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Título

Deepening into intracellular signaling landscape through integrative spatial proteomics and transcriptomics in a lymphoma model

AutorLandeira-Viñuela, Alicia; Díez, Paula; Juanes-Velasco, Pablo; Lécrevisse, Quentin; Orfao, Alberto CSIC ORCID ; De Las Rivas, Javier CSIC ORCID CVN ; Fuentes, Manuel CSIC ORCID
Palabras claveAffinity-based proteomics
Human proteome project
LC-MS/MS
Transcriptomics
Size-exclusion-chromatography
Fecha de publicación2021
EditorMultidisciplinary Digital Publishing Institute
CitaciónBiomolecules 11(12): 1776 (2021)
ResumenHuman Proteome Project (HPP) presents a systematic characterization of the protein landscape under different conditions using several complementary-omic techniques (LC-MS/MS proteomics, affinity proteomics, transcriptomics, etc.). In the present study, using a B-cell lymphoma cell line as a model, comprehensive integration of RNA-Seq transcriptomics, MS/MS, and antibody-based affinity proteomics (combined with size-exclusion chromatography) (SEC-MAP) were performed to uncover correlations that could provide insights into protein dynamics at the intracellular level. Here, 5672 unique proteins were systematically identified by MS/MS analysis and subcellular protein extraction strategies (neXtProt release 2020-21, MS/MS data are available via ProteomeXchange with identifier PXD003939). Moreover, RNA deep sequencing analysis of this lymphoma B-cell line identified 19,518 expressed genes and 5707 protein coding genes (mapped to neXtProt). Among these data sets, 162 relevant proteins (targeted by 206 antibodies) were systematically analyzed by the SEC-MAP approach, providing information about PTMs, isoforms, protein complexes, and subcellular localization. Finally, a bioinformatic pipeline has been designed and developed for orthogonal integration of these high-content proteomics and transcriptomics datasets, which might be useful for comprehensive and global characterization of intracellular protein profiles.
Descripción© 2021 by the authors.
Versión del editorhttp://dx.doi.org/10.3390/biom11121776
URIhttp://hdl.handle.net/10261/261324
DOI10.3390/biom11121776
E-ISSN2218-273X
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