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Direct Immobilization of Gold-Binding Antibody Fragments for Immunosensor Applications

机译:直接固定金结合抗体片段在免疫传感器中的应用

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摘要

A novel method that enables antibody fragments to be immobilized on a sensor substrate with a high binding capability using molecular recognition has been developed. Using genetic engineering, we fabricated bispecific recombinant antibody fragments, which consist of two kinds of antibody fragments: a gold antibody fragment and a target molecule antibody fragment. Surface plasmon resonance (SPR) analysis indicated that these gold-binding bispecific antibody fragments bind directly to the gold substrate with high affinity (K_(D) approx 10~(-9) M). About 70percent of the bispecific antibody fragments immobilized on the gold substrate retained their target protein-binding efficiency. The Sips isotherm was used to assess the heterogeneity in antibody affinity for the bispecific antibody fragments. The results showed that the immobilized bispecific antibody fragments exhibited an increased homogeneity of affinity (K_(D)) to target molecules when compared with monospecific antibody fragments immobilized by conventional methods. The use of bispecific antibody fragments to directly immobilize antibody fragments on a solid-phase substrate offers a useful platform for immunosensor applications.
机译:已经开发出一种新颖的方法,该方法能够使用分子识别将抗体片段以高结合能力固定在传感器基板上。通过基因工程,我们制备了双特异性重组抗体片段,该片段由两种抗体片段组成:金抗体片段和靶分子抗体片段。表面等离子体共振(SPR)分析表明,这些结合金的双特异性抗体片段以高亲和力(K_(D)约10〜(-9)M)直接结合到金底物上。固定在金底物上的双特异性抗体片段中约有70%保留了其靶蛋白结合效率。 Sips等温线用于评估双特异性抗体片段的抗体亲和力的异质性。结果显示,与通过常规方法固定的单特异性抗体片段相比,固定的双特异性抗体片段显示出对靶分子的亲和力(K_(D))的均一性提高。使用双特异性抗体片段将抗体片段直接固定在固相底物上为免疫传感器应用提供了有用的平台。

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