Combination Screening of a Naïve Antibody Library Using E. coli Display and Single-Step Colony Assay

Mieko Kato, Y. Hanyu
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Abstract

The use of single-domain camelid antibodies, termed VHHs or nanobodies, has found increasing application in diagnosis, pharmaceutical development, and research because of their superior properties, such as small size, elevated stability, high water solubility, and excellent affinity for the antigen. Antigen-specific VHHs are generated by screening VHH display libraries via bio-panning. However, the bio-panning step needs to be repeated multiple times, which is time-consuming and laborious. Here, we developed a simple and rapid screening method that combined Escherichia coli display and a single-step colony assay to successfully identify positive clones from a naïve VHH library. The library was constructed from peripheral blood mononuclear cells of alpaca, and VHHs were displayed on the surface of E. coli using the inverse autotransporter intimin. Libraries enriched by magnetic cell sorting were screened directly using a single-step colony assay. Colonies formed on the hydrophilic filter and antigen-coated membrane. The expression of VHHs was induced, and those bound to the antigen on the membrane were detected as positive clones. Screening and identification of positive clones required only two days, which saves considerable time and resources compared to existing protocols.
利用大肠杆菌展示和单步菌落检测组合筛选原始抗体库
单域驼科抗体被称为 VHH 或纳米抗体,由于其具有体积小、稳定性高、水溶性强以及与抗原亲和力强等优越性能,在诊断、药物开发和研究领域的应用日益广泛。抗原特异性 VHH 是通过生物平移筛选 VHH 显示库产生的。然而,生物筛选步骤需要重复多次,费时费力。在此,我们开发了一种简单而快速的筛选方法,它结合了大肠杆菌展示和单步菌落检测法,能成功地从幼稚 VHH 文库中鉴定出阳性克隆。文库是由羊驼的外周血单核细胞构建的,并利用反向自转运蛋白将 VHH 显示在大肠杆菌表面。通过磁性细胞分选富集的文库直接使用单步菌落检测法进行筛选。菌落在亲水过滤器和抗原包被膜上形成。诱导 VHHs 表达,与膜上抗原结合的 VHHs 被检测为阳性克隆。筛选和鉴定阳性克隆只需两天时间,与现有方案相比节省了大量时间和资源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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