<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Cardozo G</submitter><funding>Espacio Interdisciplinario Universidad de la República Uruguay</funding><funding>Programa de Alimentos y Salud Humana (PAyS) IDB</funding><funding>Programa de Desarrollo de Ciencias Básicas</funding><funding>Espacio Interdisciplinario_2020 (to R.R.), Universidad de la República, Uruguay</funding><funding>Comisión Sectorial de Investigación Científica</funding><funding>Programa de Alimentos y Salud Humana (PAyS) Uruguay</funding><funding>Sistema Nacional de Investigadores</funding><funding>Comisión Sectorial de Investigación Científica Universidad de la República Uruguay</funding><pagination>408</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9952270</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(2)</volume><pubmed_abstract>Human peroxiredoxin 3 (&lt;i>Hs&lt;/i>Prx3) is a thiol-based peroxidase responsible for the reduction of most hydrogen peroxide and peroxynitrite formed in mitochondria. Mitochondrial disfunction can lead to membrane lipoperoxidation, resulting in the formation of lipid-bound fatty acid hydroperoxides (&lt;sub>L&lt;/sub>FA-OOHs) which can be released to become free fatty acid hydroperoxides (&lt;sub>f&lt;/sub>FA-OOHs). Herein, we report that &lt;i>Hs&lt;/i>Prx3 is oxidized and hyperoxidized by &lt;sub>f&lt;/sub>FA-OOHs including those derived from arachidonic acid and eicosapentaenoic acid peroxidation at position 15 with remarkably high rate constants of oxidation (>3.5 × 10&lt;sup>7&lt;/sup> M&lt;sup>-1&lt;/sup>s&lt;sup>-1&lt;/sup>) and hyperoxidation (~2 × 10&lt;sup>7&lt;/sup> M&lt;sup>-1&lt;/sup>s&lt;sup>-1&lt;/sup>). The endoperoxide-hydroperoxide P</pubmed_abstract><journal>Antioxidants (Basel, Switzerland)</journal><pubmed_title>Mitochondrial Peroxiredoxin 3 Is Rapidly Oxidized and Hyperoxidized by Fatty Acid Hydroperoxides.</pubmed_title><pmcid>PMC9952270</pmcid><funding_grant_id>CSIC_2018</funding_grant_id><funding_grant_id>IDB - R.O.U. (4950/OC-UR)</funding_grant_id><funding_grant_id>GID2018_34</funding_grant_id><funding_grant_id>4950/OC-UR</funding_grant_id><funding_grant_id>CSIC i+d 2020 257</funding_grant_id><funding_grant_id>Centros Interdisciplinarios 2020</funding_grant_id><funding_grant_id>I+D 2020</funding_grant_id><pubmed_authors>Cardozo G</pubmed_authors><pubmed_authors>Mastrogiovanni M</pubmed_authors><pubmed_authors>Trujillo M</pubmed_authors><pubmed_authors>Radi R</pubmed_authors><pubmed_authors>Viera N</pubmed_authors><pubmed_authors>Zeida A</pubmed_authors><pubmed_authors>Reyes AM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Mitochondrial Peroxiredoxin 3 Is Rapidly Oxidized and Hyperoxidized by Fatty Acid Hydroperoxides.</name><description>Human peroxiredoxin 3 (&lt;i>Hs&lt;/i>Prx3) is a thiol-based peroxidase responsible for the reduction of most hydrogen peroxide and peroxynitrite formed in mitochondria. Mitochondrial disfunction can lead to membrane lipoperoxidation, resulting in the formation of lipid-bound fatty acid hydroperoxides (&lt;sub>L&lt;/sub>FA-OOHs) which can be released to become free fatty acid hydroperoxides (&lt;sub>f&lt;/sub>FA-OOHs). Herein, we report that &lt;i>Hs&lt;/i>Prx3 is oxidized and hyperoxidized by &lt;sub>f&lt;/sub>FA-OOHs including those derived from arachidonic acid and eicosapentaenoic acid peroxidation at position 15 with remarkably high rate constants of oxidation (>3.5 × 10&lt;sup>7&lt;/sup> M&lt;sup>-1&lt;/sup>s&lt;sup>-1&lt;/sup>) and hyperoxidation (~2 × 10&lt;sup>7&lt;/sup> M&lt;sup>-1&lt;/sup>s&lt;sup>-1&lt;/sup>). The endoperoxide-hydroperoxide P</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Feb</publication><modification>2026-04-08T12:50:12.432Z</modification><creation>2024-11-20T00:47:00.241Z</creation></dates><accession>S-EPMC9952270</accession><cross_references><pubmed>36829967</pubmed><doi>10.3390/antiox12020408</doi></cross_references></HashMap>