单细胞蛋白质组学的数据采集方法。

IF 3.4 4区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS Proteomics Pub Date : 2024-08-01 DOI:10.1002/pmic.202400022
Gautam Ghosh, Ariana E Shannon, Brian C Searle
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引用次数: 0

摘要

单细胞蛋白质组学(Single-cell proteomics,SCP)旨在表征单个细胞的蛋白质组,从而深入了解复杂的生物系统。它揭示了大量蛋白质组分析可能忽略的不同细胞群的细微差别,这对于了解疾病机制和开发靶向疗法至关重要。SCP 中的质谱(MS)方法可对单个细胞中的数千种蛋白质进行鉴定和定量。SCP 面临两大挑战:一是单细胞样本中的物质有限,需要高灵敏度的分析技术;二是样本的高效处理,因为每个生物样本需要进行数千次单细胞测量。本综述讨论了利用数据依赖性采集(DDA)和数据无关性采集(DIA)来减轻这些挑战的 MS 先进技术。此外,我们还探讨了使用短液相色谱梯度和样品复用方法来提高样品吞吐量和 SCP 实验的可扩展性。我们相信,这些方法将为我们更好地理解细胞异质性及其对系统生物学的影响铺平道路。
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Data acquisition approaches for single cell proteomics.

Single-cell proteomics (SCP) aims to characterize the proteome of individual cells, providing insights into complex biological systems. It reveals subtle differences in distinct cellular populations that bulk proteome analysis may overlook, which is essential for understanding disease mechanisms and developing targeted therapies. Mass spectrometry (MS) methods in SCP allow the identification and quantification of thousands of proteins from individual cells. Two major challenges in SCP are the limited material in single-cell samples necessitating highly sensitive analytical techniques and the efficient processing of samples, as each biological sample requires thousands of single cell measurements. This review discusses MS advancements to mitigate these challenges using data-dependent acquisition (DDA) and data-independent acquisition (DIA). Additionally, we examine the use of short liquid chromatography gradients and sample multiplexing methods that increase the sample throughput and scalability of SCP experiments. We believe these methods will pave the way for improving our understanding of cellular heterogeneity and its implications for systems biology.

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来源期刊
Proteomics
Proteomics 生物-生化研究方法
CiteScore
6.30
自引率
5.90%
发文量
193
审稿时长
3 months
期刊介绍: PROTEOMICS is the premier international source for information on all aspects of applications and technologies, including software, in proteomics and other "omics". The journal includes but is not limited to proteomics, genomics, transcriptomics, metabolomics and lipidomics, and systems biology approaches. Papers describing novel applications of proteomics and integration of multi-omics data and approaches are especially welcome.
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