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用于纳米银表面免疫标记的金/银核壳纳米颗粒上的可控蛋白质包埋。

Controlled protein embedment onto Au/Ag core-shell nanoparticles for immuno-labeling of nanosilver surface.

作者信息

Lee In Hwan, Lee Jeong Min, Jung Yongwon

机构信息

Department of Chemistry, Korea Advanced Institute of Science and Technology , Daejeon 305-701, Korea.

出版信息

ACS Appl Mater Interfaces. 2014 May 28;6(10):7659-64. doi: 10.1021/am500960b. Epub 2014 May 15.

DOI:10.1021/am500960b
PMID:24801432
Abstract

Difficulties in stable conjugation of biomolecules to nanosilver surfaces have severely limited the use of silver nanostructures in biological applications. Here, we report a facile antibody conjugation onto gold/silver (Au/Ag) core-shell nanoparticles by stable and uniform embedment of an antibody binding protein, protein G, in silver nanoshells. A rigid helical peptide linker with a terminal cysteine residue was fused to protein G. A mixture of the peptide-fused protein G and space-filling free peptide was reacted with gold nanoparticles (AuNPs) to form a protein G-linked peptide layer on the particle surface. Uniform silver nanoshells were successfully formed on these protein G-AuNPs, while stably embedding protein G-linked peptide layers. Protein G specifically targets the Fc region of an antibody and thus affords properly orientated antibodies on the particle surface. Compared to Au nanoparticles of similar size with randomly adsorbed antibodies, the present immuno-labeled Au/Ag core-shell nanoparticles offered nearly 10-fold higher sensitivities for naked-eye detection of surface bound antigens. In addition, small dye molecules that were bonded to the peptide layer on Au nanoparticles exhibited highly enhanced surface-enhanced Raman scattering (SERS) signals upon Ag shell formation. The present strategy provides a simple but efficient way to conjugate antibodies to nanosilver surfaces, which will greatly facilitate wider use of the superior optical properties of silver nanostructures in biological applications.

摘要

生物分子与纳米银表面的稳定结合存在困难,这严重限制了银纳米结构在生物应用中的使用。在此,我们报告了一种通过将抗体结合蛋白G稳定且均匀地嵌入银纳米壳中,将抗体轻松结合到金/银(Au/Ag)核壳纳米颗粒上的方法。将带有末端半胱氨酸残基的刚性螺旋肽接头与蛋白G融合。将肽融合蛋白G和填充空间的游离肽的混合物与金纳米颗粒(AuNPs)反应,在颗粒表面形成蛋白G连接的肽层。在这些蛋白G-AuNPs上成功形成了均匀的银纳米壳,同时稳定地嵌入了蛋白G连接的肽层。蛋白G特异性靶向抗体的Fc区域,从而在颗粒表面提供正确定向的抗体。与具有随机吸附抗体的类似尺寸的金纳米颗粒相比,目前的免疫标记Au/Ag核壳纳米颗粒对表面结合抗原的肉眼检测灵敏度提高了近10倍。此外,与金纳米颗粒上的肽层结合的小染料分子在形成银壳后表现出高度增强的表面增强拉曼散射(SERS)信号。本策略提供了一种将抗体结合到纳米银表面的简单而有效的方法,这将极大地促进银纳米结构优异光学性质在生物应用中的更广泛使用。

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