<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Turnsek J</submitter><funding>NIEHS NIH HHS</funding><funding>Biological and Environmental Research</funding><funding>Gordon and Betty Moore Foundation</funding><funding>National Institutes of Health</funding><funding>Czech Science Foundation</funding><funding>NIH HHS</funding><funding>NIGMS NIH HHS</funding><funding>National Science Foundation</funding><funding>European Regional Development Fund</funding><pagination>e52770</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7972479</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>10</volume><pubmed_abstract>Iron is a biochemically critical metal cofactor in enzymes involved in photosynthesis, cellular respiration, nitrate assimilation, nitrogen fixation, and reactive oxygen species defense. Marine microeukaryotes have evolved a phytotransferrin-based iron uptake system to cope with iron scarcity, a major factor limiting primary productivity in the global ocean. Diatom phytotransferrin is endocytosed; however, proteins downstream of this environmentally ubiquitous iron receptor are unknown. We applied engineered ascorbate peroxidase APEX2-based subcellular proteomics to catalog proximal proteins of phytotransferrin in the model marine diatom &lt;i>Phaeodactylum tricornutum&lt;/i>. Proteins encoded by poorly characterized iron-sensitive genes were identified including three that are expressed from a </pubmed_abstract><journal>eLife</journal><pubmed_title>Proximity proteomics in a marine diatom reveals a putative cell surface-to-chloroplast iron trafficking pathway.</pubmed_title><pmcid>PMC7972479</pmcid><funding_grant_id>GBMF5006</funding_grant_id><funding_grant_id>F31 1F31ES030613-01</funding_grant_id><funding_grant_id>NSF-OCE-1756884</funding_grant_id><funding_grant_id>NSF-MCB-1818390</funding_grant_id><funding_grant_id>F31 ES030613</funding_grant_id><funding_grant_id>GBMF3828</funding_grant_id><funding_grant_id>CZ.02.1.01/0.0/0.0/16_019/0000759</funding_grant_id><funding_grant_id>GBMF4958</funding_grant_id><funding_grant_id>DE-SC0018344</funding_grant_id><funding_grant_id>R24 GM137200</funding_grant_id><funding_grant_id>1F31ES030613-01</funding_grant_id><funding_grant_id>21-03224S</funding_grant_id><pubmed_authors>Allen AE</pubmed_authors><pubmed_authors>Bielinski VA</pubmed_authors><pubmed_authors>Brunson JK</pubmed_authors><pubmed_authors>Viedma MDPM</pubmed_authors><pubmed_authors>Horak A</pubmed_authors><pubmed_authors>Obornik M</pubmed_authors><pubmed_authors>Turnsek J</pubmed_authors><pubmed_authors>Deerinck TJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Proximity proteomics in a marine diatom reveals a putative cell surface-to-chloroplast iron trafficking pathway.</name><description>Iron is a biochemically critical metal cofactor in enzymes involved in photosynthesis, cellular respiration, nitrate assimilation, nitrogen fixation, and reactive oxygen species defense. Marine microeukaryotes have evolved a phytotransferrin-based iron uptake system to cope with iron scarcity, a major factor limiting primary productivity in the global ocean. Diatom phytotransferrin is endocytosed; however, proteins downstream of this environmentally ubiquitous iron receptor are unknown. We applied engineered ascorbate peroxidase APEX2-based subcellular proteomics to catalog proximal proteins of phytotransferrin in the model marine diatom &lt;i>Phaeodactylum tricornutum&lt;/i>. Proteins encoded by poorly characterized iron-sensitive genes were identified including three that are expressed from a </description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Feb</publication><modification>2026-04-13T03:12:40.562Z</modification><creation>2025-02-19T02:12:53.86Z</creation></dates><accession>S-EPMC7972479</accession><cross_references><pubmed>33591270</pubmed><doi>10.7554/eLife.52770</doi></cross_references></HashMap>