School of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney NSW 2052, Australia.
School of Biological Sciences and Department of Chemical Engineering, Monash University, VIC 3800, Australia.
Biotechnol Adv. 2009 Nov-Dec;27(6):1036-1042. doi: 10.1016/j.biotechadv.2009.05.009. Epub 2009 May 20.
Plants and plant tissue cultures are used as host systems for expression of foreign proteins including antibodies, vaccines and other therapeutic agents. Recombinant or stably transformed plants and plant cell cultures have been applied for foreign protein production for about 20 years. Because the product concentration achieved exerts a major influence on process economics, considerable efforts have been made by commercial and academic research groups to improve foreign protein expression levels. However, post-synthesis product losses due to protease activity within plant tissues and/or extracellular protein adsorption in plant cell cultures can negate the benefits of molecular or genetic enhancement of protein expression. Transient expression of foreign proteins using plant viral vectors is also a practical approach for producing foreign proteins in plants. Adaptation of this technology is required to allow infection and propagation of engineered viruses in plant tissue cultures for transient protein expression in vitro.
植物和植物组织培养被用作表达外源蛋白的宿主系统,包括抗体、疫苗和其他治疗剂。重组或稳定转化的植物和植物细胞培养已经用于外源蛋白生产约 20 年。由于产品浓度对外界蛋白生产的经济性有重大影响,因此商业和学术研究小组都做出了相当大的努力来提高外源蛋白的表达水平。然而,由于植物组织内的蛋白酶活性和/或植物细胞培养中外源蛋白的吸附导致的翻译后产物损失,可能会抵消分子或遗传增强蛋白表达的好处。利用植物病毒载体瞬时表达外源蛋白也是在植物中生产外源蛋白的一种实用方法。需要对这项技术进行改造,以允许工程病毒在植物组织培养中感染和增殖,从而实现体外瞬时蛋白表达。