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A tissue-based draft map of the murine MHC class I immunopeptidome

The large array of peptides presented to CD8+ T cells by major histocompatibility complex (MHC) class I molecules is referred to as the MHC class I immunopeptidome. Although the MHC class I immunopeptidome is ubiquitous in mammals and represents a critical component of the immune system, very little...

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Autores principales: Schuster, Heiko, Shao, Wenguang, Weiss, Tobias, Pedrioli, Patrick G.A., Roth, Patrick, Weller, Michael, Campbell, David S., Deutsch, Eric W., Moritz, Robert L., Planz, Oliver, Rammensee, Hans-Georg, Aebersold, Ruedi, Caron, Etienne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6080492/
https://www.ncbi.nlm.nih.gov/pubmed/30084848
http://dx.doi.org/10.1038/sdata.2018.157
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author Schuster, Heiko
Shao, Wenguang
Weiss, Tobias
Pedrioli, Patrick G.A.
Roth, Patrick
Weller, Michael
Campbell, David S.
Deutsch, Eric W.
Moritz, Robert L.
Planz, Oliver
Rammensee, Hans-Georg
Aebersold, Ruedi
Caron, Etienne
author_facet Schuster, Heiko
Shao, Wenguang
Weiss, Tobias
Pedrioli, Patrick G.A.
Roth, Patrick
Weller, Michael
Campbell, David S.
Deutsch, Eric W.
Moritz, Robert L.
Planz, Oliver
Rammensee, Hans-Georg
Aebersold, Ruedi
Caron, Etienne
author_sort Schuster, Heiko
collection PubMed
description The large array of peptides presented to CD8+ T cells by major histocompatibility complex (MHC) class I molecules is referred to as the MHC class I immunopeptidome. Although the MHC class I immunopeptidome is ubiquitous in mammals and represents a critical component of the immune system, very little is known, in any species, about its composition across most tissues and organs in vivo. We applied mass spectrometry (MS) technologies to draft the first tissue-based atlas of the murine MHC class I immunopeptidome in health. Peptides were extracted from 19 normal tissues from C57BL/6 mice and prepared for MS injections, resulting in a total number of 28,448 high-confidence H2D(b)/K(b)-associated peptides identified and annotated in the atlas. This atlas provides initial qualitative data to explore the tissue-specificity of the immunopeptidome and serves as a guide to identify potential tumor-associated antigens from various cancer models. Our data were shared via PRIDE (PXD008733), SysteMHC Atlas (SYSMHC00018) and SWATH Atlas. We anticipate that this unique dataset will be expanded in the future and will find wide applications in basic and translational immunology.
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spelling pubmed-60804922018-08-16 A tissue-based draft map of the murine MHC class I immunopeptidome Schuster, Heiko Shao, Wenguang Weiss, Tobias Pedrioli, Patrick G.A. Roth, Patrick Weller, Michael Campbell, David S. Deutsch, Eric W. Moritz, Robert L. Planz, Oliver Rammensee, Hans-Georg Aebersold, Ruedi Caron, Etienne Sci Data Data Descriptor The large array of peptides presented to CD8+ T cells by major histocompatibility complex (MHC) class I molecules is referred to as the MHC class I immunopeptidome. Although the MHC class I immunopeptidome is ubiquitous in mammals and represents a critical component of the immune system, very little is known, in any species, about its composition across most tissues and organs in vivo. We applied mass spectrometry (MS) technologies to draft the first tissue-based atlas of the murine MHC class I immunopeptidome in health. Peptides were extracted from 19 normal tissues from C57BL/6 mice and prepared for MS injections, resulting in a total number of 28,448 high-confidence H2D(b)/K(b)-associated peptides identified and annotated in the atlas. This atlas provides initial qualitative data to explore the tissue-specificity of the immunopeptidome and serves as a guide to identify potential tumor-associated antigens from various cancer models. Our data were shared via PRIDE (PXD008733), SysteMHC Atlas (SYSMHC00018) and SWATH Atlas. We anticipate that this unique dataset will be expanded in the future and will find wide applications in basic and translational immunology. Nature Publishing Group 2018-08-07 /pmc/articles/PMC6080492/ /pubmed/30084848 http://dx.doi.org/10.1038/sdata.2018.157 Text en Copyright © 2018, The Author(s) http://creativecommons.org/licenses/by/4.0/ Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ The Creative Commons Public Domain Dedication waiver http://creativecommons.org/publicdomain/zero/1.0/ applies to the metadata files made available in this article.
spellingShingle Data Descriptor
Schuster, Heiko
Shao, Wenguang
Weiss, Tobias
Pedrioli, Patrick G.A.
Roth, Patrick
Weller, Michael
Campbell, David S.
Deutsch, Eric W.
Moritz, Robert L.
Planz, Oliver
Rammensee, Hans-Georg
Aebersold, Ruedi
Caron, Etienne
A tissue-based draft map of the murine MHC class I immunopeptidome
title A tissue-based draft map of the murine MHC class I immunopeptidome
title_full A tissue-based draft map of the murine MHC class I immunopeptidome
title_fullStr A tissue-based draft map of the murine MHC class I immunopeptidome
title_full_unstemmed A tissue-based draft map of the murine MHC class I immunopeptidome
title_short A tissue-based draft map of the murine MHC class I immunopeptidome
title_sort tissue-based draft map of the murine mhc class i immunopeptidome
topic Data Descriptor
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6080492/
https://www.ncbi.nlm.nih.gov/pubmed/30084848
http://dx.doi.org/10.1038/sdata.2018.157
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