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MHC Class I Immunopeptidome: Past, Present, and Future

In the 35 years since the revelation that short peptides bound to major histocompatibility complex class I and II molecules are the secret of the major histocompatibility complex–restricted nature of T-cell recognition, there has been enormous progress in characterizing the immunopeptidome, the repe...

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Autor principal: Yewdell, Jonathan W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9243166/
https://www.ncbi.nlm.nih.gov/pubmed/35395404
http://dx.doi.org/10.1016/j.mcpro.2022.100230
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author Yewdell, Jonathan W.
author_facet Yewdell, Jonathan W.
author_sort Yewdell, Jonathan W.
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description In the 35 years since the revelation that short peptides bound to major histocompatibility complex class I and II molecules are the secret of the major histocompatibility complex–restricted nature of T-cell recognition, there has been enormous progress in characterizing the immunopeptidome, the repertoire of peptide presented for immunosurveillance. Here, the major milestones in the journey are marked, the contribution of proteasome-mediated splicing to the immunopeptidome is discussed, and exciting recent findings relating the immunopeptidome to the translatome revealed by ribosome profiling (RiboSeq) is detailed. Finally, what is needed for continued progress is opined about, which includes the infusion of talented young scientists into the antigen-processing field, currently undergoing a renaissance; thanks in part to the astounding success of T-cell–based cancer immunotherapy.
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spelling pubmed-92431662022-07-01 MHC Class I Immunopeptidome: Past, Present, and Future Yewdell, Jonathan W. Mol Cell Proteomics Perspective In the 35 years since the revelation that short peptides bound to major histocompatibility complex class I and II molecules are the secret of the major histocompatibility complex–restricted nature of T-cell recognition, there has been enormous progress in characterizing the immunopeptidome, the repertoire of peptide presented for immunosurveillance. Here, the major milestones in the journey are marked, the contribution of proteasome-mediated splicing to the immunopeptidome is discussed, and exciting recent findings relating the immunopeptidome to the translatome revealed by ribosome profiling (RiboSeq) is detailed. Finally, what is needed for continued progress is opined about, which includes the infusion of talented young scientists into the antigen-processing field, currently undergoing a renaissance; thanks in part to the astounding success of T-cell–based cancer immunotherapy. American Society for Biochemistry and Molecular Biology 2022-04-05 /pmc/articles/PMC9243166/ /pubmed/35395404 http://dx.doi.org/10.1016/j.mcpro.2022.100230 Text en © 2022 The Author https://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 Perspective
Yewdell, Jonathan W.
MHC Class I Immunopeptidome: Past, Present, and Future
title MHC Class I Immunopeptidome: Past, Present, and Future
title_full MHC Class I Immunopeptidome: Past, Present, and Future
title_fullStr MHC Class I Immunopeptidome: Past, Present, and Future
title_full_unstemmed MHC Class I Immunopeptidome: Past, Present, and Future
title_short MHC Class I Immunopeptidome: Past, Present, and Future
title_sort mhc class i immunopeptidome: past, present, and future
topic Perspective
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9243166/
https://www.ncbi.nlm.nih.gov/pubmed/35395404
http://dx.doi.org/10.1016/j.mcpro.2022.100230
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