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. 2022 Jan 27;7:13. doi: 10.1038/s41541-022-00430-y

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© This is a U.S. government work and not under copyright protection in the U.S.; foreign copyright protection may apply 2022

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. 5 — A, D, G Rosetta predicted monomer structures of TMV-Junc-NPNAx5, TMV-RI, and TMV-NPNAx20. Images were generated using PyMOL. B, E, H Left panels show coomassie blue-stained SDS-PAGE gel bands (arrows) of Nickel and Q-Sepharose purified proteins; right panels show electron micrographs for each antigen. C ELISA reactivity curves of TMV-Junc-NPNAx5 binding to mAb CIS43, mAb 317, or PBS control. F Western blot using Region I specific mAb 5D5 against TMV-RI and FL-CSP antigen. I Representative ELISA curves of TMV-NPNAx20 and TMV-NPNAx5 reactivity to mAb 580 and mAb 317.