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在金基底上制备DNA-蛋白质共轭层及其在免疫传感器中的应用。

Fabrication of DNA-protein conjugate layer on gold-substrate and its application to immunosensor.

作者信息

Choi Jeong-Woo, Chun Bum Suk, Oh Byung-Keun, Lee Woochang, Lee Won Hong

机构信息

Department of Chemical and Biomolecular Engineering, Sogang University, Mapo-Gu, Seoul 121 742, Republic of Korea.

出版信息

Colloids Surf B Biointerfaces. 2005 Feb 25;40(3-4):173-7. doi: 10.1016/j.colsurfb.2004.10.020.

Abstract

The fabrication of antibody thin film using both protein G and oligonucleotide was carried out by self-assembly (SA) technique for immunosensor. A mixture of 11-mercaptoundecanoic acid (MUA) and oligonucleotide with thiol (SH) end group was self-assembled of gold (Au) surface for two-dimensional (2D) configuration. Protein G was chemically adsorbed on the 11-MUA surface, and then the antibody was immobilized on the protein G region. On the immobilized single-stranded DNA, the complementary DNA-antibody conjugate was hybridized for the oriented immobilization of antibody. The formation of self-assembled 11-MUA/oligonucleotide layer, protein G immobilization, antibody layer, and antigen binding was investigated using surface plasmon resonance (SPR). The topographies of the fabricated surfaces were observed by atomic force microscopy (AFM). When compared with the amount of antigen binding on the antibody thin film fabricated by protein G only, the proposed biosurface fabricated with both protein G and oligonucleotide showed better binding capacity, which implicates the improvement of the detection limit.

摘要

利用蛋白G和寡核苷酸通过自组装(SA)技术制备用于免疫传感器的抗体薄膜。将11-巯基十一烷酸(MUA)和带有硫醇(SH)端基的寡核苷酸的混合物在金(Au)表面进行自组装,形成二维(2D)结构。蛋白G化学吸附在11-MUA表面,然后将抗体固定在蛋白G区域。在固定的单链DNA上,互补的DNA-抗体缀合物杂交以实现抗体的定向固定。使用表面等离子体共振(SPR)研究自组装的11-MUA/寡核苷酸层的形成、蛋白G固定、抗体层以及抗原结合。通过原子力显微镜(AFM)观察所制备表面的形貌。与仅用蛋白G制备的抗体薄膜上的抗原结合量相比,用蛋白G和寡核苷酸共同制备的生物表面显示出更好的结合能力,这意味着检测限得到了改善。

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