Oriented immobilization of immunoglobulin G onto the cuvette surface of the resonant mirror biosensor through layer-by-layer assembly of multilayer films

被引:14
作者
Wu, Bao-Yan [1 ]
Hou, Shi-Hua [2 ]
Huang, Liang [1 ]
Yin, Feng [1 ]
Zhao, Zi-Xia [1 ]
Anzai, Jun-Ichi [3 ]
Chen, Qiang [1 ]
机构
[1] Nankai Univ, Coll Life Sci, Key Lab Bioact Mat Minist Educ, Tianjin 300071, Peoples R China
[2] S China Univ Technol, Sch Phys Sci & Technol, Guangzhou 510640, Peoples R China
[3] Tohoku Univ, Grad Sch Pharmaceut Sci, Aoba Ku, Sendai, Miyagi 9808578, Japan
来源
MATERIALS SCIENCE & ENGINEERING C-BIOMIMETIC AND SUPRAMOLECULAR SYSTEMS | 2008年 / 28卷 / 07期
基金
美国国家科学基金会;
关键词
oriented immobilization; resonant mirror biosensor; immunoglobulin G; gold nanoparticles; protein A;
D O I
10.1016/j.msec.2007.04.035
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
A new method for oriented immobilization of immunoglobulin G (IgG) onto the cuvette surface of the resonant mirror biosensor through layer-by-layer (LBL) assembly of multilayer films composed of avidin/gold nanoparticles (GNp)/protein A/IgG was developed. First, avidin was added in the biotin cuvette, and then injected GNp, followed by the injection of protein A for oriented immobilization of IgG. The rinsing with PBS was applied at the end of each assembly deposition for dissociating the weak adsorption. Second, IgG was added in the protein A-coated cuvette, and regenerated by incubation with 0.1 M glycine-HCL buffer. Third, different concentrations of IgG were measured by repeating the second process. Film assembling and properties of the interaction between protein A and IgG were studied by resonant mirror biosensor and electrochemical measurements. Results confirmed that IgG was successfully oriented on the protein A-coated cuvette Surface by LBL assembly of multilayer films. The interaction response was dose-dependent which showed a linear range of 0.1 - 1.6 g L-1 IgG, with a detection limit of 8.7 mg L-1 estimated at a signal-to-noise ratio of 3. Moreover, the assay for oriented immobilization of IgG exhibited a good reproducibility and a favorable reusability. This method can provide a promising platform for fabricating immunoassay and immunosensor systems, protein reactors or protein-modified substrates, and affinity probes. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:1065 / 1069
页数:5
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