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. 2020 Jun 26;21:47. doi: 10.1186/s12860-020-00288-9

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© The Author(s) 2020

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 — Enrichment of cell surface proteins using the AOB labelling approach. a Distribution of the 723 unique proteins identified in this study between untreated (control) and cytokine-exposed equine articular chondrocytes. b Of the 723 unique proteins reliably identified in this study, 431 proteins were PM proteins (60%) according to UniProt database entries and gene ontology (GO) annotations. c Distribution of the 431 unique cell surface proteins identified in this study between untreated (control) and cytokine-exposed equine articular chondrocytes