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. 2017 Aug 31;7:10281. doi: 10.1038/s41598-017-09926-3

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© The Author(s) 2017

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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Comparative analysis of exoproteomes of PAK and PAK/pJN-FcsR by 2D DIGE. (a) Multiple images for one DIGE gel showing spot profiles for PAK (Cy3 labeled, green), PAK/pJN-FcsR (Cy5 labeled, red) and internal standard (Cy2 labeled, blue). (b) Overlay image of PAK (green) and PAK/pJN-FcsR (red) channels. Differential spots between strains (considering all four DIGE gels, p-values ≤ 0.05 and fold change ≥ 25%) are indicated and were further identified by MS analysis. Protein identities, fold changes and p values are listed in Supplementary Table S4. (c) 3D view of selected spots with significant normalized abundance fold changes: spot 1 CdrA (fold change 4.1) spot 4 flagellar hook-associated protein (fold change 11.2) and spot 7 flagellin (fold change 15.2).