化学
DNA
质粒
离心
分子生物学
基因表达
细胞生物学
HEK 293细胞
抗体
滤波器(信号处理)
细胞培养
基因
转录组
基因传递
过滤(数学)
外源DNA
工作流程
瞬态(计算机编程)
生物物理学
色谱法
计算生物学
协议(科学)
吞吐量
生物
作者
Gustaf Hederoth,Andrés de la Rosa,Ana Godec,Ximena Aguilar,Antonino Napoleone,Alex Petrovic,Nicole G. Metzendorf,Greta Hultqvist
标识
DOI:10.3389/fbioe.2025.1661193
摘要
Transient gene expression (TGE) is commonly used for the rapid production of protein-based therapeutics, including antibodies that require post-translational modifications. We previously published a protocol for efficient and cost-effective TGE of multispecific and multivalent antibodies. Here, we describe an optimized version of this protocol with key improvements in cost, workflow speed, and production capacity. First, the expensive Expi293 expression medium was replaced with BalanCD HEK293 medium, resulting in a substantial decrease in medium-related costs by approximately 90%. The addition of Pluronic F-68 was omitted, as the new medium already contains a similar surfactant. To minimize plasmid DNA usage, salmon sperm DNA was included as filler DNA during transfection, enabling a significant reduction in plasmid DNA input without compromising antibody yield. Second, the harvesting procedure was shortened from 2.5 h to just 15 min by adding the mineral compound diatomaceous earth (Celpure®) to the culture supernatant. This effectively absorbs and sequesters cells and debris, allowing rapid filtration without filter clogging or the previously required 1-h centrifugation step. Finally, we recommend high-flow rate HiScreen Fibro PrismA columns to further accelerate downstream antibody purification. Together, these improvements streamline the TGE workflow in Expi293F cells, enhance scalability, and increase throughput while maintaining efficiency in antibody production.
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