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甲醛固定有助于在单细胞蛋白质组学样本处理和分析过程中保持蛋白质组状态。

Formaldehyde Fixation Helps Preserve the Proteome State during Single-Cell Proteomics Sample Processing and Analysis.

作者信息

Piga Ilaria, Koenig Claire, Lechner Maico, Sabatier Pierre, Olsen Jesper V

机构信息

Novo Nordisk Foundation Center for Protein Research, Proteomics Program, Faculty of Health and Medical Sciences, University of Copenhagen, 2200 Copenhagen, Denmark.

Cardio-Thoracic Translational Medicine (CTTM) Lab, Department of Surgical Sciences, Uppsala University, 753 10 Uppsala, Sweden.

出版信息

J Proteome Res. 2025 Apr 4;24(4):1624-1635. doi: 10.1021/acs.jproteome.4c00656. Epub 2025 Feb 3.

Abstract

Mass spectrometry-based single-cell proteomics (SCP) is gaining momentum but remains limited to a few laboratories due to the high costs and specialized expertise required. The ability to send samples to specialized core facilities would benefit nonspecialist laboratories and popularize SCP for biological applications. However, no methods have been tested in SCP to "freeze" the proteome state while maintaining cell integrity for transfer between laboratories or prolonged sorting using fluorescence-activated cell sorting (FACS). This study evaluates whether short-term formaldehyde (FA) fixation can maintain the cell states. We demonstrate that short-term FA fixation does not substantially affect protein recovery, even without heating and strong detergents, and maintains analytical depth compared with classical workflows. Fixation also preserves drug-induced specific perturbations of the protein abundance during cell sorting and sample preparation for SCP analysis. Our findings suggest that FA fixation can facilitate SCP by enabling sample shipping and prolonged sorting, potentially democratizing access to SCP technology and expanding its application in biological research, thereby accelerating discoveries in cell biology and personalized medicine.

摘要

基于质谱的单细胞蛋白质组学(SCP)正在兴起,但由于成本高昂且需要专业知识,目前仍仅限于少数实验室。将样本送到专业核心设施的能力将使非专业实验室受益,并使SCP在生物学应用中得到更广泛的应用。然而,在SCP中尚未测试过在保持细胞完整性以用于实验室间转移或使用荧光激活细胞分选(FACS)进行长时间分选的同时“冻结”蛋白质组状态的方法。本研究评估短期甲醛(FA)固定是否能维持细胞状态。我们证明,即使不加热和使用强力去污剂,短期FA固定也不会对蛋白质回收率产生实质性影响,并且与传统工作流程相比能保持分析深度。在进行SCP分析的细胞分选和样品制备过程中,固定还能保留药物诱导的蛋白质丰度的特定扰动。我们的研究结果表明,FA固定可以通过实现样本运输和长时间分选来促进SCP,有可能使SCP技术的获取更加普及,并扩大其在生物学研究中的应用,从而加速细胞生物学和个性化医学领域的发现。

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本文引用的文献

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