时间轴
计算生物学
糖基化
克隆(Java方法)
基因组
药物开发
生物
效价
大流行
2019年冠状病毒病(COVID-19)
病毒学
生物技术
遗传学
药品
基因
疾病
病毒
医学
药理学
地理
病理
考古
传染病(医学专业)
作者
Chad A. Hall,Rachel H. Kravitz,Karl Johnson,Nicholas A. Sanek,Payel Maiti,Keith R. Ziemba,Jia Liu,Dmitri O. Andreev,Victoria L. Chrostowski,Ian J. Collins,Gregory T. Bleck
出处
期刊:Authorea - Authorea
日期:2022-12-15
被引量:1
标识
DOI:10.22541/au.167113298.81559773/v1
摘要
Reducing drug development timelines is an industry-wide goal to bring medicines to patients in need more quickly. This was exemplified in the COVID-19 pandemic where reducing development timelines had a direct impact on the number of lives lost to the disease. The use of drug substance produced using cell pools, as opposed to clones, has the potential to shorten development timelines. Toward this goal, we have developed a novel technology, GPEx® Lightning, that allows for rapid, reproducible, targeted recombination of transgenes into more than 200 Dock sites in the CHO genome. This allows for rapid production of high expressing stable cell pools and clones that reach titers of 4 to 12 g/L in generic fed-batch production. These pools and clones are highly stable in both titer and glycosylation, showing strong similarity in glycosylation profiles.
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