci, Ottawa, ON K1A 0R6, Canada
[2] Univ Ottawa, Dept Chem, Ottawa, ON KIN 6N5, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
ATOMIC-FORCE MICROSCOPY; PHOSPHOLIPID-BILAYERS; EXPONENTIAL-GROWTH; POLYMER CUSHION; MEMBRANES; SURFACE; CHITOSAN; FILMS; SPECTROSCOPY; HYALURONAN;
D O I
10.1021/la203207p
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Formation of supported lipid bilayers on soft polymer cushions is a useful approach to decouple the membrane from the substrate for applications involving membrane proteins. We prepared biocompatible polymer cushions by the layer-by-layer assembly of two polysaccharide polyelectrolytes, chitosan (CHI) and hyaluronic acid, on glass and silicon substrates. (CHI/FIA)(5) films were characterized by atomic force microscopy, giving an average thickness of 57 nm and roughness of 25 nm in aqueous solution at pH 6.5. Formation of zwitterionic lipid bilayers by the vesicle fusion method was attempted using DOPC vesicles at pH 4 and 6.5 on (CHI/HA)(5) films. At higher pH adsorbed lipids had low mobility and large immobile lipid fractions; a combination of fluorescence and AFM indicated that this was attributable to formation of poor quality membranes with defects and pinned lipids rather than to a layer of surface-adsorbed vesicles. By contrast, more uniform bilayers with mobile lipids were produced at pH 4. Fluorescence recovery after photobleaching gave diffusion coefficients that were similar to those for bilayers on PEG cushions and considerably higher than those measured on other polyelectrolyte films. The results suggest that the polymer surface charge is more important than the surface roughness in controlling formation of mobile supported bilayers. These results demonstrate that polysaccharides provide a useful alternative to other polymer cushions, particularly for applications where biocompatibility is important.
引用
收藏
页码:14352 / 14359
页数:8
相关论文
共 50 条
  • [1] Supported Lipid Bilayers on Biocompatible Polysaccharide Multilayers
    Johnston, Linda J.
    Mulligan, Kirk
    Jakubek, Zygmunt J.
    BIOPHYSICAL JOURNAL, 2012, 102 (03) : 425A - 425A
  • [2] Interfacial and structural characteristics of polyelectrolyte multilayers used as cushions for supported lipid bilayers
    Wlodek, M.
    Kolasinska-Sojka, M.
    Wasilewska, M.
    Bikondoa, O.
    Briscoe, W. H.
    Warszynski, P.
    SOFT MATTER, 2017, 13 (43) : 7848 - 7855
  • [3] Effects of valinomycin doping on the electrical and structural properties of planar lipid bilayers supported on polyelectrolyte multilayers
    Gutierrez-Pineda, Eduart
    Andreozzi, Patrizia
    Diamanti, Eleftheria
    Anguiano, Ramiro
    Ziolo, Ronald F.
    Moya, Sergio E.
    Rodriguez-Presa, Maria Jose
    Gervasi, Claudio A.
    BIOELECTROCHEMISTRY, 2021, 138
  • [4] Lipid and protein separation in supported lipid bilayers
    Liu, Chunming
    Monson, Christopher
    Pace, Hudson
    Cremer, Paul
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2011, 242
  • [5] Protein interactions on supported lipid bilayers
    Cremer, Paul S.
    Daniel, Susan
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2007, 233
  • [6] Dynamical Heterogeneity in Supported Lipid Bilayers
    Liangfang Zhang
    Steve Granick
    MRS Bulletin, 2006, 31 : 527 - 531
  • [7] Nanomechanical properties of supported lipid bilayers
    Zou, Shan
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2011, 241
  • [8] Lipid peroxidation in diamond supported bilayers
    Moreno, A. R. Ortiz
    Li, R.
    Wu, K.
    Schirhagl, R.
    NANOSCALE, 2023, 15 (17) : 7920 - 7928
  • [9] Hypersonic poration of supported lipid bilayers
    Lu, Yao
    Huskens, Jurriaan
    Pang, Wei
    Duan, Xuexin
    MATERIALS CHEMISTRY FRONTIERS, 2019, 3 (05) : 782 - 790
  • [10] Polydopamine-Supported Lipid Bilayers
    Nirasay, Souryvanh
    Badia, Antonella
    Leclair, Gregoire
    Claverie, Jerome P.
    Marcotte, Isabelle
    MATERIALS, 2012, 5 (12) : 2621 - 2636