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一种半自动高通量瞬时转染系统的开发。

Development of a semi-automated high throughput transient transfection system.

作者信息

Bos Aaron B, Duque Joseph N, Bhakta Sunil, Farahi Farzam, Chirdon Lindsay A, Junutula Jagath R, Harms Peter D, Wong Athena W

机构信息

Department of Early Stage Cell Culture, Genentech Inc., 1 DNA Way, South San Francisco, CA 94080, USA.

Department of Molecular Oncology, Genentech Inc., 1 DNA Way, South San Francisco, CA 94080, USA.

出版信息

J Biotechnol. 2014 Jun 20;180:10-6. doi: 10.1016/j.jbiotec.2014.03.027. Epub 2014 Apr 1.

DOI:10.1016/j.jbiotec.2014.03.027
PMID:24704608
Abstract

Transient transfection of mammalian cells provides a rapid method of producing protein for research purposes. Combining the transient transfection protein expression system with new automation technologies developed for the biotechnology industry would enable a high throughput protein production platform that could be utilized to generate a variety of different proteins in a short amount of time. These proteins could be used for an assortment of studies including proof of concept, antibody development, and biological structure and function. Here we describe such a platform: a semi-automated process for PEI-mediated transient protein production in tubespins at a throughput of 96 transfections at a time using a Biomek FX(P) liquid handling system. In one batch, 96 different proteins can be produced in milligram amounts by PEI transfection of HEK293 cells cultured in 50 mL tubespins. Methods were developed for the liquid handling system to automate the different processes associated with transient transfections such as initial cell seeding, DNA:PEI complex activation and DNA:PEI complex addition to the cells. Increasing DNA:PEI complex incubation time resulted in lower protein expression. To minimize protein production variability, the methods were further optimized to achieve consistent cell seeding, control the DNA:PEI incubation time and prevent cross-contamination among different tubespins. This semi-automated transfection process was applied to express 520 variants of a human IgG1 (hu IgG1) antibody.

摘要

哺乳动物细胞的瞬时转染为研究目的生产蛋白质提供了一种快速方法。将瞬时转染蛋白表达系统与为生物技术行业开发的新自动化技术相结合,将能够构建一个高通量蛋白质生产平台,该平台可用于在短时间内生成多种不同的蛋白质。这些蛋白质可用于各种研究,包括概念验证、抗体开发以及生物结构与功能研究。在此,我们描述这样一个平台:一种使用Biomek FX(P)液体处理系统在试管中进行PEI介导的瞬时蛋白质生产的半自动化过程,一次可进行96次转染。在一批实验中,通过对培养于50 mL试管中的HEK293细胞进行PEI转染,可生产毫克量的96种不同蛋白质。针对液体处理系统开发了方法,以自动化与瞬时转染相关的不同过程,如初始细胞接种、DNA:PEI复合物激活以及向细胞中添加DNA:PEI复合物。延长DNA:PEI复合物孵育时间会导致蛋白质表达降低。为了最小化蛋白质生产的变异性,对方法进行了进一步优化,以实现一致的细胞接种、控制DNA:PEI孵育时间并防止不同试管之间的交叉污染。这种半自动化转染过程被应用于表达人IgG1(hu IgG1)抗体的520个变体。

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