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. 2016 Oct 24;16:231. doi: 10.1186/s12870-016-0920-3

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© The Author(s). 2016

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 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.

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Fig. 2 — Functional distribution of proteins identified in Clematis terniflora DC. leaves. C. terniflora leaves were collected pre- and post-treatment with high level of UV-B irradiation for 5 h followed by dark for 36 h. Proteins within the leaves were identified using a 2-DE gel proteomic technique based on MALDI-TOF-MS/MS. The function of each identified protein was predicated and categorized using MapMan bin codes. Numbers of categorized proteins are shown in the graph. Red bars indicate increased proteins post-treatment compared with pre-treatment, and black bars indicate decreased. Abbreviations: CHO, carbohydrate; TCA, tricarboxylic acid