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. 2021 Nov 8;12(11):1059. doi: 10.1038/s41419-021-04317-z

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© The Author(s) 2021

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/.

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Fig. 6 — A Venn diagram of total proteins identified in necroptotic EVs compared with the published tumor neoantigens from B16F10, CT26, 4T1 models or CT26 in silico prediction [58]. TBQ EV-enriched proteins with FDR cutoff of 0.2 are marked with *. Fold change (FC) and Q-value are mentioned for each. B Violin plots showing log₂-LFQ intensity of the TBQ EV-enriched proteins annotated as the enriched GO biological process “antigen processing and presentation via MHC class I”. Q-value is mentioned individually above each plot, ^*Q < 0.1, ^**Q < 0.05. EVs, extracellular vesicles; FDR, false discovery rate; FC, fold change; TBQ, TNF-α, Birinapant, and QVD-OPh; GO, gene ontology; LFQ, label-free quantification; MHC, major histocompatibility complex.