中国仓鼠卵巢细胞
转染
重组DNA
抗体
效价
细胞培养
单克隆抗体
体外
DNA
化学
细胞生物学
生物
分子生物学
计算生物学
基因
生物化学
免疫学
遗传学
作者
Elizabeth Greene,Daniela Cazacu,Ninkka Tamot,Steven Castellano,Akshita Datar,Anthony Kronkaitis,Douglas H. Gebhard,Jon Reed,Paul Mawson,Lore Florin,Nicholas A. Rossi,Anthony Lauer,Laura Juckem,Andrew E. Nixon,Till Wenger,Saurabh Sen
标识
DOI:10.1002/biot.202000251
摘要
Transient gene expression (TGE) using mammalian cells is an extensively used technology for the production of antibodies and recombinant proteins and has been widely adopted by both academic and industrial labs. Chinese Hamster Ovary (CHO) cells have become one of the major workhorses for TGE of recombinant antibodies due to their attractive features: post-translational modifications, adaptation to high cell densities, and use of serum-free media. In this study, we describe the optimization of parameters for TGE for antibodies from CHO cells. Through a matrix evaluation of multiple factors including inoculum, transfection conditions, amount and type of DNA used, and post-transfection culture conditions, we arrived at an uniquely optimized process with higher titer and reduced costs and time, thus increasing the overall efficiency of early antibody material supply. We further investigated the amount of coding DNA used in TGE and the influence of kinetics and size of the transfection complex on the in vitro efficiency of the transfection. We present here the first report of an optimized TGE platform using Filler DNA in an early drug discovery setting for the screening and production of therapeutic mAbs.
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