Ng Jessica P Z, Mariati Mariati, Bi Jiawu, Chang Matthew Wook, Yang Yuansheng
Bioprocessing Technology Institute (BTI), Agency for Science, Technology and Research (A*STAR), 20 Biopolis Way, #03-01 Centros, Singapore 138668, Singapore.
Institute of Molecular Cell Biology (IMCB), Agency for Science, Technology and Research (A*STAR), 61 Biopolis Dr, #07-01 Proteos, Singapore 138673, Singapore.
Antibodies (Basel). 2025 Apr 28;14(2):38. doi: 10.3390/antib14020038.
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.
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.
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.
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.
我们开发了一种基于靶向整合的CHO细胞平台,用于同时进行抗体展示和分泌,从而实现从抗体库筛选到生产的简化过渡,而无需重新克隆抗体基因。
该平台由具有单拷贝着陆平台的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平台中。通过在重链(HC)和膜锚之间掺入最小弗林蛋白酶切割序列(mFCS)、RRKR和各种2A肽来设计双功能载体。
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肽中的突变产生了一系列展示与分泌比率。然而,一部分分泌抗体保留了与HC多肽相连的2A残基。进一步分析表明,修饰2A肽的前五个氨基酸显著影响弗林蛋白酶切割效率,导致含有mFCS-2A变体组合的靶向载体具有不同的展示与分泌比率。为了克服这一问题,我们设计了九个氨基酸的FCS变体,当将其置于HC和膜锚之间时,可提供一系列展示与分泌比率,并消除了分泌抗体中2A残基附着的问题。展示水平较低的载体在区分表达具有紧密匹配结合亲和力的高亲和力抗体的细胞方面更有效。该平台在分离表达高亲和力抗体的细胞方面也表现出高灵敏度,并支持强大的抗体生产。
这种基于靶向整合的CHO平台能够高效、在形式上筛选和生产具有可调展示与分泌谱的抗体。它为加速功能性、可制造治疗性抗体的开发提供了一个强大且可扩展的工具。