Elsliger Marc André, Deacon Ashley M, Godzik Adam, Lesley Scott A, Wooley John, Wüthrich Kurt, Wilson Ian A
Department of Molecular Biology, The Scripps Research Institute, La Jolla, CA, USA.
Acta Crystallogr Sect F Struct Biol Cryst Commun. 2010 Oct 1;66(Pt 10):1137-42. doi: 10.1107/S1744309110038212. Epub 2010 Sep 30.
The Joint Center for Structural Genomics high-throughput structural biology pipeline has delivered more than 1000 structures to the community over the past ten years. The JCSG has made a significant contribution to the overall goal of the NIH Protein Structure Initiative (PSI) of expanding structural coverage of the protein universe, as well as making substantial inroads into structural coverage of an entire organism. Targets are processed through an extensive combination of bioinformatics and biophysical analyses to efficiently characterize and optimize each target prior to selection for structure determination. The pipeline uses parallel processing methods at almost every step in the process and can adapt to a wide range of protein targets from bacterial to human. The construction, expansion and optimization of the JCSG gene-to-structure pipeline over the years have resulted in many technological and methodological advances and developments. The vast number of targets and the enormous amounts of associated data processed through the multiple stages of the experimental pipeline required the development of variety of valuable resources that, wherever feasible, have been converted to free-access web-based tools and applications.
在过去十年中,结构基因组学联合中心的高通量结构生物学流程已向科学界交付了1000多个结构。JCSG为美国国立卫生研究院蛋白质结构计划(PSI)扩大蛋白质宇宙结构覆盖范围的总体目标做出了重大贡献,并在整个生物体的结构覆盖方面取得了重大进展。在选择进行结构测定之前,通过生物信息学和生物物理分析的广泛结合来处理目标,以有效地表征和优化每个目标。该流程在几乎每个步骤都使用并行处理方法,并且可以适应从细菌到人类的广泛蛋白质目标。多年来,JCSG基因到结构流程的构建、扩展和优化带来了许多技术和方法上的进步与发展。通过实验流程的多个阶段处理的大量目标和大量相关数据需要开发各种有价值的资源,在可行的情况下,这些资源已转换为基于网络的免费访问工具和应用程序。