<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>6</volume><submitter>Ebstein F</submitter><pubmed_abstract>Proteasome-catalyzed peptide splicing represents an additional catalytic activity of proteasomes contributing to the pool of MHC-class I-presented epitopes. We here biochemically and functionally characterized a new melanoma gp100 derived spliced epitope. We demonstrate that the gp100(mel)47-52/40-42 antigenic peptide is generated in vitro and in cellulo by a not yet described proteasomal condensation reaction. gp100(mel)47-52/40-42 generation is enhanced in the presence of the β5i/LMP7 proteasome-subunit and elicits a peptide-specific CD8(+) T cell response. Importantly, we demonstrate that different gp100(mel)-derived spliced epitopes are generated and presented to CD8(+) T cells with efficacies comparable to non-spliced canonical tumor epitopes and that gp100(mel)-derived spliced epitop</pubmed_abstract><journal>Scientific reports</journal><pagination>24032</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4822137</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Proteasomes generate spliced epitopes by two different mechanisms and as efficiently as non-spliced epitopes.</pubmed_title><pmcid>PMC4822137</pmcid><pubmed_authors>Textoris-Taube K</pubmed_authors><pubmed_authors>Schadendorf D</pubmed_authors><pubmed_authors>Henklein P</pubmed_authors><pubmed_authors>Van den Eynde BJ</pubmed_authors><pubmed_authors>Uckert W</pubmed_authors><pubmed_authors>Urban S</pubmed_authors><pubmed_authors>Vigneron N</pubmed_authors><pubmed_authors>Golnik R</pubmed_authors><pubmed_authors>Mishto M</pubmed_authors><pubmed_authors>Keller C</pubmed_authors><pubmed_authors>Albrecht-Koepke N</pubmed_authors><pubmed_authors>Ebstein F</pubmed_authors><pubmed_authors>Janek K</pubmed_authors><pubmed_authors>Kloetzel PM</pubmed_authors><pubmed_authors>Lorenz FK</pubmed_authors><pubmed_authors>Schuler-Thurner B</pubmed_authors><pubmed_authors>Niewienda A</pubmed_authors><pubmed_authors>Lehmann A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Proteasomes generate spliced epitopes by two different mechanisms and as efficiently as non-spliced epitopes.</name><description>Proteasome-catalyzed peptide splicing represents an additional catalytic activity of proteasomes contributing to the pool of MHC-class I-presented epitopes. We here biochemically and functionally characterized a new melanoma gp100 derived spliced epitope. We demonstrate that the gp100(mel)47-52/40-42 antigenic peptide is generated in vitro and in cellulo by a not yet described proteasomal condensation reaction. gp100(mel)47-52/40-42 generation is enhanced in the presence of the β5i/LMP7 proteasome-subunit and elicits a peptide-specific CD8(+) T cell response. Importantly, we demonstrate that different gp100(mel)-derived spliced epitopes are generated and presented to CD8(+) T cells with efficacies comparable to non-spliced canonical tumor epitopes and that gp100(mel)-derived spliced epitop</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Apr</publication><modification>2025-04-04T23:50:55.556Z</modification><creation>2019-03-27T03:11:18Z</creation></dates><accession>S-EPMC4822137</accession><cross_references><pubmed>27049119</pubmed><doi>10.1038/srep24032</doi></cross_references></HashMap>