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. 2018 Nov 6;9:4634. doi: 10.1038/s41467-018-07009-z

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© The Author(s) 2018

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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Fig. 1 — Proteomic analysis of POD machinery and identification of DYNAMO1. a Phase contrast (PC) and immunofluorescence images of C. merolae cells during G1 phase, anaphase, and cytokinesis. Ps peroxisome (anti-catalase antibody), Dnm1 (anti-Dnm1 antibody). b Schematic representing isolation and proteomic analysis of POD machinery. Nu cell nucleus, Mito mitochondrion, Pt plastid, Mito div. mitochondrial division period, Ps div peroxisomal division period. c Upper panel shows the 0.8% OG-treated POD machinery fraction and the lower panel shows the 0.2% LDAO-treated POD machinery fraction. d Typical structures of isolated POD machinery stained with the anti-Dnm1 antibody. e LC–ESI–MS/MS analysis of the nucleoside diphosphate kinase activity of recombinant DYNAMO1. f Schematic representing a working model of nucleoside diphosphate kinase. Data in e are means ± s.d. (n = 3). Scale bars: 1 μm (a, upper panels); 500 nm (a, lower panels; c, d)