Development of an efficient, effective, and economical technology for proteome analysis.

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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Abstract

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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开发高效、有效、经济的蛋白质组分析技术。
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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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
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