Harper Sandra, W Speicher David
The Wistar Institute, Philadelphia, Pennsylvania.
Curr Protoc Protein Sci. 2019 Jun;96(1):e87. doi: 10.1002/cpps.87. Epub 2019 Mar 6.
This manuscript describes protocols for separation of complex protein samples using two-dimensional polyacrylamide gel electrophoresis (2D-PAGE). Electrophoresis in a single dimension, e.g., 1D SDS polyacrylamide gels, has the potential to rapidly separate hundreds of proteins. When two orthogonal high-resolution electrophoretic methods are efficiently combined in perpendicular dimensions, complex protein mixtures can be separated into thousands of discrete spots. The most common 2D gel separation for intact proteins involves a first-dimensional separation using isoelectric focusing (IEF) followed by separation based on protein size (SDS-PAGE). Currently, most 2D gel studies rely on the use of commercially available immobilized pH gradient (IPG) gels, which provide improved ease of use and reproducibility compared with older methods. IPG gels are available in a range of sizes and different pH ranges. Resolution typically increases as the 2D gel size increases; however, difficulty of use increases sharply and throughput decreases as gel size increases. © 2019 by John Wiley & Sons, Inc.
本手稿描述了使用二维聚丙烯酰胺凝胶电泳(2D-PAGE)分离复杂蛋白质样品的方法。一维电泳,例如一维SDS聚丙烯酰胺凝胶电泳,有可能快速分离数百种蛋白质。当两种正交的高分辨率电泳方法在垂直方向上有效结合时,复杂的蛋白质混合物可以被分离成数千个离散的斑点。完整蛋白质最常见的二维凝胶分离方法是首先使用等电聚焦(IEF)进行一维分离,然后基于蛋白质大小进行分离(SDS-PAGE)。目前,大多数二维凝胶研究依赖于使用市售的固定化pH梯度(IPG)凝胶,与旧方法相比,其使用更简便且重现性更好。IPG凝胶有多种尺寸和不同的pH范围可供选择。分辨率通常随着二维凝胶尺寸的增加而提高;然而,随着凝胶尺寸的增加,使用难度急剧增加,通量降低。© 2019 约翰威立父子公司版权所有