Fast and Deep Phosphoproteome Analysis with the Orbitrap Astral Mass Spectrometer

Author:

Lancaster Noah M.ORCID,Sinitcyn PavelORCID,Forny PatrickORCID,Peters-Clarke Trenton M.ORCID,Fecher CarolineORCID,Smith Andrew J.ORCID,Shishkova EvgeniaORCID,Arrey Tabiwang N.,Pashkova Anna,Robinson Margaret LeaORCID,Arp NicholasORCID,Fan JingORCID,Hansen Juli,Galmozzi AndreaORCID,Serrano Lia R.ORCID,Westphall Michael S.ORCID,Stewart HamishORCID,Hock Christian,Damoc EugenORCID,Pagliarini David J.ORCID,Zabrouskov VladORCID,Coon Joshua J.ORCID

Abstract

ABSTRACTOwing to its roles in cellular signal transduction, protein phosphorylation plays critical roles in myriad cell processes. That said, detecting and quantifying protein phosphorylation has remained a challenge. We describe the use of a novel mass spectrometer (Orbitrap Astral) coupled with data-independent acquisition (DIA) to achieve rapid and deep analysis of human and mouse phosphoproteomes. With this method we map approximately 30,000 unique human phosphorylation sites within a half-hour of data collection. We applied this approach to generate a phosphoproteome multi-tissue atlas of the mouse. Altogether, we detected 81,120 unique phosphorylation sites within 12 hours of measurement. With this unique dataset, we examine the sequence and structural context of protein phosphorylation. Finally, we highlight the discovery potential of this resource with multiple examples of novel phosphorylation events relevant to mitochondrial and brain biology.

Publisher

Cold Spring Harbor Laboratory

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