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通过基于微流控技术的单病原体特异性抗体分泌细胞荧光激活细胞分选术快速发现单克隆抗体。

Rapid discovery of monoclonal antibodies by microfluidics-enabled FACS of single pathogen-specific antibody-secreting cells.

作者信息

Fischer Katrin, Lulla Aleksei, So Tsz Y, Pereyra-Gerber Pehuén, Raybould Matthew I J, Kohler Timo N, Yam-Puc Juan Carlos, Kaminski Tomasz S, Hughes Robert, Pyeatt Gwendolyn L, Leiss-Maier Florian, Brear Paul, Matheson Nicholas J, Deane Charlotte M, Hyvönen Marko, Thaventhiran James E D, Hollfelder Florian

机构信息

Department of Biochemistry, University of Cambridge, Cambridge, UK.

MRC Toxicology Unit, Gleeson Building, Cambridge, UK.

出版信息

Nat Biotechnol. 2024 Aug 14. doi: 10.1038/s41587-024-02346-5.

Abstract

Monoclonal antibodies are increasingly used to prevent and treat viral infections and are pivotal in pandemic response efforts. Antibody-secreting cells (ASCs; plasma cells and plasmablasts) are an excellent source of high-affinity antibodies with therapeutic potential. Current methods to study antigen-specific ASCs either have low throughput, require expensive and labor-intensive screening or are technically demanding and therefore not widely accessible. Here we present a straightforward technology for the rapid discovery of monoclonal antibodies from ASCs. Our approach combines microfluidic encapsulation of single cells into an antibody capture hydrogel with antigen bait sorting by conventional flow cytometry. With our technology, we screened millions of mouse and human ASCs and obtained monoclonal antibodies against severe acute respiratory syndrome coronavirus 2 with high affinity (<1 pM) and neutralizing capacity (<100 ng ml) in 2 weeks with a high hit rate (>85% of characterized antibodies bound the target). By facilitating access to the underexplored ASC compartment, the approach enables efficient antibody discovery and immunological studies into the generation of protective antibodies.

摘要

单克隆抗体越来越多地用于预防和治疗病毒感染,在应对大流行的工作中起着关键作用。分泌抗体的细胞(ASC;浆细胞和浆母细胞)是具有治疗潜力的高亲和力抗体的极佳来源。目前研究抗原特异性ASC的方法要么通量低,需要昂贵且耗费人力的筛选,要么技术要求高,因此无法广泛应用。在此,我们展示了一种从ASC快速发现单克隆抗体的简便技术。我们的方法将单细胞微流控封装到抗体捕获水凝胶中,并通过传统流式细胞术进行抗原诱饵分选。利用我们的技术,我们筛选了数百万个小鼠和人类ASC,并在两周内获得了针对严重急性呼吸综合征冠状病毒2的具有高亲和力(<1 pM)和中和能力(<100 ng/ml)的单克隆抗体,命中率很高(>85%的鉴定抗体与靶标结合)。通过便于进入未充分探索的ASC区室,该方法能够高效地发现抗体,并对保护性抗体的产生进行免疫学研究。

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