Human Health Therapeutics Research Centre, National Research Council Canada, Ottawa, ON, Canada.
Department of Biochemistry, Microbiology and Immunology, University of Ottawa, Ottawa, ON, Canada.
Methods Mol Biol. 2023;2702:489-540. doi: 10.1007/978-1-0716-3381-6_26.
Next-generation DNA sequencing (NGS) technologies have made it possible to interrogate antibody repertoires to unprecedented depths, typically via sequencing of cDNAs encoding immunoglobulin variable domains. In the absence of heavy-light chain pairing, the variable domains of heavy chain-only antibodies (HCAbs), referred to as single-domain antibodies (sdAbs), are uniquely amenable to NGS analyses. In this chapter, we provide simple and rapid protocols for producing and sequencing multiplexed immunoglobulin variable domain (VH, V or V) amplicons derived from a variety of sources using the Illumina MiSeq platform. Generation of such amplicon libraries is relatively inexpensive, requiring no specialized equipment and only a limited set of PCR primers. We also present several applications of NGS to sdAb discovery and engineering, including: (1) evaluation of phage-displayed sdAb library sequence diversity and monitoring of panning experiments; (2) identification of sdAbs of predetermined epitope specificity following competitive elution of phage-displayed sdAb libraries; (3) direct selection of B cells expressing antigen-specific, membrane-bound HCAb using antigen-coupled magnetic beads and identification of antigen-specific sdAbs, and (4) affinity maturation of lead sdAbs using tandem phage display selection and NGS. These methods can easily be adapted to other types of proteins and libraries and expand the utility of in vitro display technology.
下一代 DNA 测序(NGS)技术使得对抗体库进行前所未有的深度分析成为可能,通常是通过对编码免疫球蛋白可变区的 cDNA 进行测序。在没有重链-轻链配对的情况下,仅重链抗体(HCAb)的可变区,称为单域抗体(sdAb),非常适合 NGS 分析。在本章中,我们提供了简单而快速的方案,使用 Illumina MiSeq 平台,从各种来源生成和测序多重免疫球蛋白可变区(VH、V 或 V)扩增子。这种扩增子文库的生成相对便宜,不需要特殊设备,只需一组有限的 PCR 引物。我们还介绍了 NGS 在 sdAb 发现和工程中的几个应用,包括:(1)评估噬菌体展示 sdAb 文库的序列多样性和监测淘选实验;(2)在竞争洗脱噬菌体展示 sdAb 文库后,鉴定具有预定表位特异性的 sdAb;(3)使用抗原偶联磁珠直接选择表达抗原特异性、膜结合 HCAb 的 B 细胞,并鉴定抗原特异性 sdAb;(4)使用串联噬菌体展示选择和 NGS 对先导 sdAb 进行亲和力成熟。这些方法可以很容易地适应其他类型的蛋白质和文库,并扩大体外展示技术的应用。