Gatti A, Traugh J A
Department of Biochemistry, University of California, Riverside, California, 92521,
Anal Biochem. 1999 Jan 15;266(2):198-204. doi: 10.1006/abio.1998.2955.
A novel two-dimensional electrophoresis system to be carried out on polyacrylamide gels under nondenaturing conditions was developed to efficiently fractionate the peptides resulting from endoproteinase digestion of 32P-labeled proteins. In particular, nondenaturing gel isoelectric focusing was combined with alkaline 40% polyacrylamide gel electrophoresis to generate phosphopeptide maps with high reproducibility, thus allowing both protein fingerprinting and comparative analysis of different samples. The potential application of this method for subsequent amino acid sequencing of the isolated phosphopeptides was further demonstrated by successful manual and automated Edman sequencing. Taken together these data show that such a simple and precise approach is suitable for both analytical and preparative aims.
开发了一种新型二维电泳系统,该系统在非变性条件下于聚丙烯酰胺凝胶上进行,以有效分离32P标记蛋白质经内蛋白酶消化产生的肽段。具体而言,非变性凝胶等电聚焦与碱性40%聚丙烯酰胺凝胶电泳相结合,以生成具有高重现性的磷酸肽图谱,从而实现蛋白质指纹识别以及不同样品的比较分析。通过成功的手动和自动埃德曼测序进一步证明了该方法在后续分离的磷酸肽氨基酸测序中的潜在应用。综合这些数据表明,这种简单而精确的方法适用于分析和制备目的。