In vivo identification of potential uranium protein targets in zebrafish ovaries after chronic waterborne exposure. Issue 5 (20th March 2017)

• Record Type: Journal Article
• Authors: Eb-Levadoux, Y.; Frelon, S.; Simon, O.; Arnaudguilhem, C.; Lobinski, R.; Mounicou, S.
• Is Part Of: Metallomics. Volume 9:Issue 5(2017)
• Page Start: 525
• Page End: 534
• Publication Date: 2017-03-20
• Subjects: Metals -- Physiological effect -- Periodicals; 572.51
• DOI: 10.1039/c6mt00291a
• Languages: English
• ISSNs: 1756-5901

Abstract

Abstract : To better understand uranium reprotoxicity mechanisms in zebrafish, potential protein targets likely to complex uranium in ovaries were identified and found to be involved in biological processes such as oxidation balance, cell and tissue structure and embryo early development. Abstract : Ecotoxicological studies have indicated the reprotoxicity of uranium (U) in zebrafish, but its molecular mechanisms remain unclear. Due to the non-covalent nature of U–protein complexes, canonical proteomics approaches are often not relevant as they usually use denaturating reagents or solvents. In this study, non-denaturating (ND) methods were used to obtain insight into the nature of U potential targets in ovaries of reproduced and non-reproduced zebrafish after 20 days of exposure to an environmentally relevant U concentration (20 μg L −1 ). After the ND sample preparation, 1-dimensional (SEC) and 2-dimensional (OGE × SEC) separations followed by ICP-sector-field MS measurements (U, P, Fe, Cu, and Zn) enabled the determination of chemical characteristics (MW, pI) of the metal–protein complexes. Phosphorus and U coelution confirmed the affinity of U for P-containing proteins. In addition, 2D separation allowed the discrimination of Fe-metalloproteins as potential U targets. Finally, 20 protein candidates for U complexation were identified after tryptic digestion conditions by LC-ESI FT MS and a database search. Potential U targets were mainly involved in three biological processes: oxidative stress regulation (SOD, GST), cytoskeleton structure (actin) and embryo early development (vtg, initiation factor).