Mayer Michael R, Dailey Tamara A, Baucom Clay M, Supernak Jill L, Grady Michael C, Hawk Harris E, Dailey Harry A
Southeast Collaboratory for Structural Genomics, A222 Life Sciences, Athens, GA 30602-7229, USA.
J Struct Funct Genomics. 2004;5(1-2):159-65. doi: 10.1023/B:JSFG.0000029202.77832.34.
The human protein production group at the Southeast Collaboratory for Structural Genomics is charged with producing human proteins for both X-ray crystallography and NMR structural studies. Eukaryotic, and human proteins in particular, are notoriously difficult to express in bacterial systems. For various reasons, T7-based expression often results in protein expressed in an insoluble form. Overcoming this requires either introduction of a step to screen expression conditions or inclusion of a troublesome refolding step during purification. Our laboratory uses a trc-based expression vector that addresses many of the difficulties of the commonly used T7-based expression systems. Proteins expressed under the trc promoter, a weak promoter compared to the strong T7 promoter, are produced in a soluble form and include necessary cofactors. The details of this system will be discussed.
东南结构基因组学协作实验室的人类蛋白质生产团队负责生产用于X射线晶体学和核磁共振结构研究的人类蛋白质。真核生物蛋白质,尤其是人类蛋白质,在细菌系统中表达 notoriously difficult。由于各种原因,基于T7的表达通常会导致蛋白质以不溶性形式表达。要克服这一问题,要么引入一个步骤来筛选表达条件,要么在纯化过程中包含一个麻烦的重折叠步骤。我们实验室使用一种基于trc的表达载体,该载体解决了常用的基于T7的表达系统的许多难题。在trc启动子(与强T7启动子相比是弱启动子)控制下表达的蛋白质以可溶形式产生,并包含必要的辅因子。将讨论该系统的详细情况。