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微生物制药厂。

Microbial factories for recombinant pharmaceuticals.

机构信息

Institut de Biotecnologia i de Biomedicina, Universitat Autònoma de Barcelona, 08193 Barcelona, Spain.

出版信息

Microb Cell Fact. 2009 Mar 24;8:17. doi: 10.1186/1475-2859-8-17.

Abstract

Most of the hosts used to produce the 151 recombinant pharmaceuticals so far approved for human use by the Food and Drug Administration (FDA) and/or by the European Medicines Agency (EMEA) are microbial cells, either bacteria or yeast. This fact indicates that despite the diverse bottlenecks and obstacles that microbial systems pose to the efficient production of functional mammalian proteins, namely lack or unconventional post-translational modifications, proteolytic instability, poor solubility and activation of cell stress responses, among others, they represent convenient and powerful tools for recombinant protein production. The entering into the market of a progressively increasing number of protein drugs produced in non-microbial systems has not impaired the development of products obtained in microbial cells, proving the robustness of the microbial set of cellular systems (so far Escherichia coli and Saccharomyces cerevisae) developed for protein drug production. We summarize here the nature, properties and applications of all those pharmaceuticals and the relevant features of the current and potential producing hosts, in a comparative way.

摘要

迄今为止,大多数被美国食品和药物管理局 (FDA) 和/或欧洲药品管理局 (EMEA) 批准用于人体的 151 种重组药物都是微生物细胞,无论是细菌还是酵母。这一事实表明,尽管微生物系统在有效生产功能性哺乳动物蛋白方面存在多种瓶颈和障碍,例如缺乏或非常规的翻译后修饰、蛋白不稳定、溶解性差和细胞应激反应激活等,但它们仍然是重组蛋白生产的便捷而强大的工具。越来越多的非微生物系统生产的蛋白药物进入市场,并没有影响到微生物细胞中获得的产品的发展,证明了用于蛋白药物生产的微生物细胞系统(迄今为止是大肠杆菌和酿酒酵母)的稳健性。在这里,我们以比较的方式总结了所有这些药物的性质、特性和应用,以及当前和潜在生产宿主的相关特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6095/2669800/10c07a715f0f/1475-2859-8-17-1.jpg

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