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利用piggyBac转座子系统在稳定的中国仓鼠卵巢(CHO)细胞库中的多基因表达

Multigene expression in stable CHO cell pools generated with the piggyBac transposon system.

作者信息

Balasubramanian Sowmya, Wurm Florian M, Hacker David L

机构信息

Laboratory of Cellular Biotechnology (LBTC), École Polytechnique Fédérale de Lausanne (EPFL), Lausanne, CH-1015, Switzerland.

Protein Expression Core Facility (PECF), École Polytechnique Fédérale de Lausanne (EPFL), Lausanne, CH-1015, Switzerland.

出版信息

Biotechnol Prog. 2016 Sep;32(5):1308-1317. doi: 10.1002/btpr.2319. Epub 2016 Jul 13.

Abstract

Heterogenous populations of recombinant cells (cell pools) stably expressing 1-4 transgenes were generated from Chinese hamster overy (CHO) cells with the piggyBac (PB) transposon system. The cell pools produced different combinations of three model proteins-enhanced green fluorescent protein (EGFP), secreted alkaline phosphatase (SEAP), and a monoclonal IgG1 antibody. Each transgene was present on a separate PB donor plasmid with either the same or a different selection gene. In both cases, we obtained PB-derived cell pools with higher recombinant protein yields than from cell pools generated by conventional gene delivery. In PB-derived cell pools generated using a single selection agent, both protein production and the number of integrated copies of each transgene declined as the number of transfected transgenes increased. However, the total number of integrated transgenes was similar regardless of the number of different transgenes transfected. For PB-derived cell pools generated by selection of each transgene with a different selection agent, the total number of integrated transgenes increased with the number of transfected transgenes. The results suggest that the generation of cell pools producing multiple recombinant proteins is feasible and that the method is more efficient when each individual transgene is selected with a different marker. © 2016 American Institute of Chemical Engineers Biotechnol. Prog., 32:1308-1317, 2016.

摘要

利用猪尾巴(PB)转座子系统,从中国仓鼠卵巢(CHO)细胞中产生了稳定表达1 - 4个转基因的重组细胞异质群体(细胞池)。这些细胞池产生了三种模型蛋白——增强型绿色荧光蛋白(EGFP)、分泌性碱性磷酸酶(SEAP)和一种单克隆IgG1抗体的不同组合。每个转基因存在于带有相同或不同选择基因的单独PB供体质粒上。在这两种情况下,我们获得的源自PB的细胞池的重组蛋白产量均高于通过传统基因递送产生的细胞池。在使用单一选择剂产生的源自PB的细胞池中,随着转染转基因数量的增加,蛋白质产量和每个转基因的整合拷贝数均下降。然而,无论转染的不同转基因数量如何,整合转基因的总数相似。对于通过用不同选择剂选择每个转基因而产生的源自PB的细胞池,整合转基因的总数随着转染转基因数量的增加而增加。结果表明,产生多种重组蛋白的细胞池的产生是可行的,并且当用不同标记选择每个单独的转基因时,该方法更有效。© 2016美国化学工程师学会生物技术进展,32:1308 - 1317,2室。

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