Vincentelli Renaud, Canaan Stéphane, Offant Julien, Cambillau Christian, Bignon Christophe
Architecture et Fonction des Macromolécules Biologiques, UMR 6098, CNRS/Universités d'Aix-Marseille I et II, Case 932, 163 Avenue de Luminy, 13288 Marseille cedex 9, France.
Anal Biochem. 2005 Nov 1;346(1):77-84. doi: 10.1016/j.ab.2005.07.039. Epub 2005 Aug 15.
A growing need for sensitive and high-throughput methods for screening the expression and solubility of recombinant proteins exists in structural genomics. Originally, the emergency solution was to use immediately available techniques such as manual lysis of expression cells followed by analysis of protein expression by gel electrophoresis. However, these handmade methods quickly proved to be unfit for the high-throughput demand of postgenomics, and it is now generally accepted that the long-term solution to this problem will be based on automation, on industrial standard-formatted experiments, and on downsizing samples and consumables. In agreement with this consensus, we have set up a fully automated method based on a dot-blot technology and using 96-well format consumables for assessing by immunodetection the amount of total and soluble recombinant histidine (His)-tagged proteins expressed in Escherichia coli. The method starts with the harvest of expression cells and ends with the display of solubility/expression results in milligrams of recombinant protein per liter of culture using a three-color code to assist analysis. The program autonomously processes 160 independent cultures at a time.
结构基因组学领域对用于筛选重组蛋白表达和溶解性的灵敏且高通量方法的需求日益增长。最初,应急解决方案是使用现成的技术,如手动裂解表达细胞,然后通过凝胶电泳分析蛋白质表达。然而,这些手工方法很快被证明不适合后基因组学的高通量需求,现在人们普遍认为,解决这个问题的长期方案将基于自动化、工业标准格式的实验以及样品和耗材的小型化。与这一共识一致,我们建立了一种基于斑点印迹技术的全自动方法,使用96孔格式的耗材,通过免疫检测来评估在大肠杆菌中表达的重组组氨酸(His)标签蛋白的总量和可溶性。该方法从收获表达细胞开始,以使用三色编码辅助分析的每升培养物中重组蛋白毫克数的溶解性/表达结果展示结束。该程序一次可自主处理160个独立培养物。