Institut für Zytobiologie, Philipps-Universität Marburg, Robert-Koch-Strasse 6, 35032 Marburg, Germany.
Institut für Zytobiologie, Philipps-Universität Marburg, Robert-Koch-Strasse 6, 35032 Marburg, Germany; Max-Planck-Institut für Terrestrische Mikrobiologie, Karl-von-Frisch-Strasse 10, 35043 Marburg, Germany; LOEWE (Landes-Offensive zur Entwicklung Wissenschaftlich-Ökonomischer Exzellenz) Zentrum für Synthetische Mikrobiologie (SynMikro), Hans-Meerwein-Strasse, 35043 Marburg, Germany.
Trends Cell Biol. 2014 May;24(5):303-12. doi: 10.1016/j.tcb.2013.11.005. Epub 2013 Dec 3.
Eukaryotic cells contain numerous cytosolic and nuclear iron-sulfur (Fe/S) proteins that perform key functions in metabolic catalysis, iron regulation, protein translation, DNA synthesis, and DNA repair. Synthesis of Fe/S clusters and their insertion into apoproteins are essential for viability and are conserved in eukaryotes. The process is catalyzed in two major steps by the CIA (cytosolic iron-sulfur protein assembly) machinery encompassing nine known proteins. First, a [4Fe-4S] cluster is assembled on a scaffold complex. This step requires a sulfur-containing compound from mitochondria and reducing equivalents from an electron transfer chain. Second, the Fe/S cluster is transferred from the scaffold to specific apoproteins by the CIA targeting complex. This review summarizes our molecular knowledge on CIA protein function during the assembly process.
真核细胞含有许多胞质和核内铁硫 (Fe/S) 蛋白,这些蛋白在代谢催化、铁调节、蛋白质翻译、DNA 合成和 DNA 修复中发挥关键作用。Fe/S 簇的合成及其插入到脱辅基蛋白中对于生存能力是必不可少的,并且在真核生物中是保守的。该过程由 CIA(胞质铁硫蛋白组装)机制催化,该机制包含九个已知蛋白。首先,在支架复合物上组装一个 [4Fe-4S] 簇。这一步需要来自线粒体的含硫化合物和来自电子传递链的还原当量。其次,CIA 靶向复合物将 Fe/S 簇从支架转移到特定的脱辅基蛋白上。本综述总结了我们对 CIA 蛋白在组装过程中功能的分子认识。