Schafer Frank, Römer Ulla, Emmerlich Melanie, Blümer Julia, Lubenow Helge, Steinert Kerstin
QIAGEN GmbH, Hilden, Germany.
J Biomol Tech. 2002 Sep;13(3):131-42.
Methods based on immobilized-metal affinity chromatography (IMAC) technology for the isolation of 6xHis-tagged proteins offer a one-step purification process that is both robust and meets the challenge of quantitatively purifying thousands of proteins with differing structures and characteristics. To perform this method in a high-throughput, automated format, protocols have been developed that can be run on lab automation workstations. Ready-to-run protocols covering a wide range of protein purification and assay applications, and which rely on the well-established 6xHis-Ni-NTA IMAC technology, are available. An Ni-NTA magnetic bead-based protocol allows micro-scale purification of up to 15 microg of 6xHis-tagged protein per well. If larger amounts of purified protein are needed, a vacuum-controlled Ni-NTA resin-based process provides a convenient medium-scale method for purification of up to 300 microg of 6xHis-tagged protein in a 96-well format. This protocol has been adapted to further increase the yield of 6xHis-tagged proteins allowing purification of up to several milligrams of highly pure protein per well. The protocol can process 96 samples, each derived from up to 25 mL culture volume (E. coli), in less than 3 h. Examples of purification and assay applications using the protocols mentioned above, and data on reproducibility and cross-contamination-free processing are shown.
基于固定化金属亲和色谱(IMAC)技术分离6xHis标签蛋白的方法提供了一种一步纯化过程,该过程既稳健,又能应对定量纯化数千种具有不同结构和特性的蛋白的挑战。为了以高通量、自动化形式执行此方法,已开发出可在实验室自动化工作站上运行的方案。现已有涵盖广泛蛋白质纯化和检测应用的即用型方案,这些方案依赖成熟的6xHis-Ni-NTA IMAC技术。基于Ni-NTA磁珠的方案允许在每孔中微量纯化多达15微克的6xHis标签蛋白。如果需要更大量的纯化蛋白,基于真空控制的Ni-NTA树脂的方法提供了一种方便的中规模方法,可在96孔板中纯化多达300微克的6xHis标签蛋白。此方案已进行调整以进一步提高6xHis标签蛋白的产量,从而允许每孔纯化多达数毫克的高纯度蛋白。该方案可在不到3小时内处理96个样品,每个样品最多来自25毫升培养体积(大肠杆菌)。展示了使用上述方案进行纯化和检测应用的示例,以及关于重现性和无交叉污染处理的数据。