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增强定向固定效率:一种用于食源性病原体高灵敏检测的双生物特异性纳米抗体支架。

Enhancing Oriented Immobilization Efficiency: A One-for-Two Organism-Bispecific Nanobody Scaffold for Highly Sensitive Detection of Foodborne Pathogens.

机构信息

College of Food Science and Engineering, Northwest A&F University, Yangling, Shaanxi 712100, PR China.

College of Life Sciences, Northwest A&F University, Yangling, Shaanxi 712100, PR China.

出版信息

Anal Chem. 2023 Nov 21;95(46):17135-17142. doi: 10.1021/acs.analchem.3c04446. Epub 2023 Nov 8.

Abstract

Nanobodies have gained widespread application in immunoassays. However, their small size presents a significant challenge in achieving effective immobilization and optimal sensitivity. Here, we present a novel "one-for-two"-oriented immobilization platform based on an organism-bispecific nanobody (O-BsNb) scaffold, enabling highly sensitive detection of two bacterial pathogens. Through genetic engineering, a bispecific nanobody (BsNb) was engineered, targeting spp. and . The O-BsNb scaffold allowed one nanobody to bind specifically to inactivated bacteria, forming an organism-oriented immobilization platform, while the other served as the capture antibody. Consequently, the O-BsNb bioscaffold-based ELISA (O-ELISA) for individual detection of and was established. When compared to the sandwich ELISA utilizing passive immobilization of monovalent nanobodies, the O-ELISA exhibited a remarkable 13.4- and 13.7-fold improvement in LOD for and , respectively, highlighting the enhanced immobilization efficacy of the O-ELISA. Furthermore, the feasibility and reproducibility of the assay in practical samples were meticulously evaluated, revealing exemplary performance in terms of recovery precision and assay stability. These findings demonstrate the significant potential of the O-ELISA platform for the sensitive detection of macromolecules, opening new avenues for efficient pathogen identification in foodborne safety and clinical diagnostics.

摘要

纳米抗体在免疫分析中得到了广泛的应用。然而,它们的小尺寸在实现有效的固定化和最佳的灵敏度方面带来了巨大的挑战。在这里,我们提出了一种基于双特异性纳米抗体(BsNb)支架的新型“一分为二”导向固定化平台,用于高灵敏度检测两种细菌病原体。通过基因工程,构建了一种针对 spp.和 的双特异性纳米抗体(BsNb)。O-BsNb 支架允许一个纳米抗体特异性地结合失活的细菌,形成一个面向生物体的固定化平台,而另一个则作为捕获抗体。因此,建立了基于 O-BsNb 生物支架的酶联免疫吸附试验(O-ELISA)用于个体检测 和 。与利用单价纳米抗体被动固定化的夹心 ELISA 相比,O-ELISA 对 和 的 LOD 分别提高了 13.4 倍和 13.7 倍,突出了 O-ELISA 增强的固定化效果。此外,还详细评估了该检测方法在实际样品中的可行性和重现性,在回收率精度和测定稳定性方面表现出优异的性能。这些发现表明 O-ELISA 平台在检测大分子方面具有显著的潜力,为食品安全和临床诊断中的病原体高效鉴定开辟了新的途径。

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