Employing an amphipathic viral peptide to create a lipid bilayer on Au and TiO2

被引:93
作者
Cho, Nam-Joon
Cho, Sang-Joon
Cheong, Kwang Ho
Glenn, Jeffrey S. [1 ]
Frank, Curtis W.
机构
[1] Stanford Univ, Dept Med, Div Gastroenterol & Hepatol, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Chem Engn, Stanford, CA 94305 USA
[3] Pk Syst Corp, Suwon 443766, South Korea
关键词
D O I
10.1021/ja0701412
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Supported lipid bilayers formed by the fusion of small unilamellar vesicles onto SiO2 or organic film-modified surfaces serve as model membranes in both scientific research and practical applications. Here, we describe the use of an amphipathic alpha-helical viral peptide derived from the hepatitis C virus NS5A protein (AH peptide) to destabilize the vesicles leading to lipid bilayer formation on gold and TiO2 solid substrates. Whereas previous researchers have been limited in their selection of surface materials for lipid biomembranes, the use of such peptides as destabilizing agents will allow the freedom to choose a broader variety of solid substrates to support planar bilayers. In particular, the favorable electrical properties of gold and the beneficial biocompatibility of TiO2 make these substrates attractive. The formation of model lipid bilayers supported on gold and TiO2 substrates can be utilized in many membrane-associated biological, physiological, or electrochemical applications with the advantages provided by both of these supporting solid surfaces.
引用
收藏
页码:10050 / +
页数:3
相关论文
共 19 条
  • [1] Penetration and interactions of the antimicrobial peptide, microcin J25, into uncharged phospholipid monolayers
    Bellomio, A
    Oliveira, RG
    Maggio, B
    Morero, RD
    [J]. JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2005, 285 (01) : 118 - 124
  • [2] Amphipathic helix-dependent localization of NS5A mediates hepatitis C virus RNA replication
    Elazar, M
    Cheong, KH
    Liu, P
    Greenberg, HB
    Rice, CM
    Glenn, JS
    [J]. JOURNAL OF VIROLOGY, 2003, 77 (10) : 6055 - 6061
  • [3] Interaction of antimicrobial peptide protegrin with biomembranes
    Gidalevitz, D
    Ishitsuka, YJ
    Muresan, AS
    Konovalov, O
    Waring, AJ
    Lehrer, RI
    Lee, KYC
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (11) : 6302 - 6307
  • [4] ISHITSUKA Y, 2006, UNPUB
  • [5] Kasemo B, 1988, Int J Oral Maxillofac Implants, V3, P247
  • [6] BIOMATERIAL AND IMPLANT SURFACES - ON THE ROLE OF CLEANLINESS, CONTAMINATION, AND PREPARATION PROCEDURES
    KASEMO, B
    LAUSMAA, J
    [J]. JOURNAL OF BIOMEDICAL MATERIALS RESEARCH-APPLIED BIOMATERIALS, 1988, 22 (A2): : 145 - 158
  • [7] Formation of supported membranes from vesicles
    Keller, CA
    Glasmästar, K
    Zhdanov, VP
    Kasemo, B
    [J]. PHYSICAL REVIEW LETTERS, 2000, 84 (23) : 5443 - 5446
  • [8] Surface specific kinetics of lipid vesicle adsorption measured with a quartz crystal microbalance
    Keller, CA
    Kasemo, B
    [J]. BIOPHYSICAL JOURNAL, 1998, 75 (03) : 1397 - 1402
  • [9] Membrane thinning due to antimicrobial peptide binding: An atomic force microscopy study of MSI-78 in lipid bilayers
    Mecke, A
    Lee, DK
    Ramamoorthy, A
    Orr, BG
    Holl, MMB
    [J]. BIOPHYSICAL JOURNAL, 2005, 89 (06) : 4043 - 4050
  • [10] Supported hybrid bilayer membranes as rugged cell membrane mimics
    Plant, AL
    [J]. LANGMUIR, 1999, 15 (15) : 5128 - 5135