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. 2021 Apr 12;12:2173. doi: 10.1038/s41467-021-22359-x

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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. 4 — Binding of KIR2DL2 and 2DL3 tetramers to a panel of 97 HLA class I molecules. a Shown as a heatmap by mean fluorescence intensity and percentage of maximum HLA-I ligand binding. b KIR2DL2 and c 2DL3 binding to individual HLA-I beads represented in bar format with errors displayed as standard deviation. HLA are categorised by KIR-binding epitope, HLA-C1 (cyan), HLA-C2 (dark blue), HLA A3/A11 (red). All data are representative of three independent experiments. The top 21 HLA ligands above background are shown. Error bars are shown as mean with SD.