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利用 Leap-In 转座子系统生成高表达的中国仓鼠卵巢细胞池。

Generation of High Expressing Chinese Hamster Ovary Cell Pools Using the Leap-In Transposon System.

机构信息

Bioprocess Research and Development, Eli Lilly and Company, LTC-North, 1200 Kentucky AvenueIndianapolis, IN, 46221, USA.

Biotechnology Discovery Research, Lilly Research Laboratories, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN, 46225, USA.

出版信息

Biotechnol J. 2018 Oct;13(10):e1700748. doi: 10.1002/biot.201700748. Epub 2018 Jun 11.

Abstract

Clonally derived cell lines (CDCL) from Chinese Hamster Ovary (CHO) host cell lines, remain the most popular method to manufacture therapeutic proteins. However, CHO cell pools are increasingly being used as an alternate method to produce therapeutic proteins for preclinical drug development in an effort to shorten the time required for new drug development. It is essential that these CHO pools exhibit the desired attributes of CHO CDCLs such as high protein titers and consistent product quality attributes (PQAs). In this study the authors evaluated the Leap-In Transposase®, for the expression of four different proteins (three mAbs and one Bispecific mAb). The resultant pool titers ranges from 2.0 to 5.0 g L for the four proteins compared to 1.5-3.3 g L from the respective control pools (generated by random gene integration). The resultant cell pools are a homogeneously expressing cell population. The average gene copy numbers are similar or lower in the evaluation pools relative to the control pools. The higher titers in the evaluation pools are attributed to higher levels of both IgG-LC and IgG-HC mRNA. In conclusion, the Leap-In transposase generates high titer, homogeneous CHO pools in a short time-period without introducing any undesired PQAs.

摘要

来自中国仓鼠卵巢(CHO)宿主细胞系的克隆衍生细胞系(CDCL)仍然是制造治疗性蛋白的最流行方法。然而,CHO 细胞池越来越多地被用作替代方法来生产治疗性蛋白,用于临床前药物开发,以缩短新药开发所需的时间。至关重要的是,这些 CHO 池表现出与 CHO CDCL 相同的特性,如高蛋白滴度和一致的产品质量属性(PQAs)。在这项研究中,作者评估了 Leap-In Transposase®,用于表达四种不同的蛋白质(三种 mAb 和一种双特异性 mAb)。与各自的对照池(通过随机基因整合产生)相比,四种蛋白质的所得池滴度范围为 2.0 至 5.0 g/L,而对照池为 1.5-3.3 g/L。所得的细胞池是均一表达的细胞群体。与对照池相比,评估池中的平均基因拷贝数相似或更低。评估池中的高滴度归因于 IgG-LC 和 IgG-HC mRNA 的水平更高。总之,Leap-In 转座酶在短时间内产生高滴度、均一的 CHO 池,而不会引入任何不良的 PQAs。

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