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

Ulises H. Guzmán(University of Copenhagen), Ana Martínez‐Val(University of Copenhagen), Zilu Ye(University of Copenhagen), Eugen Damoc(Thermo Fisher Scientific (Germany)), Tabiwang N. Arrey(Thermo Fisher Scientific (Germany)), Anna Pashkova(Thermo Fisher Scientific (Germany)), Santosh Renuse(Thermo Fisher Scientific (United States)), Eduard Denisov(Thermo Fisher Scientific (Germany)), J. Petzoldt(Thermo Fisher Scientific (Germany)), Amelia C. Peterson(Thermo Fisher Scientific (Germany)), Florian Harking(University of Copenhagen), Ole Østergaard(University of Copenhagen), Rasmus Rydbirk(University of Southern Denmark), Susana Aznar(Copenhagen University Hospital), Hamish Stewart(Thermo Fisher Scientific (Germany)), Yue Xuan(Thermo Fisher Scientific (Germany)), Daniel Hermanson(Thermo Fisher Scientific (United States)), Stevan Horning(Thermo Fisher Scientific (Germany)), Christian Hock(Thermo Fisher Scientific (Germany)), Alexander Makarov(Thermo Fisher Scientific (Germany)), Vlad Zabrouskov(Thermo Fisher Scientific (United States)), Jesper V. Olsen(University of Copenhagen)
Nature Biotechnology
February 1, 2024
Cited by 319Open Access
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Abstract

Mass 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.


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