蛋白质组
质谱法
定量蛋白质组学
轨道轨道
化学
蛋白质组学
多路复用
分析化学(期刊)
计算机科学
色谱法
生物信息学
生物
生物化学
基因
作者
Ulises H. Guzman,Ana Martínez-Val,Zilu Ye,Eugen Damoc,Tabiwang N. Arrey,Anna Pashkova,Eduard Denisov,J. Petzoldt,Amelia C. Peterson,Florian S. Harking,Ole Østergaard,Hamish Stewart,Yue Xuan,Daniel J. Hermanson,Christian Hock,Alexander Makarov,Vlad Zabrouskov,Jesper V. Olsen
标识
DOI:10.1101/2023.06.02.543374
摘要
Abstract Mass spectrometry (MS)-based proteomics aims to characterize comprehensive proteomes in a fast and reproducible manner. Here, we present an ultra-fast scanning data-independent acquisition (DIA) strategy consisting on 2-Th precursor isolation windows, dissolving the differences between data-dependent and independent methods. This is achieved by pairing a Quadrupole Orbitrap mass spectrometer with the asymmetric track lossless (Astral) analyzer that provides >200 Hz MS/MS scanning speed, high resolving power and sensitivity, as well as low ppm-mass accuracy. Narrow-window DIA enables profiling of up to 100 full yeast proteomes per day, or ∼10,000 human proteins in half-an-hour. Moreover, multi-shot acquisition of fractionated samples allows comprehensive coverage of human proteomes in ∼3h, showing comparable depth to next-generation RNA sequencing and with 10x higher throughput compared to current state-of-the-art MS. High quantitative precision and accuracy is demonstrated with high peptide coverage in a 3-species proteome mixture, quantifying 14,000+ proteins in a single run in half-an-hour. Teaser Accurate and precise label-free quantification with comprehensive proteome coverage using narrow-window DIA
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