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. 2021 Feb 9;19:42. doi: 10.1186/s12951-021-00785-9

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© The Author(s) 2021

Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 3 — In vitro binding studies. a Affinity/kinetics surface plasmon resonance study of SNA006a interacting with immobilized recombinant human CD8 protein. b The uptake of ¹²⁵I-SNA006 in MC38-CD8 (CD8-positive) and MC38 (CD8-negative) cells at 4 h. c The saturation binding curve of ¹²⁵I-SNA006 to MC38-CD8 cells at 4 h. d The competition binding curve of ¹²⁵I-SNA006 to MC38-CD8 cells at 4 h