从单个小鼠B细胞中快速产生抗原特异性单克隆抗体。

Xuanxiu Ren, Yiwei Zhang, Gan Zhang, Shangyu Yang, Feiyang Yu, Rao Cheng, Zengqin Deng, Haiyan Zhao
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引用次数: 0

摘要

从抗原特异性B细胞中鉴定免疫球蛋白(Ig)基因对于理解免疫反应和产生用于诊断和治疗目的的单克隆抗体至关重要。尽管基于单B细胞pcr的小鼠抗体开发已经建立,但仍存在一些实际挑战。在这里,我们提出了一种优化的方案,用于从单个抗原特异性小鼠B细胞中测序和克隆抗体可变区域,以及高通量抗体表达和表征。该方法建立在现有技术的基础上,结合实验室改进和详细的故障排除见解。通过整合荧光活化细胞分选(FACS)与逆转录聚合酶链反应(RT-PCR)来扩增免疫球蛋白重链和轻链基因,以及抗体表达的12孔格式,我们的改进方法能够高效地生产单克隆抗体和功能筛选,从而加快抗体发现工作流程,跨越一系列实验应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Rapid generation of antigen-specific monoclonal antibodies from single mouse B cells.

Rapid generation of antigen-specific monoclonal antibodies from single mouse B cells.

Rapid generation of antigen-specific monoclonal antibodies from single mouse B cells.

Identifying immunoglobulin (Ig) genes from antigen-specific B cells is crucial for understanding immune responses and generating monoclonal antibodies for diagnostic and therapeutic purposes. Despite single B cell PCR-based mouse antibody development is well established, several practical challenges remain. Here, we present an optimized protocol for the sequencing and cloning of variable regions of antibodies from single antigen-specific mouse B cells, along with high-throughput antibody expression and characterization. This method builds upon existing techniques, incorporating laboratory refinements and detailed troubleshooting insights. By integrating fluorescence-activated cell sorting (FACS) with reverse transcription polymerase chain reaction (RT-PCR) to amplify immunoglobulin heavy and light chain genes, along with a 12-well format for antibody expression, our refined approach enables efficient monoclonal antibody production and functional screening, thereby accelerating the antibody discovery workflow across a range of experimental applications.

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