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高通量生产用于结晶的人蛋白:SGC 的经验。

High-throughput production of human proteins for crystallization: the SGC experience.

机构信息

Structural Genomics Consortium, University of Oxford, Old Road Campus Research Building, Oxford, UK.

出版信息

J Struct Biol. 2010 Oct;172(1):3-13. doi: 10.1016/j.jsb.2010.06.008. Epub 2010 Jun 10.

Abstract

Producing purified human proteins with high yield and purity remains a considerable challenge. We describe the methods utilized in the Structural Genomics Consortium (SGC) in Oxford, resulting in successful purification of 48% of human proteins attempted; of those, the structures of approximately 40% were solved by X-ray crystallography. The main driver has been the parallel processing of multiple (typically 9-20) truncated constructs of each target; modest diversity in vectors and host systems; and standardized purification procedures. We provide method details as well as data on the properties of the constructs leading to crystallized proteins and the impact of methodological variants. These can be used to formulate guidelines for initial approaches to expression of new eukaryotic proteins.

摘要

用高产率和高纯度生产纯化的人类蛋白质仍然是一个相当大的挑战。我们描述了牛津结构基因组学联盟(SGC)中使用的方法,这些方法成功地纯化了尝试的 48%的人类蛋白质;其中,约 40%的蛋白质通过 X 射线晶体学解决了其结构。主要驱动力是对每个目标的多个(通常为 9-20 个)截断构建体的并行处理;载体和宿主系统的适度多样性;以及标准化的纯化程序。我们提供方法细节以及关于导致结晶蛋白的构建体的特性以及方法变体的影响的数据。这些可以用于制定新的真核蛋白质表达初始方法的指南。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9903/2938586/d90853590d89/fx1.jpg

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