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细胞质和核铁硫蛋白的成熟。

Maturation of cytosolic and nuclear iron-sulfur proteins.

机构信息

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.

出版信息

Trends Cell Biol. 2014 May;24(5):303-12. doi: 10.1016/j.tcb.2013.11.005. Epub 2013 Dec 3.

Abstract

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.

摘要

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。

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