Meng Yanli, Chen Bo
Changchun Institute of Optics, Fine Mechanics and Physics, Changchun 130033, China.
Annu Int Conf IEEE Eng Med Biol Soc. 2009;2009:1497-500. doi: 10.1109/IEMBS.2009.5334162.
Imaging ellipsometry biosensor was developed on the basement of imaging ellipsometry for thin-film and surface characterization. Using protein A to immobilize Human IgG on silicon surface for the imaging ellipsometry biosensor immunoassay was studied. As a result, The Human IgG immobilized on silicon surface by protein A bound much more polyclonal antibody than that on hydrophobic surface directly, which indicated that protein A could be used to immobilize Human IgG molecules in a highly oriented manner and Human IgG molecule could maintain its native configuration well on the silicon surface. Furthermore, the absorption quantity of Protein A affecting on interaction of Human IgG and antibody molecules was investigated. The surface concentration of Human IgG and antibody molecules was enhanced as well as the increasing of the absorption quantity of Protein A, but there are no obvious increase when the ratio of surface concentration of Protein A layer to that of saturated adsorption is larger than 80%. However, even decrease slightly.
成像椭偏生物传感器是在用于薄膜和表面表征的成像椭偏技术基础上开发的。研究了使用蛋白A将人免疫球蛋白(Human IgG)固定在硅表面用于成像椭偏生物传感器免疫分析。结果表明,通过蛋白A固定在硅表面的人免疫球蛋白比直接固定在疏水表面的人免疫球蛋白结合了更多的多克隆抗体,这表明蛋白A可用于以高度定向的方式固定人免疫球蛋白分子,并且人免疫球蛋白分子在硅表面能够很好地保持其天然构象。此外,研究了蛋白A的吸附量对人免疫球蛋白与抗体分子相互作用的影响。随着蛋白A吸附量的增加,人免疫球蛋白和抗体分子的表面浓度升高,但当蛋白A层的表面浓度与饱和吸附表面浓度之比大于80%时,表面浓度没有明显增加,甚至略有下降。