Dorri Yaser
University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.
Methods Mol Biol. 2012;869:235-46. doi: 10.1007/978-1-61779-821-4_19.
Two-dimensional gel electrophoresis (2-DE) is one of the most powerful tools for separating proteins based on their size and charge. 2-DE is very useful to separate two proteins with identical molecular weights but different charges, which cannot be achieved with just sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE). Here, a simpler and easier version of 2-DE is presented which is also faster than all the currently available techniques. In this modified version of 2-DE, isoelectric focusing is carried out in the first dimension using a vertical SDS-PAGE apparatus. Following the first-dimensional IEF, each individual lane is excised from the IEF gel and, after a 90° rotation, is inserted into a second-dimensional SDS-PAGE, which can be stained with Coomassie Brilliant Blue for protein analysis or immunoblotted for further analysis. This version of IEF can be run in less than 2 h compared to the overnight run required by O'Farrell's method. Difficult tube gel casting and gel extrusion as well as tube gel distortion are eliminated in our method. This method is simpler, faster, and inexpensive. Both dimensions can be done on the same SDS-PAGE apparatus, and up to ten samples can be run simultaneously using one gel.
二维凝胶电泳(2-DE)是基于蛋白质大小和电荷分离蛋白质的最强大工具之一。2-DE对于分离分子量相同但电荷不同的两种蛋白质非常有用,而仅使用十二烷基硫酸钠聚丙烯酰胺凝胶电泳(SDS-PAGE)则无法实现这一点。在此,我们展示了一种更简单、更便捷的2-DE版本,其速度也比目前所有可用技术都要快。在这种改进的2-DE版本中,使用垂直SDS-PAGE装置在第一维进行等电聚焦。在一维IEF之后,从IEF凝胶中切下每个单独的泳道,旋转90°后,插入到二维SDS-PAGE中,可使用考马斯亮蓝染色进行蛋白质分析,或进行免疫印迹以进一步分析。与奥法雷尔方法所需的过夜运行相比,此版本的IEF运行时间可少于2小时。我们的方法消除了困难的管凝胶浇铸、凝胶挤出以及管凝胶变形问题。该方法更简单、更快且成本低廉。两个维度都可以在同一SDS-PAGE装置上完成,使用一块凝胶可同时运行多达十个样品。