Thermo Fisher Scientific, Dornierstrasse 4, 82110 Germering, Germany.
IMP─Institute of Molecular Pathology, Campus-Vienna-Biocenter 1, A-1030 Vienna, Austria.
J Proteome Res. 2022 Oct 7;21(10):2545-2551. doi: 10.1021/acs.jproteome.2c00270. Epub 2022 Sep 6.
This study demonstrates how the latest ultrahigh-performance liquid chromatography (UHPLC) technology can be combined with high-resolution accurate-mass (HRAM) mass spectrometry (MS) and long columns packed with fully porous particles to improve bottom-up proteomics analysis with nanoflow liquid chromatography-mass spectrometry (nanoLC-MS) methods. The increased back pressures from the UHPLC system enabled the use of 75 μm I.D. × 75 cm columns packed with 2 μm particles at a typical 300 nL/min flow rate as well as elevated and reduced flow rates. The constant pressure pump operation at 1500 bar reduced sample loading and column washing/equilibration stages and overall overhead time, which maximizes MS utilization time. The versatility of flow rate optimization to balance the sensitivity, throughput with sample loading amount, and capability of using longer gradients contributes to a greater number of peptide and protein identifications for single-shot bottom-up proteomics experiments. The routine proteome profiling and precise quantification of >7000 proteins with single-shot nanoLC-MS analysis open possibilities for large-scale discovery studies with a deep dive into the protein level alterations. Data are available via ProteomeXchange with identifier PXD035665.
本研究展示了如何将最新的超高效液相色谱 (UHPLC) 技术与高分辨率精确质量 (HRAM) 质谱 (MS) 和填充全多孔颗粒的长柱相结合,以改进基于纳升液相色谱-质谱 (nanoLC-MS) 方法的自上而下的蛋白质组学分析。来自 UHPLC 系统的增加的背压允许在典型的 300 nL/min 流速下使用 75 μm ID × 75 cm 柱,柱中填充 2 μm 颗粒,以及升高和降低流速。在 1500 bar 下的恒压泵操作减少了样品加载和柱洗涤/平衡阶段以及总体开销时间,从而最大限度地利用了 MS 时间。通过优化流速来平衡灵敏度、样品加载量的通量以及使用更长梯度的能力,实现了单次自上而下蛋白质组学实验中更多肽和蛋白质的鉴定。通过单次 nanoLC-MS 分析对>7000 种蛋白质进行常规蛋白质组分析和精确定量,为深入研究蛋白质水平的变化提供了大规模发现研究的可能性。数据可通过 ProteomeXchange 以标识符 PXD035665 获得。