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使用硅标记的蛋白A将抗体定向固定在硅片上。

Oriented immobilization of antibodies on a silicon wafer using Si-tagged protein A.

作者信息

Ikeda Takeshi, Hata Yumehiro, Ninomiya Ken-Ichi, Ikura Yoshiaki, Takeguchi Keigo, Aoyagi Satoka, Hirota Ryuichi, Kuroda Akio

机构信息

Department of Molecular Biotechnology, Graduate School of Advanced Sciences of Matter, Hiroshima University, 1-3-1 Kagamiyama, Higashi-Hiroshima, Hiroshima 739-8530, Japan.

出版信息

Anal Biochem. 2009 Feb 1;385(1):132-7. doi: 10.1016/j.ab.2008.11.001. Epub 2008 Nov 7.

Abstract

We previously reported a silica-binding protein, designated Si-tag, which can be used to immobilize proteins on silica surfaces. Here, we constructed a fusion protein of Si-tag and immunoglobulin-binding staphylococcal protein A for oriented immobilization of antibodies on a silicon wafer whose surface is oxidized to silicon dioxide (silica). The fusion protein, Si-tagged protein A, strongly bound to the silica surface with a dissociation constant of 0.31 nM. Time-of-flight secondary ion mass spectrometry analysis of the silicon wafer coated with Si-tagged protein A, combined with principal component analysis and mutual information, demonstrated that protein A is localized on the outermost surface of the bound protein layer. Immunoglobulin G (IgG) was immobilized both on the silicon wafer coated with Si-tagged protein A and, as a control, directly on the intact silicon wafer via physical adsorption. The silicon wafer coated with Si-tagged protein A bound 30-70% more IgG than the uncoated silicon wafer, whereas the antigen-binding activity was 4- to 5-fold higher for the former, indicating that IgG was functionally immobilized on the silicon wafer via Si-tagged protein A in an oriented manner.

摘要

我们之前报道了一种名为Si-tag的硅结合蛋白,它可用于将蛋白质固定在硅表面。在此,我们构建了一种Si-tag与免疫球蛋白结合性葡萄球菌蛋白A的融合蛋白,用于将抗体定向固定在表面已氧化为二氧化硅(硅石)的硅片上。该融合蛋白,即带有Si-tag的蛋白A,以0.31 nM的解离常数与硅石表面紧密结合。对涂覆有带有Si-tag的蛋白A的硅片进行飞行时间二次离子质谱分析,并结合主成分分析和互信息分析,结果表明蛋白A位于结合蛋白层的最外表面。免疫球蛋白G(IgG)既固定在涂覆有带有Si-tag的蛋白A的硅片上,作为对照,也通过物理吸附直接固定在完整的硅片上。涂覆有带有Si-tag的蛋白A的硅片比未涂覆的硅片结合的IgG多30 - 70%,而前者的抗原结合活性高4至5倍,这表明IgG通过带有Si-tag的蛋白A以定向方式功能性地固定在硅片上。

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