Schmidt Peter M, Abdo Michael, Butcher Rebecca E, Yap Min-Yin, Scotney Pierre D, Ramunno Melanie L, Martin-Roussety Genevieve, Owczarek Catherine, Hardy Matthew P, Chen Chao-Guang, Fabri Louis J
CSL Limited, BIO21 Institute, 30 Flemington Road, Parkville, Victoria 3010, Australia.
Perkin Elmer, 530-540 Springvale Road, Glen Waverley, Victoria 3150, Australia.
J Chromatogr A. 2016 Jul 15;1455:9-19. doi: 10.1016/j.chroma.2016.05.076. Epub 2016 May 24.
Monoclonal antibodies (mAbs) have become the fastest growing segment in the drug market with annual sales of more than 40 billion US$ in 2013. The selection of lead candidate molecules involves the generation of large repertoires of antibodies from which to choose a final therapeutic candidate. Improvements in the ability to rapidly produce and purify many antibodies in sufficient quantities reduces the lead time for selection which ultimately impacts on the speed with which an antibody may transition through the research stage and into product development. Miniaturization and automation of chromatography using micro columns (RoboColumns(®) from Atoll GmbH) coupled to an automated liquid handling instrument (ALH; Freedom EVO(®) from Tecan) has been a successful approach to establish high throughput process development platforms. Recent advances in transient gene expression (TGE) using the high-titre Expi293F™ system have enabled recombinant mAb titres of greater than 500mg/L. These relatively high protein titres reduce the volume required to generate several milligrams of individual antibodies for initial biochemical and biological downstream assays, making TGE in the Expi293F™ system ideally suited to high throughput chromatography on an ALH. The present publication describes a novel platform for purifying Expi293F™-expressed recombinant mAbs directly from cell-free culture supernatant on a Perkin Elmer JANUS-VariSpan ALH equipped with a plate shuttle device. The purification platform allows automated 2-step purification (Protein A-desalting/size exclusion chromatography) of several hundred mAbs per week. The new robotic method can purify mAbs with high recovery (>90%) at sub-milligram level with yields of up to 2mg from 4mL of cell-free culture supernatant.
单克隆抗体(mAb)已成为药物市场中增长最快的领域,2013年的年销售额超过400亿美元。先导候选分子的选择涉及生成大量抗体库,以便从中选择最终的治疗候选物。快速大量生产和纯化多种抗体能力的提高缩短了选择的前置时间,这最终影响了抗体从研究阶段过渡到产品开发的速度。使用微柱(Atoll GmbH公司的RoboColumns(®))与自动液体处理仪器(ALH;Tecan公司的Freedom EVO(®))相结合实现色谱分析的小型化和自动化,是建立高通量工艺开发平台的成功方法。使用高滴度Expi293F™系统进行瞬时基因表达(TGE)的最新进展,已使重组单克隆抗体滴度超过500mg/L。这些相对较高的蛋白质滴度减少了为初始生化和生物下游分析生成几毫克单个抗体所需的体积,使得Expi293F™系统中的TGE非常适合在ALH上进行高通量色谱分析。本出版物描述了一种新型平台,用于在配备板穿梭装置的Perkin Elmer JANUS-VariSpan ALH上直接从无细胞培养上清液中纯化Expi293F™表达的重组单克隆抗体。该纯化平台允许每周自动对数百种单克隆抗体进行两步纯化(蛋白A-脱盐/尺寸排阻色谱法)。这种新的机器人方法可以在亚毫克水平以高达90%以上的回收率纯化单克隆抗体,从4mL无细胞培养上清液中可获得高达2mg的产量。