2026-04-17T11:55:42Zhttps://recercat.cat/oai/request

oai:recercat.cat:10230/528222025-12-12T01:32:59Zcom_2072_6col_2072_452952

00925njm 22002777a 4500 dc Colomé, Núria author Chiva, Cristina author Sabidó Aguadé, Eduard, 1981- author EuPA author 2022-04-04T06:31:21Z 2022-04-04T06:31:21Z 2022 Global analysis of protein phosphorylation by mass spectrometry proteomic techniques has emerged in the last decades as a powerful tool in biological and biomedical research. However, there are several factors that make the global study of the phosphoproteome more challenging than measuring non-modified proteins. The low stoichiometry of the phosphorylated species and the need to retrieve residue specific information require particular attention on sample preparation, data acquisition and processing to ensure reproducibility, qualitative and quantitative robustness and ample phosphoproteome coverage in phosphoproteomic workflows. Aiming to investigate the effect of different variables in the performance of proteome wide phosphoprotein analysis protocols, ProteoRed-ISCIII and EuPA launched the Proteomics Multicentric Experiment 11 (PME11). A reference sample consisting of a yeast protein extract spiked in with different amounts of a phosphomix standard (Sigma/Merck) was distributed to 31 laboratories around the globe. Thirty-six datasets from 23 laboratories were analyzed. Our results indicate the suitability of the PME11 reference sample to benchmark and optimize phosphoproteomics strategies, weighing the influence of different factors, as well as to rank intra and inter laboratory performance. Funding: ProteoRed, PRB3 is supported by grant PT17/0019/0001, of the PE I+D+i 2013-2016, funded by ISCIII and ERDF Fosforilació Fosfoproteïnes Proteòmica Multi-laboratory experiment PME11 for the standardization of phosphoproteome analysis