作者
Hamish Stewart,Dmitry Grinfeld,Anastassios E. Giannakopulos,J. Petzoldt,Toby Shanley,Matthew Garland,Eduard Denisov,Amelia C. Peterson,Eugen Damoc,Martin Zeller,Tabiwang N. Arrey,Anna Pashkova,Santosh Renuse,Amirmansoor Hakimi,Andreas Kühn,Matthias Biel,Arne Kreutzmann,Bernd Hagedorn,Immo Colonius,Alexander Schütz,Arne Stefes,Ankit Dwivedi,Daniel Mourad,Max Hoek,Bastian Reitemeier,Philipp Cochems,Alexander Kholomeev,Robert Ostermann,Gregor Quiring,Maximilian Ochmann,S.A.I. Mohring,Alexander Wagner,André Petker,Sebastian Kanngiesser,Michael Wiedemeyer,Wilko Balschun,Daniel J. Hermanson,Vlad Zabrouskov,Alexander Makarov,Christian Hock
摘要
The growing trend toward high-throughput proteomics demands rapid liquid chromatography-mass spectrometry (LC-MS) cycles that limit the available time to gather the large numbers of MS/MS fragmentation spectra required for identification. Orbitrap analyzers scale performance with acquisition time and necessarily sacrifice sensitivity and resolving power to deliver higher acquisition rates. We developed a new mass spectrometer that combines a mass-resolving quadrupole, the Orbitrap, and the novel Asymmetric Track Lossless (Astral) analyzer. The new hybrid instrument enables faster acquisition of high-resolution accurate mass (HRAM) MS/MS spectra compared with state-of-the-art mass spectrometers. Accordingly, new proteomics methods were developed that leverage the strengths of each HRAM analyzer, whereby the Orbitrap analyzer performs full scans with a high dynamic range and resolution, synchronized with the Astral analyzer's acquisition of fast and sensitive HRAM MS/MS scans. Substantial improvements are demonstrated over previous methods using current state-of-the-art mass spectrometers.