DiDonato Michael, Deacon Ashley M, Klock Heath E, McMullan Daniel, Lesley Scott A
The Joint Center for Structural Genomics, and The Genomics Institute of the Novartis Research Foundation, 10675 John Jay Hopkins Drive, San Diego, CA 92121, USA.
J Struct Funct Genomics. 2004;5(1-2):133-46. doi: 10.1023/B:JSFG.0000029194.04443.50.
The wealth of genomic data available for many organisms has set the stage for the next phase of structure-function analysis. High-throughput structural genomics is currently the method of choice for rapid analysis of protein structure-function relationships on a proteome-wide basis. The Joint Center for Structural Genomics (JCSG), established in 2000 under the NIH/NIGMS Protein Structure Initiative, has developed and implemented an integrated high-throughput structure pipeline and applied it in a 2-tiered approach to mining the proteome of the thermophilic bacterium Thermotoga maritima. In the first tier, the successful application of this integrated pipeline has resulted in the cloning and expression of 73% of the T. maritima proteome (1376 out of 1877 predicted genes), and has identified 465 proteins which produced crystal hits. These 465 proteins were compared with existing structural information and a subset of 269 targets were selected to process towards structure determination in a second tier effort. To date, the JCSG pipeline applied to the Thermotoga maritima proteome has resulted in 55 new structures and has identified 6 novel folds and continues to identify structures with novel features.
许多生物体可获取的丰富基因组数据为下一阶段的结构-功能分析奠定了基础。高通量结构基因组学是目前在全蛋白质组范围内快速分析蛋白质结构-功能关系的首选方法。2000年根据美国国立卫生研究院/国立综合医学科学研究所蛋白质结构计划成立的结构基因组学联合中心(JCSG),已开发并实施了一个集成的高通量结构流程,并将其应用于一种两层方法来挖掘嗜热细菌海栖热袍菌的蛋白质组。在第一层,这种集成流程的成功应用已导致海栖热袍菌蛋白质组73%(1877个预测基因中的1376个)的克隆和表达,并鉴定出465种产生晶体衍射信号的蛋白质。将这465种蛋白质与现有的结构信息进行比较,并选择269个目标的一个子集进行第二层的结构测定工作。迄今为止,应用于海栖热袍菌蛋白质组的JCSG流程已产生55个新结构,鉴定出6种新折叠,并继续鉴定具有新特征的结构。