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利用优化的植物表达系统高效生产单克隆抗体

High Level Production of Monoclonal Antibodies Using an Optimized Plant Expression System.

作者信息

Diamos Andrew G, Hunter Joseph G L, Pardhe Mary D, Rosenthal Sun H, Sun Haiyan, Foster Bonnie C, DiPalma Michelle P, Chen Qiang, Mason Hugh S

机构信息

Center for Immunotherapy, Vaccines and Virotherapy, The Biodesign Institute, Arizona State University, Tempe, AZ, United States.

School of Life Sciences, Arizona State University, Tempe, AZ, United States.

出版信息

Front Bioeng Biotechnol. 2020 Jan 17;7:472. doi: 10.3389/fbioe.2019.00472. eCollection 2019.

Abstract

Biopharmaceuticals are a large and fast-growing sector of the total pharmaceutical market with antibody-based therapeutics accounting for over 100 billion USD in sales yearly. Mammalian cells are traditionally used for monoclonal antibody production, however plant-based expression systems have significant advantages. In this work, we showcase recent advances made in plant transient expression systems using optimized geminiviral vectors that can efficiently produce heteromultimeric proteins. Two, three, or four fluorescent proteins were coexpressed simultaneously, reaching high yields of 3-5 g/kg leaf fresh weight or ~50% total soluble protein. As a proof-of-concept for this system, various antibodies were produced using the optimized vectors with special focus given to the creation and production of a chimeric broadly neutralizing anti-flavivirus antibody. The variable regions of this murine antibody, 2A10G6, were codon optimized and fused to a human IgG1. Analysis of the chimeric antibody showed that it was efficiently expressed in plants at 1.5 g of antibody/kilogram of leaf tissue, can be purified to near homogeneity by a simple one-step purification process, retains its ability to recognize the Zika virus envelope protein, and potently neutralizes Zika virus. Two other monoclonal antibodies were produced at similar levels (1.2-1.4 g/kg). This technology will be a versatile tool for the production of a wide spectrum of pharmaceutical multi-protein complexes in a fast, powerful, and cost-effective way.

摘要

生物制药是整个制药市场中一个规模庞大且快速增长的领域,基于抗体的治疗药物年销售额超过1000亿美元。传统上,哺乳动物细胞用于生产单克隆抗体,然而基于植物的表达系统具有显著优势。在这项工作中,我们展示了利用优化的双生病毒载体在植物瞬时表达系统中取得的最新进展,该载体能够高效生产异源多聚体蛋白。同时共表达了两种、三种或四种荧光蛋白,产量高达3 - 5克/千克叶片鲜重或约占总可溶性蛋白的50%。作为该系统的概念验证,使用优化后的载体生产了各种抗体,特别关注了嵌合广谱中和抗黄病毒抗体的构建和生产。对这种鼠源抗体2A10G6的可变区进行密码子优化,并与人类IgG1融合。对嵌合抗体的分析表明,它在植物中能够高效表达,产量为1.5克抗体/千克叶片组织,可通过简单的一步纯化过程纯化至近乎同质,保留了识别寨卡病毒包膜蛋白的能力,并能有效中和寨卡病毒。另外两种单克隆抗体的产量也类似(1.2 - 1.4克/千克)。这项技术将成为一种通用工具,能够以快速、高效且经济高效的方式生产多种药物多蛋白复合物。

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