Single-cell proteomics using mass spectrometry.

IF 11.1 Q1 CELL BIOLOGY
Cell genomics Pub Date : 2025-09-10 Epub Date: 2025-08-20 DOI:10.1016/j.xgen.2025.100973
Amanda Momenzadeh, Jesse G Meyer
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引用次数: 0

Abstract

Over the past 2 to 3 years, mass-spectrometry-based single-cell proteomics (SCP) has experienced transformative improvements in microfluidic and robotic sample preparation, innovative MS1- and MS2-based multiplexing strategies, and specialized hardware (e.g., timsTOF Ultra 2, Astral), which have dramatically boosted sensitivity, throughput, and proteome coverage from picogram-level protein inputs. Concurrently, tailored computational workflows that encompass normalization, imputation, and no-code platforms have addressed pervasive missing data challenges and standardized analyses, collectively enabling high-throughput, reproducible profiling of cellular heterogeneity. This minireview summarizes the latest progress in SCP technology and software solutions, highlighting how the closer integration of analytical, computational, and experimental strategies will facilitate a deeper and broader coverage of single-cell proteomes.

单细胞蛋白质组学使用质谱法。
在过去的2到3年中,基于质谱的单细胞蛋白质组学(SCP)在微流体和机器人样品制备,创新的基于MS1和ms2的多路复用策略以及专门的硬件(例如,timsTOF Ultra 2, Astral)方面经历了变革性的改进,这些改进极大地提高了灵敏度,吞吐量和蛋白质组覆盖从皮克级蛋白质输入。同时,量身定制的计算工作流程,包括标准化、归一化和无代码平台,解决了普遍存在的缺失数据挑战和标准化分析,共同实现了高通量、可重复的细胞异质性分析。这篇综述总结了SCP技术和软件解决方案的最新进展,强调了分析、计算和实验策略的紧密结合将如何促进单细胞蛋白质组学更深入、更广泛的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.10
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0.00%
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