Institute of Molecular Biotechnology, Graz University of Technology, Petersgasse 14, 8010 Graz, Austria.
Microb Cell Fact. 2009 Dec 29;8:69. doi: 10.1186/1475-2859-8-69.
The last four years have brought exciting progress in membrane protein research. Finally those many efforts that have been put into expression of eukaryotic membrane proteins are coming to fruition and enable to solve an ever-growing number of high resolution structures. In the past, many skilful optimization steps were required to achieve sufficient expression of functional membrane proteins. Optimization was performed individually for every membrane protein, but provided insight about commonly encountered bottlenecks and, more importantly, general guidelines how to alleviate cellular limitations during microbial membrane protein expression. Lately, system-wide analyses are emerging as powerful means to decipher cellular bottlenecks during heterologous protein production and their use in microbial membrane protein expression has grown in popularity during the past months.This review covers the most prominent solutions and pitfalls in expression of eukaryotic membrane proteins using microbial hosts (prokaryotes, yeasts), highlights skilful applications of our basic understanding to improve membrane protein production. Omics technologies provide new concepts to engineer microbial hosts for membrane protein production.
过去四年中,膜蛋白研究取得了令人兴奋的进展。终于,多年来在真核膜蛋白表达方面的努力开始取得成果,能够解决越来越多的高分辨率结构问题。过去,需要许多巧妙的优化步骤才能实现功能性膜蛋白的充分表达。针对每种膜蛋白都进行了单独的优化,但提供了有关常见瓶颈的深入了解,更重要的是,提供了在微生物膜蛋白表达过程中减轻细胞限制的一般指导原则。最近,系统级分析作为一种强大的手段,用于破译异源蛋白生产过程中的细胞瓶颈,并且在过去几个月中,它们在微生物膜蛋白表达中的应用越来越受欢迎。本综述涵盖了使用微生物宿主(原核生物、酵母)表达真核膜蛋白的最突出的解决方案和陷阱,强调了我们对基本理解的巧妙应用,以提高膜蛋白的生产。组学技术为用于膜蛋白生产的微生物宿主的工程提供了新的概念。