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. 2024 May 10;15:3969. doi: 10.1038/s41467-024-48287-0

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© The Author(s) 2024

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 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/.

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Fig. 7 — TRIF, p.R841 WWP2, and p.R841H WWP2 were in vitro translated. An in vitro ubiquitination assay of TRIF was conducted by using an E1 ubiquitin-activating enzyme and UbcH5c together with either p.R841 WWP2 or p.R841H WWP2. Ubiquitin-conjugated TRIF was detected by immunoblot with an anti-ubiquitin antibody. The expression levels of WWP2 were also verified by immunoblots with an anti-WWP2 antibody. Results represent 1 experiment among 2.