Bjerneld Erik J, Johansson Johan D, Laurin Ylva, Hagner-McWhirter Åsa, Rönn Ola, Karlsson Robert
GE Healthcare Bio-Sciences, SE-751 84 Uppsala, Sweden.
GE Healthcare Bio-Sciences, SE-751 84 Uppsala, Sweden.
Anal Biochem. 2015 Sep 1;484:51-7. doi: 10.1016/j.ab.2015.04.036. Epub 2015 May 6.
A pre-labeling protocol based on Cy5 N-hydroxysuccinimide (NHS) ester labeling of proteins has been developed for one-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) analysis. We show that a fixed amount of sulfonated Cy5 can be used in the labeling reaction to label proteins over a broad concentration range-more than three orders of magnitude. The optimal amount of Cy5 was found to be 50 to 250pmol in 20μl using a Tris-HCl labeling buffer at pH 8.7. Labeling protein samples with a fixed amount of dye in this range balances the requirements of sub-nanogram detection sensitivity and low dye-to-protein (D/P) ratios for SDS-PAGE. Simulations of the labeling reaction reproduced experimental observations of both labeling kinetics and D/P ratios. Two-dimensional electrophoresis was used to examine the labeling of proteins in a cell lysate using both sulfonated and non-sulfonated Cy5. For both types of Cy5, we observed efficient labeling across a broad range of molecular weights and isoelectric points.
已开发出一种基于蛋白质的Cy5 N - 羟基琥珀酰亚胺(NHS)酯标记的预标记方案,用于一维十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳(SDS - PAGE)分析。我们表明,在标记反应中可以使用固定量的磺化Cy5在很宽的浓度范围内标记蛋白质——超过三个数量级。使用pH 8.7的Tris - HCl标记缓冲液时,发现20μl中Cy5的最佳量为50至250pmol。在此范围内用固定量的染料标记蛋白质样品,平衡了SDS - PAGE亚纳克检测灵敏度和低染料与蛋白质(D/P)比率的要求。标记反应的模拟重现了标记动力学和D/P比率的实验观察结果。二维电泳用于使用磺化和未磺化的Cy5检测细胞裂解物中蛋白质的标记情况。对于这两种类型的Cy5,我们观察到在很宽的分子量和等电点范围内都有高效标记。