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. 2023 Jan 2;41(7):932–943. doi: 10.1038/s41587-022-01567-w

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© The Author(s) 2023

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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Extended Data Fig. 4 — a NY-ESO1 yeast clones (WT, N1, N4 & N5) were stained with serial diluted NY-ESO1/HLA-A*02:01. The numbers of AlexaFluor 647 positive cells with different NY-ESO1/HLA-A*02:01 concentration are shown as mean±s.d. (n = 3 biological replicates). b MART1 yeast clones (MA2 & MA5) were stained with serial diluted MART1/HLA-A*02:01. The numbers of AlexaFluor 647 positive cells with different MART1/HLA-A*02:01 concentration are shown as mean±s.d. (n = 3 biological replicates). c GP100 yeast clones (gp1 & gp11) were stained with serial diluted GP100/HLA-A*02:01. The numbers of AlexaFluor 647 positive cells with different GP100/HLA-A*02:01concentration are shown as mean±s.d. (n = 3 biological replicates). d KRAS yeast clones (RAS1 & RAS2) were stained with serial diluted KRAS/HLA-A*02:01. The numbers of AlexaFluor 647 positive cells with different KRAS/HLA-A*02:01 concentration are shown as mean±s.d. (n = 3 biological replicates).

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