Kinoshita Eiji, Kinoshita-Kikuta Emiko, Ujihara Hiromi, Koike Tohru
Department of Functional Molecular Science, Graduate School of Biomedical Sciences, Hiroshima University, Hiroshima 734-8553, Japan.
Proteomics. 2009 Aug;9(16):4098-101. doi: 10.1002/pmic.200900020.
We describe a novel technique of phosphate-affinity SDS-PAGE using Phos-tag to analyze large phosphoproteins with molecular masses of more than 200 kDa. The protein phosphoisotypes were clearly separated as up-shifted migration bands in a 3% w/v polyacrylamide gel containing 20 microM Phos-tag and 0.5% w/v agarose. In subsequent immunoblotting, the procedure permitted the determination of the phosphoisotypes of high-molecular-mass proteins, such as mTOR (289 kDa), ATM kinase (350 kDa), and 53BP1 (213 kDa).
我们描述了一种使用Phos-tag进行磷酸盐亲和SDS-PAGE的新技术,用于分析分子量超过200 kDa的大型磷酸化蛋白质。在含有20 microM Phos-tag和0.5% w/v琼脂糖的3% w/v聚丙烯酰胺凝胶中,蛋白质磷酸异构体以向上迁移的条带形式清晰分离。在随后的免疫印迹中,该方法可用于测定高分子量蛋白质的磷酸异构体,如mTOR(289 kDa)、ATM激酶(350 kDa)和53BP1(213 kDa)。