使用多段喷雾-毛细管CE-MS对picogram复杂样品进行高通量自上而下的蛋白质组学分析。

IF 6.7 1区 化学 Q1 CHEMISTRY, ANALYTICAL
Zhitao Zhao, , , Yanting Guo, , , Kellye A. Cupp-Sutton, , , Zhige Wang, , , Xiaowen Liu, , and , Si Wu*, 
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引用次数: 0

摘要

超灵敏的自上而下的蛋白质组学技术提供了有价值的见解ptm调节的细胞功能在质量有限的样品。毛细管电泳(CE)与传统的液相色谱(LC)方法相比,具有分辨率高、灵敏度高、循环时间短等优点,是一种很有前途的自上而下蛋白质组学分离技术。我们最近开发了“喷雾-毛细管”,这是一种用于定量超低体积采样和在线CE-MS分析的esi辅助设备,它成功地表征了数百种来自picogram细胞裂解物样品的完整蛋白质形态,并显示出对质量有限的复杂生物样品进行定量分析的前景。在本研究中,我们通过将多片段样品注射与我们的喷雾-毛细管CE-MS分析平台相结合,进一步提高了质量限制的自上而下蛋白质组学的通量。通过优化样品塞之间的间隔,我们能够在单个CE-MS分析之前将多个样品注射到喷雾毛细管中,从而实现来自不同片段的相同蛋白质的基线分离。在优化条件下,对ede进行量化。在单次分析(例如,运行时间约60分钟)中使用六点校准曲线共溶物(10-250 pg),产生强线性相关性(R2 > 0.98)。我们的方法每次运行最多支持17个样本段(例如,运行时间约90分钟),同时保持基线分离。这种优化的多段注射平台有潜力每天分析数百个质量有限的样品(例如,单细胞),显著提高自上而下蛋白质组学的通量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

High-Throughput Top-Down Proteomic Analysis of Picogram-Level Complex Samples Using Multisegment Spray-Capillary CE-MS

High-Throughput Top-Down Proteomic Analysis of Picogram-Level Complex Samples Using Multisegment Spray-Capillary CE-MS

Ultrasensitive top-down proteomics techniques provide valuable insights into PTM-regulated cellular functions in mass-limited samples. Capillary electrophoresis (CE) is a promising separation technique for top-down proteomics due to its high resolution, high sensitivity, and short cycle times compared to traditional liquid chromatography (LC)-based methods. We recently developed the “Spray-Capillary,” an ESI-assisted device for quantitative ultralow-volume sampling and online CE-MS analysis, which successfully characterized hundreds of intact proteoforms from picogram-level cell lysate samples and showed promise for quantitative analysis of mass-limited complex biological samples. In this study, we further improved throughput for mass-limited top-down proteomics by integrating multisegment sample injection with our spray-capillary CE-MS analysis platform. By optimizing the spacer between sample plugs, we enabled the injection of multiple samples into the spray-capillary prior to a single CE-MS analysis, achieving baseline separation of identical proteins from different segments. Under optimized conditions, we quantifiedE. colilysate (10–250 pg) using a six-point calibration curve in a single analysis (e.g., ∼60 min run time), yielding a strong linear correlation (R2 > 0.98). Our method supports up to 17 sample segments per run (e.g., ∼90 min run time) while maintaining baseline separation. This optimized multisegment injection platform has the potential to analyze hundreds of mass-limited samples (e.g., single cells) per day, significantly enhancing throughput in top-down proteomics.

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来源期刊
Analytical Chemistry
Analytical Chemistry 化学-分析化学
CiteScore
12.10
自引率
12.20%
发文量
1949
审稿时长
1.4 months
期刊介绍: Analytical Chemistry, a peer-reviewed research journal, focuses on disseminating new and original knowledge across all branches of analytical chemistry. Fundamental articles may explore general principles of chemical measurement science and need not directly address existing or potential analytical methodology. They can be entirely theoretical or report experimental results. Contributions may cover various phases of analytical operations, including sampling, bioanalysis, electrochemistry, mass spectrometry, microscale and nanoscale systems, environmental analysis, separations, spectroscopy, chemical reactions and selectivity, instrumentation, imaging, surface analysis, and data processing. Papers discussing known analytical methods should present a significant, original application of the method, a notable improvement, or results on an important analyte.
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