Multi-laboratory experiment PME11 for the standardization of phosphoproteome analysis

dc.contributor.author
Colomé, Núria
dc.contributor.author
Abián, Joaquín
dc.contributor.author
Aloria, Kerman
dc.contributor.author
Arizmendi, Jesús M.
dc.contributor.author
Barceló Batllori, Sílvia
dc.contributor.author
Braga Lagache, Sophie
dc.contributor.author
Burlet Schiltz, Odile
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Carrascal, Montse
dc.contributor.author
Casal, J. Ignacio
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Chicano Gálvez, Eduard
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Chiva, Cristina
dc.contributor.author
Clemente, Luis Felipe
dc.contributor.author
Elortza, Felix
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Estanyol i Ullate, Josep Maria
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Fernandez Irigoyen, Joaquín
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Fernández Puente, Patricia
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Fidalgo, María José
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Froment, Carine
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Fuentes, Manuel
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Fuentes Almagro, Carlos
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Gay, Marina
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Hainard, Alexandre
dc.contributor.author
Heller, Manfred
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Hernández, María Luisa
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Ibarrola, Nieves
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Iloro, Ibon
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Kieselbach, Thomas
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Lario, Antonio
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Locard Paulet, Marie
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Marina Ramírez, Anabel
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Martín, Luna
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Morato López, Esperanza
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Muñoz, Javier
dc.contributor.author
Navajas, Rosana
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Odena, M. Antonia
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Odriozola, Leticia
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Oliveira, Eliandre
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Paradela, Alberto
dc.contributor.author
Pasquarello Mosimann, Carla
dc.contributor.author
Rios, Vivian de los
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Ruiz Romero, Cristina
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Sabidó Aguadé, Eduard
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Sánchez del Pino, Manuel
dc.contributor.author
Sancho, Jaime
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Santamaría, Enrique
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Schaeffer Reiss, Christine
dc.contributor.author
Schneider, Justine
dc.contributor.author
Torre, Carolina de la
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Valero, M. Luz
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Vilaseca, Marta
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Wu, Shuai
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Wu, Linfeng
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Ximénez Embún, Pilar
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Canals, Francesc
dc.contributor.author
Corrales, Fernando
dc.date.issued
2021-12-13T11:51:13Z
dc.date.issued
2021-12-13T11:51:13Z
dc.date.issued
2021-11-01
dc.date.issued
2021-12-10T09:25:45Z
dc.identifier
1874-3919
dc.identifier
https://hdl.handle.net/2445/181798
dc.identifier
34758407
dc.description.abstract
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.
dc.format
6 p.
dc.format
application/pdf
dc.language
eng
dc.publisher
Elsevier BV
dc.relation
Reproducció del document publicat a: https://doi.org/10.1016/j.jprot.2021.104409
dc.relation
Journal of Proteomics, 2021, vol. 251
dc.relation
https://doi.org/10.1016/j.jprot.2021.104409
dc.rights
cc by (c) Colomé, Núria et al, 2021
dc.rights
http://creativecommons.org/licenses/by/3.0/es/
dc.rights
info:eu-repo/semantics/openAccess
dc.source
Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))
dc.subject
Proteòmica
dc.subject
Normalització
dc.subject
Proteomics
dc.subject
Standardization
dc.title
Multi-laboratory experiment PME11 for the standardization of phosphoproteome analysis
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion


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