Cappione Amedeo, Smith Janet, Mabuchi Masaharu, Nadler Timothy
EMD Millipore, Merck KGaA, 17 Cherry Hill Drive, Danvers, MA 01923, USA.
Int J Proteomics. 2012;2012:473843. doi: 10.1155/2012/473843. Epub 2012 Aug 15.
Expression profiling on a large scale, as is the case in drug discovery, is often accomplished through use of sophisticated solid-phase protein microarrays or multiplex bead technologies. While offering both high-throughput and high-content analysis, these platforms are often too cost prohibitive or technically challenging for many research settings. Capitalizing on the favorable attributes of the standard ELISA and slot blotting techniques, we developed a modified dot blot assay that provides a simple cost-effective alternative for semiquantitative expression analysis of multiple proteins across multiple samples. Similar in protocol to an ELISA, but based in a membrane bound 96-well microplate, the assay takes advantage of vacuum filtration to expedite the tedious process of washing in between binding steps. We report on the optimization of the assay and demonstrate its use in profiling temporal changes in phosphorylation events in the well-characterized EGF-induced signaling cascade of A431 cells.
在药物研发等大规模表达谱分析中,通常通过使用复杂的固相蛋白质微阵列或多重珠技术来完成。虽然这些平台提供了高通量和高内涵分析,但对于许多研究环境而言,它们往往成本过高或技术上具有挑战性。利用标准ELISA和狭缝印迹技术的有利特性,我们开发了一种改良的斑点印迹测定法,为跨多个样品的多种蛋白质的半定量表达分析提供了一种简单且经济高效的替代方法。该测定法在方案上与ELISA相似,但基于膜结合的96孔微孔板,利用真空过滤来加快结合步骤之间繁琐的洗涤过程。我们报告了该测定法的优化,并展示了其在分析A431细胞中充分表征的EGF诱导信号级联反应中磷酸化事件的时间变化中的应用。