Show simple item record

dc.contributor.authorProteoRed-ISCIII
dc.contributor.authorEuPA
dc.contributor.authorAloria Escolastico, Kerman
dc.contributor.authorArizmendi Bastarrika, Jesús María ORCID
dc.contributor.authorElortza, Felix
dc.date.accessioned2022-01-28T09:15:45Z
dc.date.available2022-01-28T09:15:45Z
dc.date.issued2022-01-16
dc.identifier.citationJournal of Proteomics 251 : (2022) // Article ID 104409es_ES
dc.identifier.issn1874-3919
dc.identifier.issn1876-7737
dc.identifier.urihttp://hdl.handle.net/10810/55187
dc.description.abstract[EN] 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.es_ES
dc.description.sponsorshipWe thank Kevin Ray from MilliporeSigma, Saint Louis, MO, for fruitful discussions on the study design, and MilliporeSigma for kindly providing the Phosphomix standards used in the study. ProteoRed, PRB3 is supported by grant PT17/0019/0001, of the PE I+D+i 2013-2016, funded by ISCIII and ERDF.es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.subjectquality controles_ES
dc.subjectenrichmentes_ES
dc.titleMulti-laboratory experiment PME11 for the standardization of phosphoproteome analysises_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holder© 2021 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).es_ES
dc.rights.holderAtribución 3.0 España*
dc.relation.publisherversionhttps://www.sciencedirect.com/science/article/pii/S1874391921003080?via%3Dihubes_ES
dc.identifier.doi10.1016/j.jprot.2021.104409
dc.departamentoesBioquímica y biología moleculares_ES
dc.departamentoeuBiokimika eta biologia molekularraes_ES


Files in this item

Thumbnail
Thumbnail

This item appears in the following Collection(s)

Show simple item record

© 2021 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
Except where otherwise noted, this item's license is described as © 2021 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).