Sievert Volker, Ergin Asgar, Büssow Konrad
Max Planck Institute for Molecular Genetics, Department of Vertebrate Genomics, Protein Structure Factory, Berlin, Germany.
Methods Mol Biol. 2008;426:163-73. doi: 10.1007/978-1-60327-058-8_9.
The systematic structural analysis of many target proteins involves generating expression clones in high throughput. This requires robust laboratory procedures and benefits from laboratory automation and data management systems. This chapter gives an overview of the Protein Structure Factory, a structural genomics project focusing on human proteins, and presents the authors' method for cloning bacterial expression clones with the restriction enzymes BamHI and NotI and compatible enzymes. PCR amplification, product purification and digestion and vector ligation were adapted to the 96-well microtiter plate format.
对许多靶蛋白进行系统的结构分析需要高通量地生成表达克隆。这需要可靠的实验室程序,并且受益于实验室自动化和数据管理系统。本章概述了蛋白质结构工厂,这是一个专注于人类蛋白质的结构基因组学项目,并介绍了作者使用限制性内切酶BamHI和NotI以及兼容酶克隆细菌表达克隆的方法。PCR扩增、产物纯化、消化和载体连接都适用于96孔微量滴定板形式。