Rational design of a host cell protein heat precipitation step simplifies the subsequent purification of recombinant proteins from tobacco

被引:35
|
作者
Buyel, J. F. [1 ]
Gruchow, H. M. [2 ]
Boes, A. [2 ]
Fischer, R. [1 ,2 ]
机构
[1] Rhein Westfal TH Aachen, Inst Mol Biotechnol, Worringer Weg 1, D-52074 Aachen, Germany
[2] Fraunhofer Inst Mol Biol & Appl Ecol, D-52074 Aachen, Germany
基金
欧洲研究理事会;
关键词
Bioprocess design; Bioseparations; Downstream processing; Purification; Plant-derived biopharmaceuticals; Heat precipitation; PHARMACEUTICAL PROTEINS; POLYPEPTIDE FUSIONS; QUALITY ATTRIBUTES; PREDICTIVE MODELS; TRANSGENIC PLANTS; COLD DENATURATION; AFFINITY TAGS; EXPRESSION; ANTIBODY; STABILITY;
D O I
10.1016/j.bej.2014.04.015
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The benefits of plants for the production of biopharmaceutical proteins include the ease of scale-up and the low pathogen burden, but the purification of target proteins is often affected by low expression levels and the abundance of host cell proteins in leaf extracts. These factors can significantly diminish the competitiveness of plant-based expression systems. We therefore compared three different heat precipitation steps that remove most host cell proteins while leaving a heat-stable candidate malaria vaccine protein in solution. A design-of-experiments approach was used to test each method and analyze the resulting data, allowing us to model and optimize the corresponding process. The heat treatment of leaves was superior to both methods for the heat treatment of extracts in terms of process-scale implementation, energy consumption and speed. We discuss additional benefits and drawbacks of these methods compared to current strategies for the purification of biopharmaceutical proteins produced in plants. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:162 / 170
页数:9
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