Kim Ki Hun, Compton Philip D, Tran John C, Kelleher Neil L
Departments of Chemistry and Molecular Biosciences and the Proteomics Center of Excellence, Northwestern University, 2145 North Sheridan Road, Evanston, Illinois 60208, United States.
J Proteome Res. 2015 May 1;14(5):2199-206. doi: 10.1021/pr501331q. Epub 2015 Apr 15.
A fractionation method called gel-eluted liquid fraction entrapment electrophoresis (GELFrEE) has been used to dramatically increase the number of proteins identified in top-down proteomic workflows; however, the technique involves the use of sodium dodecyl sulfate (SDS), a surfactant that interferes with electrospray ionization. Therefore, an efficient removal of SDS is absolutely required prior to mass analysis. Traditionally, methanol/chloroform precipitation and spin columns have been used, but they lack reproducibility and are difficult to automate. Therefore, we developed an in-line matrix removal platform to enable the direct analysis of samples containing SDS and salts. Only small molecules like SDS permeate a porous membrane and are removed in a manner similar to cross-flow filtration. With this device, near-complete removal of SDS is accomplished within 5 min and proteins are subsequently mobilized into a mass spectrometer. The new platform was optimized for the analysis of GELFrEE fractions enriched for histones extracted from human HeLa cells. All four core histones and their proteoforms were detected in a single spectrum by high-resolution mass spectrometry. The new method versus protein precipitation/resuspension showed 2- to 10-fold improved signal intensities, offering a clear path forward to improve proteome coverage and the efficiency of top-down proteomics.
一种称为凝胶洗脱液相截留电泳(GELFrEE)的分级分离方法已被用于显著增加自上而下蛋白质组学工作流程中鉴定出的蛋白质数量;然而,该技术涉及使用十二烷基硫酸钠(SDS),一种会干扰电喷雾电离的表面活性剂。因此,在进行质谱分析之前,必须有效去除SDS。传统上,使用甲醇/氯仿沉淀和离心柱,但它们缺乏重现性且难以自动化。因此,我们开发了一种在线基质去除平台,以实现对含有SDS和盐的样品的直接分析。只有像SDS这样的小分子能够渗透过多孔膜,并以类似于错流过滤的方式被去除。使用该装置,能在5分钟内几乎完全去除SDS,随后蛋白质被转移到质谱仪中。这个新平台针对从人HeLa细胞中提取的富含组蛋白的GELFrEE级分的分析进行了优化。通过高分辨率质谱在单个光谱中检测到了所有四种核心组蛋白及其蛋白变体。与蛋白质沉淀/重悬法相比,新方法的信号强度提高了2至10倍,为提高蛋白质组覆盖率和自上而下蛋白质组学的效率提供了一条清晰的前进道路。