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利用自粘附抗体结合蛋白制备抗体微孔阵列

Fabrication of an antibody microwell array with self-adhering antibody binding protein.

作者信息

Tanaka Gen, Funabashi Hisakage, Mie Masayasu, Kobatake Eiry

机构信息

Department of Biological Information, Graduate School of Bioscience and Biotechnology, Tokyo Institute of Technology, 4259 Nagatsuta-cho, Midori-ku, Yokohama 226-8501, Japan.

出版信息

Anal Biochem. 2006 Mar 15;350(2):298-303. doi: 10.1016/j.ab.2005.12.034. Epub 2006 Jan 17.

Abstract

One of the promising methods of preparing antibody arrays is immobilizing antibodies with protein A or protein G, each of which binds specifically to the heavy chain constant (Fc) region of immunoglobulin G (IgG). In this system, antibody immobilization efficiency depends on the number of active Fc binding proteins that need to be immobilized on the surface. Here we have designed and constructed an Fc binding protein with a self-adhering ability that can be immobilized on the hydrophobic surface by simple adsorption. It consists of an Fc binding domain of protein G (G3) and hydrophobic domain of elastin (E72). Direct observation revealed its self-adhering ability on the hydrophobic surface. The enzyme-linked immunosorbent assay (ELISA) showed that it retained antibody binding ability on the surface. The antibody array model was prepared on a hydrophobic microwell glass slide with E72G3, which specifically detect the antigen with a sevenfold greater sensitivity than the G3-treated slide. These results suggest that the E72G3 is useful for simple and effective immobilization of antibodies and can be used to fabricate any immuno devices.

摘要

制备抗体阵列的一种有前景的方法是用蛋白A或蛋白G固定抗体,蛋白A和蛋白G均可特异性结合免疫球蛋白G(IgG)的重链恒定区(Fc)。在该系统中,抗体固定效率取决于需要固定在表面的活性Fc结合蛋白的数量。在此,我们设计并构建了一种具有自粘附能力的Fc结合蛋白,它可以通过简单吸附固定在疏水表面。它由蛋白G的Fc结合结构域(G3)和弹性蛋白的疏水结构域(E72)组成。直接观察揭示了其在疏水表面的自粘附能力。酶联免疫吸附测定(ELISA)表明它在表面保留了抗体结合能力。用E72G3在疏水微孔玻璃载玻片上制备了抗体阵列模型,其检测抗原的灵敏度比G3处理的载玻片高7倍。这些结果表明,E72G3可用于简单有效地固定抗体,并可用于制造任何免疫装置。

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