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通过使用培养基混合的严格组分重排来改进细胞培养基。

Cell culture medium improvement by rigorous shuffling of components using media blending.

机构信息

Biotech Process Sciences, Merck Serono Biotech Center, 1809, Fenil-sur-Corsier, Switzerland,

出版信息

Cytotechnology. 2013 Jan;65(1):31-40. doi: 10.1007/s10616-012-9462-1. Epub 2012 Jun 14.

Abstract

A novel high-throughput methodology for the simultaneous optimization of many cell culture media components is presented. The method is based on the media blending approach which has several advantages as it works with ready-to-use media. In particular it allows precise pH and osmolarity adjustments and eliminates the need of concentrated stock solutions, a frequent source of serious solubility issues. In addition, media blending easily generates a large number of new compositions providing a remarkable screening tool. However, media blending designs usually do not provide information on distinct factors or components that are causing the desired improvements. This paper addresses this last point by considering the concentration of individual medium components to fix the experimental design and for the interpretation of the results. The extended blending strategy was used to reshuffle the 20 amino acids in one round of experiments. A small set of 10 media was specifically designed to generate a large number of mixtures. 192 mixtures were then prepared by media blending and tested on a recombinant CHO cell line expressing a monoclonal antibody. A wide range of performances (titers and viable cell density) was achieved from the different mixtures with top titers significantly above our previous results seen with this cell line. In addition, information about major effects of key amino acids on cell densities and titers could be extracted from the experimental results. This demonstrates that the extended blending approach is a powerful experimental tool which allows systematic and simultaneous reshuffling of multiple medium components.

摘要

本文提出了一种新颖的高通量方法,用于同时优化许多细胞培养介质成分。该方法基于介质混合方法,具有几个优点,因为它可以使用即用型培养基。特别是,它允许精确调整 pH 值和渗透压,并消除了浓缩储备溶液的需求,浓缩储备溶液是严重溶解度问题的常见来源。此外,介质混合可以轻松生成大量新的成分,提供了一种出色的筛选工具。然而,介质混合设计通常不能提供导致所需改进的不同因素或成分的信息。本文通过考虑个别介质成分的浓度来解决最后一个问题,以固定实验设计并解释结果。扩展的混合策略用于在一轮实验中重新排列 20 种氨基酸。专门设计了一组 10 种培养基来生成大量混合物。然后通过介质混合制备了 192 种混合物,并在表达单克隆抗体的重组 CHO 细胞系上进行了测试。从不同的混合物中获得了广泛的性能(滴度和活细胞密度),最高滴度明显高于我们以前在该细胞系上看到的结果。此外,还可以从实验结果中提取关于关键氨基酸对细胞密度和滴度的主要影响的信息。这表明扩展的混合方法是一种强大的实验工具,允许系统地同时重新排列多个介质成分。

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