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. 2017 May 2;7:1370. doi: 10.1038/s41598-017-01409-9

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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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The redox status of cellular organelles in A431 cells subjected to the different Photofrin-PDT regimens. The proteins corresponding to the quantified Met-peptides (oxidized or reduced) were assigned to their known subcellular locations using GO analysis, and the log2 (PDT/Ctrl) ratio distributions of all oxidized (left panels) and reduced (right panels) Met-peptides were analyzed for each cellular site/organelle under each PDT condition. The box representations are the same as in Fig. 4. The numbers of oxidized (or reduced) Met-peptides grouped and analyzed in each cellular site/organelle are shown below each box. The top three most severely oxidized cellular structures in each PDT condition are indicated by 1, 2 and 3 in left panels.