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Data on interleukin (IL)-2- and IL-15-dependent changes in IL-2Rβ and IL-2Rγ complexes

We provide detailed datasets from our analysis of the proteins that associate with IL-2Rβ and IL-2Rγ in T-cells stimulated with IL-2 or IL-15 compared with resting T-cells, as identified by SILAC-based quantitative proteomics. We also include quantitative data regarding site-specific phosphorylation...

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Detalles Bibliográficos
Autores principales: Osinalde, Nerea, Sánchez-Quiles, Virginia, Blagoev, Blagoy, Kratchmarova, Irina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5345956/
https://www.ncbi.nlm.nih.gov/pubmed/28331895
http://dx.doi.org/10.1016/j.dib.2017.02.030
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author Osinalde, Nerea
Sánchez-Quiles, Virginia
Blagoev, Blagoy
Kratchmarova, Irina
author_facet Osinalde, Nerea
Sánchez-Quiles, Virginia
Blagoev, Blagoy
Kratchmarova, Irina
author_sort Osinalde, Nerea
collection PubMed
description We provide detailed datasets from our analysis of the proteins that associate with IL-2Rβ and IL-2Rγ in T-cells stimulated with IL-2 or IL-15 compared with resting T-cells, as identified by SILAC-based quantitative proteomics. We also include quantitative data regarding site-specific phosphorylation events observed both in IL-2Rβ and IL-2Rγ. Moreover, we provide results demonstrating the specific protein recruitment capacity of four of those site-specific phosphorylations. The proteomics and phosphoproteomics data described in this article is associated with a research article entitled “Characterization of receptor-associated protein complex assembly in Interleukin (IL)-2- and IL-15-activated T-lymphocytes” (Osinalde et al., 2016 [1]). The mass spectrometry data have been deposited to the ProteomeEXchange Constorium with the identifier PXD002386.
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spelling pubmed-53459562017-03-22 Data on interleukin (IL)-2- and IL-15-dependent changes in IL-2Rβ and IL-2Rγ complexes Osinalde, Nerea Sánchez-Quiles, Virginia Blagoev, Blagoy Kratchmarova, Irina Data Brief Data Article We provide detailed datasets from our analysis of the proteins that associate with IL-2Rβ and IL-2Rγ in T-cells stimulated with IL-2 or IL-15 compared with resting T-cells, as identified by SILAC-based quantitative proteomics. We also include quantitative data regarding site-specific phosphorylation events observed both in IL-2Rβ and IL-2Rγ. Moreover, we provide results demonstrating the specific protein recruitment capacity of four of those site-specific phosphorylations. The proteomics and phosphoproteomics data described in this article is associated with a research article entitled “Characterization of receptor-associated protein complex assembly in Interleukin (IL)-2- and IL-15-activated T-lymphocytes” (Osinalde et al., 2016 [1]). The mass spectrometry data have been deposited to the ProteomeEXchange Constorium with the identifier PXD002386. Elsevier 2017-03-02 /pmc/articles/PMC5345956/ /pubmed/28331895 http://dx.doi.org/10.1016/j.dib.2017.02.030 Text en © 2017 Published by Elsevier Inc. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Data Article
Osinalde, Nerea
Sánchez-Quiles, Virginia
Blagoev, Blagoy
Kratchmarova, Irina
Data on interleukin (IL)-2- and IL-15-dependent changes in IL-2Rβ and IL-2Rγ complexes
title Data on interleukin (IL)-2- and IL-15-dependent changes in IL-2Rβ and IL-2Rγ complexes
title_full Data on interleukin (IL)-2- and IL-15-dependent changes in IL-2Rβ and IL-2Rγ complexes
title_fullStr Data on interleukin (IL)-2- and IL-15-dependent changes in IL-2Rβ and IL-2Rγ complexes
title_full_unstemmed Data on interleukin (IL)-2- and IL-15-dependent changes in IL-2Rβ and IL-2Rγ complexes
title_short Data on interleukin (IL)-2- and IL-15-dependent changes in IL-2Rβ and IL-2Rγ complexes
title_sort data on interleukin (il)-2- and il-15-dependent changes in il-2rβ and il-2rγ complexes
topic Data Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5345956/
https://www.ncbi.nlm.nih.gov/pubmed/28331895
http://dx.doi.org/10.1016/j.dib.2017.02.030
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