开发高效、有效、经济的蛋白质组分析技术。

IF 4.3 Q1 BIOCHEMICAL RESEARCH METHODS Cell Reports Methods Pub Date : 2024-06-17 Epub Date: 2024-06-11 DOI:10.1016/j.crmeth.2024.100796
Katherine R Martin, Ha T Le, Ahmed Abdelgawad, Canyuan Yang, Guotao Lu, Jessica L Keffer, Xiaohui Zhang, Zhihao Zhuang, Papa Nii Asare-Okai, Clara S Chan, Mona Batish, Yanbao Yu
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引用次数: 0

摘要

我们提出了一种高效、有效、经济的蛋白质组学样品制备方法,命名为 E3 技术。通过将二氧化硅微颗粒固定在聚四氟乙烯基质中,我们开发出了一种坚固的膜介质,它可以作为一种可靠的平台,以快速、低成本的方式生成蛋白质组学友好型样品。我们使用不同的格式对其性能进行了基准测试,并通过各种复杂程度、数量和体积的样品类型进行了演示。我们的数据表明,E3 技术的蛋白质组鉴定和定量性能相当于或优于许多现有方法。我们进一步提出了一种增强型单血管方法,命名为 E4 技术,它能在滤器上进行细胞内消化,样品损失极少,灵敏度高,从而实现了低投入和低细胞蛋白质组学。最后,我们利用上述技术研究了 RNA 结合蛋白和完整细菌细胞蛋白质组。
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Development of an efficient, effective, and economical technology for proteome analysis.

We present an efficient, effective, and economical approach, named E3technology, for proteomics sample preparation. By immobilizing silica microparticles into the polytetrafluoroethylene matrix, we develop a robust membrane medium, which could serve as a reliable platform to generate proteomics-friendly samples in a rapid and low-cost fashion. We benchmark its performance using different formats and demonstrate them with a variety of sample types of varied complexity, quantity, and volume. Our data suggest that E3technology provides proteome-wide identification and quantitation performance equivalent or superior to many existing methods. We further propose an enhanced single-vessel approach, named E4technology, which performs on-filter in-cell digestion with minimal sample loss and high sensitivity, enabling low-input and low-cell proteomics. Lastly, we utilized the above technologies to investigate RNA-binding proteins and profile the intact bacterial cell proteome.

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来源期刊
Cell Reports Methods
Cell Reports Methods Chemistry (General), Biochemistry, Genetics and Molecular Biology (General), Immunology and Microbiology (General)
CiteScore
3.80
自引率
0.00%
发文量
0
审稿时长
111 days
期刊最新文献
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