<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Slavic K</submitter><funding>European Research Council</funding><pagination>10403</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4735874</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>7</volume><pubmed_abstract>Iron is an essential micronutrient but is also highly toxic. In yeast and plant cells, a key detoxifying mechanism involves iron sequestration into intracellular storage compartments, mediated by members of the vacuolar iron-transporter (VIT) family of proteins. Here we study the VIT homologue from the malaria parasites Plasmodium falciparum (PfVIT) and Plasmodium berghei (PbVIT). PfVIT-mediated iron transport in a yeast heterologous expression system is saturable (Km ∼ 14.7 μM), and selective for Fe(2+) over other divalent cations. PbVIT-deficient P. berghei lines (Pbvit(-)) show a reduction in parasite load in both liver and blood stages of infection in mice. Moreover, Pbvit(-) parasites have higher levels of labile iron in blood stages and are more sensitive to increased iron levels in </pubmed_abstract><journal>Nature communications</journal><pubmed_title>A vacuolar iron-transporter homologue acts as a detoxifier in Plasmodium.</pubmed_title><pmcid>PMC4735874</pmcid><funding_grant_id>311502</funding_grant_id><pubmed_authors>Vera I</pubmed_authors><pubmed_authors>Lahree A</pubmed_authors><pubmed_authors>Bouyer G</pubmed_authors><pubmed_authors>Krishna S</pubmed_authors><pubmed_authors>Hanson KK</pubmed_authors><pubmed_authors>Pittman JK</pubmed_authors><pubmed_authors>Staines HM</pubmed_authors><pubmed_authors>Mota MM</pubmed_authors><pubmed_authors>Slavic K</pubmed_authors></additional><is_claimable>false</is_claimable><name>A vacuolar iron-transporter homologue acts as a detoxifier in Plasmodium.</name><description>Iron is an essential micronutrient but is also highly toxic. In yeast and plant cells, a key detoxifying mechanism involves iron sequestration into intracellular storage compartments, mediated by members of the vacuolar iron-transporter (VIT) family of proteins. Here we study the VIT homologue from the malaria parasites Plasmodium falciparum (PfVIT) and Plasmodium berghei (PbVIT). PfVIT-mediated iron transport in a yeast heterologous expression system is saturable (Km ∼ 14.7 μM), and selective for Fe(2+) over other divalent cations. PbVIT-deficient P. berghei lines (Pbvit(-)) show a reduction in parasite load in both liver and blood stages of infection in mice. Moreover, Pbvit(-) parasites have higher levels of labile iron in blood stages and are more sensitive to increased iron levels in </description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Jan</publication><modification>2025-04-22T19:56:50.197Z</modification><creation>2019-03-27T02:08:02Z</creation></dates><accession>S-EPMC4735874</accession><cross_references><pubmed>26786069</pubmed><doi>10.1038/ncomms10403</doi></cross_references></HashMap>