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单细胞蛋白质组学的新进展。

What's new in single-cell proteomics.

作者信息

Truong Thy, Kelly Ryan T

机构信息

Department of Chemistry and Biochemistry, Brigham Young University, Provo, UT 84602, United States.

Department of Chemistry and Biochemistry, Brigham Young University, Provo, UT 84602, United States.

出版信息

Curr Opin Biotechnol. 2024 Apr;86:103077. doi: 10.1016/j.copbio.2024.103077. Epub 2024 Feb 14.

Abstract

In recent years, single-cell proteomics (SCP) has advanced significantly, enabling the analysis of thousands of proteins within single mammalian cells. This progress is driven by advances in experimental design, with maturing label-free and multiplexed methods, optimized sample preparation, and innovations in separation techniques, including ultra-low-flow nanoLC. These factors collectively contribute to improved sensitivity, throughput, and reproducibility. Cutting-edge mass spectrometry platforms and data acquisition approaches continue to play a critical role in enhancing data quality. Furthermore, the exploration of spatial proteomics with single-cell resolution offers significant promise for understanding cellular interactions, giving rise to various phenotypes. SCP has far-reaching applications in cancer research, biomarker discovery, and developmental biology. Here, we provide a critical review of recent advances in the field of SCP.

摘要

近年来,单细胞蛋白质组学(SCP)取得了显著进展,能够对单个哺乳动物细胞内的数千种蛋白质进行分析。这一进展得益于实验设计的进步,包括无标记和多重方法的成熟、优化的样品制备以及分离技术的创新,如超低流量纳升液相色谱。这些因素共同提高了灵敏度、通量和重现性。前沿的质谱平台和数据采集方法在提高数据质量方面继续发挥着关键作用。此外,具有单细胞分辨率的空间蛋白质组学探索为理解细胞间相互作用带来了巨大希望,从而产生各种表型。SCP在癌症研究、生物标志物发现和发育生物学中具有深远的应用。在此,我们对SCP领域的最新进展进行批判性综述。

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