Ultra-fast label-free quantification and comprehensive proteome coverage with narrow-window data-independent acquisition

Author:

Guzman Ulises H.ORCID,Martinez-Val AnaORCID,Ye ZiluORCID,Damoc Eugen,Arrey Tabiwang N.,Pashkova Anna,Renuse Santosh,Denisov Eduard,Petzoldt Johannes,Peterson Amelia C.,Harking Florian,Østergaard OleORCID,Rydbirk RasmusORCID,Aznar SusanaORCID,Stewart Hamish,Xuan YueORCID,Hermanson Daniel,Horning Stevan,Hock Christian,Makarov AlexanderORCID,Zabrouskov Vlad,Olsen Jesper V.ORCID

Abstract

AbstractMass spectrometry (MS)-based proteomics aims to characterize comprehensive proteomes in a fast and reproducible manner. Here we present the narrow-window data-independent acquisition (nDIA) strategy consisting of high-resolution MS1 scans with parallel tandem MS (MS/MS) scans of ~200 Hz using 2-Th 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 which provides >200-Hz MS/MS scanning speed, high resolving power and sensitivity, and low-ppm mass accuracy. The nDIA strategy enables profiling of >100 full yeast proteomes per day, or 48 human proteomes per day at the depth of ~10,000 human protein groups in half-an-hour or ~7,000 proteins in 5 min, representing 3× higher coverage compared with current state-of-the-art MS. Multi-shot acquisition of offline fractionated samples provides comprehensive coverage of human proteomes in ~3 h. High quantitative precision and accuracy are demonstrated in a three-species proteome mixture, quantifying 14,000+ protein groups in a single half-an-hour run.

Publisher

Springer Science and Business Media LLC

Subject

Biomedical Engineering,Molecular Medicine,Applied Microbiology and Biotechnology,Bioengineering,Biotechnology

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. A new mass analyzer shakes up the proteomics field;Nature Biotechnology;2024-02-01

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