Michelland Sylvie, Bourgoin-Voillard Sandrine, Cunin Valérie, Tollance Axel, Bertolino Pascal, Slais Karel, Seve Michel
Univ. Grenoble Alpes, Inserm, U1055, LBFA and BEeSy, PROMETHEE Proteomic Platform, Grenoble, France.
CHU de Grenoble, Institut de Biologie et de Pathologie, PROMETHEE Proteomic Platform, Grenoble, France.
Electrophoresis. 2017 Aug;38(16):2034-2041. doi: 10.1002/elps.201700075. Epub 2017 Jul 26.
High-throughput mass spectrometry-based proteomic analysis requires peptide fractionation to simplify complex biological samples and increase proteome coverage. OFFGEL fractionation technology became a common method to separate peptides or proteins using isoelectric focusing in an immobilized pH gradient. However, the OFFGEL focusing process may be further optimized and controlled in terms of separation time and pI resolution. Here we evaluated OFFGEL technology to separate peptides from different samples in the presence of low-molecular-weight (LMW) color pI markers to visualize the focusing process. LMW color pI markers covering a large pH range were added to the peptide mixture before OFFGEL fractionation using a 24-wells device encompassing the pH range 3-10. We also explored the impact of LMW color pI markers on peptide fractionation labeled previously for iTRAQ. Then, fractionated peptides were separated by RP_HPLC prior to MS analysis using MALDI-TOF/TOF mass spectrometry in MS and MS/MS modes. Here we report the performance of the peptide focusing process in the presence of LMW color pI markers as on-line trackers during the OFFGEL process and the possibility to use them as pI controls for peptide focusing. This method improves the workflow for peptide fractionation in a bottom-up proteomic approach with or without iTRAQ labeling.
基于高通量质谱的蛋白质组学分析需要进行肽段分级分离,以简化复杂的生物样品并提高蛋白质组覆盖率。非凝胶等电聚焦分级分离技术成为一种利用固定化pH梯度中的等电聚焦来分离肽段或蛋白质的常用方法。然而,非凝胶等电聚焦过程在分离时间和pI分辨率方面可能还需要进一步优化和控制。在此,我们评估了非凝胶等电聚焦技术,即在存在低分子量(LMW)彩色pI标记物的情况下,从不同样品中分离肽段,以可视化聚焦过程。在使用涵盖pH范围为3至10的24孔装置进行非凝胶等电聚焦分级分离之前,将覆盖较大pH范围的低分子量彩色pI标记物添加到肽混合物中。我们还探究了低分子量彩色pI标记物对先前用iTRAQ标记的肽段分级分离的影响。然后,在使用基质辅助激光解吸电离飞行时间串联质谱仪(MALDI-TOF/TOF)以MS和MS/MS模式进行质谱分析之前,通过反相高效液相色谱(RP-HPLC)分离分级后的肽段。在此,我们报告了在非凝胶等电聚焦过程中,低分子量彩色pI标记物作为在线追踪器时肽段聚焦过程的性能,以及将它们用作肽段聚焦的pI对照的可能性。该方法改进了自下而上蛋白质组学方法中肽段分级分离的工作流程,无论是否进行iTRAQ标记。