Laboratory of Pathology, Centre for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Laboratory of Cell Biology, Centre for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Biosensors (Basel). 2020 Oct 31;10(11):160. doi: 10.3390/bios10110160.
Sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) is a widely utilized technique for macromolecule and protein analysis. While multiple methods exist to visualize the separated protein bands on gels, one of most popular methods of staining the proteins is with Coomassie dye. A more recent approach is to use Bio-Rad stain-free technology for visualizing protein bands with UV light and achieve similar or greater sensitivity than that of Coomassie dye. Here, we developed a method to further amplify the sensitivity of stain-free gels using carboxyfluorescein succinimidyl ester (CFSE) staining. We compared our novel method using foetal bovine serum samples with Coomassie dye, standard stain-free gels, and silver staining. Our results show that while silver staining remains a gold-standard method in terms of sensitivity; CFSE staining of samples prior to use with stain-free gels results in a 10-100-fold increase in sensitivity over Coomassie staining and the standard stain-free method. Our method offers a sensitivity similar to that of silver staining which is compatible with downstream mass spectrometry, and therefore more advantageous for further retrieval and analysis of macromolecules in bands.
十二烷基硫酸钠聚丙烯酰胺凝胶电泳(SDS-PAGE)是一种广泛用于分析大分子和蛋白质的技术。虽然有多种方法可以在凝胶上可视化分离的蛋白质条带,但最受欢迎的蛋白质染色方法之一是考马斯亮蓝染料。最近的一种方法是使用 Bio-Rad 的无染技术,通过紫外线对蛋白质条带进行可视化,并实现与考马斯亮蓝染料相似或更高的灵敏度。在这里,我们开发了一种使用羧基荧光素琥珀酰亚胺酯(CFSE)染色进一步提高无染凝胶灵敏度的方法。我们将我们的新方法与考马斯亮蓝染料、标准无染凝胶和银染进行了比较。我们的结果表明,虽然银染在灵敏度方面仍然是一种金标准方法;但在使用无染凝胶之前对样品进行 CFSE 染色,与考马斯亮蓝染色和标准无染方法相比,灵敏度可提高 10-100 倍。我们的方法提供了类似于银染的灵敏度,与下游质谱兼容,因此更有利于进一步检索和分析条带中的大分子。