Busso Didier, Poussin-Courmontagne Pierre, Rosé David, Ripp Raymond, Litt Alain, Thierry Jean-Claude, Moras Dino
Département de Biologie et de Génomique Structurales, IGBMC, CNRS/INSERM/Université Louis Pasteur, Parc d'Innovation, 1 rue Laurent Fries, BP10142, 67404, Illkirch, cedex, France.
J Struct Funct Genomics. 2005;6(2-3):81-8. doi: 10.1007/s10969-005-1909-6.
Structural genomics programs are distributed worldwide and funded by large institutions such as the NIH in United-States, the RIKEN in Japan or the European Commission through the SPINE network in Europe. Such initiatives, essentially managed by large consortia, led to technology and method developments at the different steps required to produce biological samples compatible with structural studies. Besides specific applications, method developments resulted mainly upon miniaturization and parallelization. The challenge that academic laboratories faces to pursue structural genomics programs is to produce, at a higher rate, protein samples. The Structural Biology and Genomics Department (IGBMC - Illkirch - France) is implicated in a structural genomics program of high eukaryotes whose goal is solving crystal structures of proteins and their complexes (including large complexes) related to human health and biotechnology. To achieve such a challenging goal, the Department has established a medium-throughput pipeline for producing protein samples suitable for structural biology studies. Here, we describe the setting up of our initiative from cloning to crystallization and we demonstrate that structural genomics may be manageable by academic laboratories by strategic investments in robotic and by adapting classical bench protocols and new developments, in particular in the field of protein expression, to parallelization.
结构基因组学项目分布在世界各地,由美国国立卫生研究院(NIH)、日本理化学研究所(RIKEN)或欧盟委员会通过欧洲的SPINE网络等大型机构资助。这些项目主要由大型财团管理,在生产与结构研究兼容的生物样本所需的不同步骤中带来了技术和方法的发展。除了特定应用外,方法的发展主要源于小型化和平行化。学术实验室在开展结构基因组学项目时面临的挑战是更快地生产蛋白质样本。结构生物学与基因组学系(法国伊尔基希市IGBMC)参与了一个高等真核生物的结构基因组学项目,其目标是解析与人类健康和生物技术相关的蛋白质及其复合物(包括大型复合物)的晶体结构。为实现这一具有挑战性的目标,该系建立了一个中等通量的流程来生产适合结构生物学研究的蛋白质样本。在此,我们描述了从克隆到结晶的项目设置过程,并证明通过对机器人技术进行战略投资,以及调整经典的实验台操作流程和新进展,特别是在蛋白质表达领域,使其适应平行化,学术实验室可以开展结构基因组学研究。