A Targeted Integration-Based CHO Cell Platform for Simultaneous Antibody Display and Secretion.

IF 3 Q3 IMMUNOLOGY
Antibodies Pub Date : 2025-04-28 DOI:10.3390/antib14020038
Jessica P Z Ng, Mariati Mariati, Jiawu Bi, Matthew Wook Chang, Yuansheng Yang
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引用次数: 0

Abstract

Objective: We developed a targeted integration-based CHO cell platform for simultaneous antibody display and secretion, enabling a streamlined transition from antibody library screening to production without requiring the re-cloning of antibody genes.

Methods: The platform consists of a CHO master cell line with a single-copy landing pad, a helper vector expressing FLPe recombinase, and bi-functional targeting vectors. Recombinase-mediated cassette exchange was utilized to integrate targeting vectors into the landing pad. Bi-functional vectors were designed by incorporating a minimal furin cleavage sequence (mFCS), RRKR, and various 2A peptides between the heavy chain (HC) and a membrane anchor.

Results: Incomplete cleavage at the mFCS and 2A sites facilitated the expression of both membrane-bound and secreted antibodies, while mutations in the 2A peptide produced a range of display-to-secretion ratios. However, a fraction of secreted antibodies retained 2A residues attached to the HC polypeptides. Further analysis demonstrated that modifying the first five amino acids of the 2A peptide significantly influenced furin cleavage efficiency, resulting in different display-to-secretion ratios for targeting vectors containing mFCS-2A variant combinations. To overcome this, we designed nine-amino-acid FCS variants that, when placed between the HC and membrane anchor, provided a range of display-to-secretion ratios and eliminated the issue of attached 2A residues in the secreted antibodies. Vectors with lower display levels proved more effective at distinguishing cells expressing high-affinity antibodies with closely matched binding affinities. The platform also demonstrated high sensitivity in isolating high-affinity antibody-expressing cells and supported robust antibody production.

Conclusion: This targeted integration-based CHO platform enables efficient, in-format screening and production of antibodies with tunable display-to-secretion profiles. It provides a powerful and scalable tool for accelerating the development of functional, manufacturable therapeutic antibodies.

基于靶向整合的CHO细胞平台用于同时显示和分泌抗体。
目的:我们开发了一种基于靶向整合的CHO细胞平台,用于同时显示和分泌抗体,使从抗体文库筛选到生产的简化过渡无需重新克隆抗体基因。方法:该平台由CHO主细胞系、表达FLPe重组酶的辅助载体和双功能靶向载体组成。利用重组酶介导的盒式交换将靶向载体整合到着陆台上。通过在重链(HC)和膜锚点之间加入最小furin裂解序列(mFCS)、RRKR和各种2A肽,设计了双功能载体。结果:mFCS和2A位点的不完全切割促进了膜结合抗体和分泌抗体的表达,而2A肽的突变产生了一系列的显示-分泌比。然而,一部分分泌的抗体保留了附着在HC多肽上的2A残基。进一步分析表明,修饰2A肽的前5个氨基酸显著影响furin的切割效率,导致含有mFCS-2A变异组合的靶向载体的显示-分泌比不同。为了克服这个问题,我们设计了9个氨基酸的FCS变体,当放置在HC和膜锚点之间时,提供了一系列的显示-分泌比,并消除了分泌抗体中附着2A残基的问题。低显示水平的载体被证明在区分表达高亲和力抗体的细胞时更有效,这些抗体具有紧密匹配的结合亲和力。该平台在分离高亲和力抗体表达细胞方面也表现出高灵敏度,并支持稳健的抗体生产。结论:这种基于靶向整合的CHO平台能够高效、按格式筛选和生产具有可调显示-分泌谱的抗体。它为加速开发功能性的、可制造的治疗性抗体提供了一个强大的、可扩展的工具。
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来源期刊
Antibodies
Antibodies IMMUNOLOGY-
CiteScore
7.10
自引率
6.40%
发文量
68
审稿时长
11 weeks
期刊介绍: Antibodies (ISSN 2073-4468), an international, peer-reviewed open access journal which provides an advanced forum for studies related to antibodies and antigens. It publishes reviews, research articles, communications and short notes. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. Full experimental and/or methodical details must be provided. Electronic files or software regarding the full details of the calculation and experimental procedure - if unable to be published in a normal way - can be deposited as supplementary material. This journal covers all topics related to antibodies and antigens, topics of interest include (but are not limited to): antibody-producing cells (including B cells), antibody structure and function, antibody-antigen interactions, Fc receptors, antibody manufacturing antibody engineering, antibody therapy, immunoassays, antibody diagnosis, tissue antigens, exogenous antigens, endogenous antigens, autoantigens, monoclonal antibodies, natural antibodies, humoral immune responses, immunoregulatory molecules.
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