Raymond Amy, Haffner Taryn, Ng Nathan, Lorimer Don, Staker Bart, Stewart Lance
Seattle Structural Genomics Center for Infectious Disease (SSGCID), USA.
Acta Crystallogr Sect F Struct Biol Cryst Commun. 2011 Sep 1;67(Pt 9):992-7. doi: 10.1107/S1744309111026698. Epub 2011 Aug 13.
Any structural genomics endeavor, particularly ambitious ones such as the NIAID-funded Seattle Structural Genomics Center for Infectious Disease (SSGCID) and Center for Structural Genomics of Infectious Disease (CSGID), face technical challenges at all points of the production pipeline. One salvage strategy employed by SSGCID is combined gene engineering and structure-guided construct design to overcome challenges at the levels of protein expression and protein crystallization. Multiple constructs of each target are cloned in parallel using Polymerase Incomplete Primer Extension cloning and small-scale expressions of these are rapidly analyzed by capillary electrophoresis. Using the methods reported here, which have proven particularly useful for high-value targets, otherwise intractable targets can be resolved.
任何结构基因组学项目,尤其是像美国国立过敏与传染病研究所资助的西雅图传染病结构基因组学中心(SSGCID)和传染病结构基因组学中心(CSGID)这样雄心勃勃的项目,在生产流程的各个环节都面临技术挑战。SSGCID采用的一种补救策略是将基因工程与结构导向的构建体设计相结合,以克服蛋白质表达和蛋白质结晶层面的挑战。使用聚合酶不完全引物延伸克隆技术并行克隆每个靶标的多个构建体,并通过毛细管电泳快速分析这些构建体的小规模表达情况。使用本文报道的方法,已证明对高价值靶标特别有用,否则难以处理的靶标也可以得到解决。