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   <dc:title>Physiologically relevant reconstitution of iron-sulfur cluster biosynthesis uncovers persulfide- processing functions of ferredoxin-2 and frataxin</dc:title>
   <dc:creator>Gervason, Sylvain</dc:creator>
   <dc:creator>Larkem, Djabir</dc:creator>
   <dc:creator>Mansour, Amir Ben</dc:creator>
   <dc:creator>Botzanowski, Thomas</dc:creator>
   <dc:creator>Müller, Christina S.</dc:creator>
   <dc:creator>Pecqueur, Ludovic</dc:creator>
   <dc:creator>Le Pavec, Gwenaelle</dc:creator>
   <dc:creator>Delaunay-Moisan, Agnès</dc:creator>
   <dc:creator>Brun Cubero, Omar</dc:creator>
   <dc:creator>Agramunt, Jordi</dc:creator>
   <dc:creator>Grandas Sagarra, Anna</dc:creator>
   <dc:creator>Fontecave, Marc</dc:creator>
   <dc:creator>Schünemann, Volker</dc:creator>
   <dc:creator>Cianférani, Sarah</dc:creator>
   <dc:creator>Sizun, Christina</dc:creator>
   <dc:creator>Toledano, Michel B.</dc:creator>
   <dc:creator>D'Autréaux, Benoit</dc:creator>
   <dc:subject>Malalties neurodegeneratives</dc:subject>
   <dc:subject>Bioquímica</dc:subject>
   <dc:subject>Biosíntesi</dc:subject>
   <dc:subject>Proteïnes</dc:subject>
   <dc:subject>Neurodegenerative Diseases</dc:subject>
   <dc:subject>Biochemistry</dc:subject>
   <dc:subject>Biosynthesis</dc:subject>
   <dc:subject>Proteins</dc:subject>
   <dc:description>Iron-sulfur (Fe-S) clusters are essential protein cofactors whose biosynthetic defects lead to severe diseases among which is Friedreich's ataxia caused by impaired expression of frataxin (FXN). Fe-S clusters are biosynthesized on the scaffold protein ISCU, with cysteine desulfurase NFS1 providing sulfur as persulfide and ferredoxin FDX2 supplying electrons, in a process stimulated by FXN but not clearly understood. Here, we report the breakdown of this process, made possible by removing a zinc ion in ISCU that hinders iron insertion and promotes non-physiological Fe-S cluster synthesis from free sulfide in vitro. By binding zinc-free ISCU, iron drives persulfide uptake from NFS1 and allows persulfide reduction into sulfide by FDX2, thereby coordinating sulfide production with its availability to generate Fe-S clusters. FXN stimulates the whole process by accelerating persulfide transfer. We propose that this reconstitution recapitulates physiological conditions which provides a model for Fe-S cluster biosynthesis, clarifies the roles of FDX2 and FXN and may help develop Friedreich's ataxia therapies.</dc:description>
   <dc:date>2019-09-19T14:47:35Z</dc:date>
   <dc:date>2019-09-19T14:47:35Z</dc:date>
   <dc:date>2019</dc:date>
   <dc:date>2019-09-19T14:47:36Z</dc:date>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
   <dc:identifier>2041-1723</dc:identifier>
   <dc:identifier>https://hdl.handle.net/2445/140541</dc:identifier>
   <dc:identifier>691256</dc:identifier>
   <dc:identifier>31395877</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>Reproducció del document publicat a: https://doi.org/10.1038/s41467-019-11470-9</dc:relation>
   <dc:relation>Nature Communications, 2019, vol. 10, p. 3566</dc:relation>
   <dc:relation>https://doi.org/10.1038/s41467-019-11470-9</dc:relation>
   <dc:rights>cc-by (c) Gervason, Sylvain et al., 2019</dc:rights>
   <dc:rights>http://creativecommons.org/licenses/by/3.0/es</dc:rights>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:format>13 p.</dc:format>
   <dc:format>application/pdf</dc:format>
   <dc:publisher>Nature Publishing Group</dc:publisher>
   <dc:source>Articles publicats en revistes (Química Inorgànica i Orgànica)</dc:source>
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