Py Béatrice, Barras Frédéric
Laboratoire de Chimie Bactérienne, UMR 7283 CNRS-Aix-Marseille Université, Institut de Microbiologie de la Méditerranée, 31, chemin Joseph Aiguier, 13009 Marseille, France.
Med Sci (Paris). 2014 Dec;30(12):1110-22. doi: 10.1051/medsci/20143012014. Epub 2014 Dec 24.
Iron-sulfur clusters (Fe-S) are ubiquitous cofactors present in numerous proteins of most living organisms. By way of an example, the E. coli bacterium synthesizes more that 130 different types of Fe-S proteins. Fe-S proteins are involved in a great diversity of biological processes, ranging from respiration, photosynthesis, central metabolism, to genetic expression and genomic stability. Proteins can acquire spontaneously Fe-S clusters in vitro, but in vivo, dedicated molecular machineries are necessary. Dysfunction of these machineries alters cellular capacities leading to lethality in bacteria and severe pathologies in humans. In this review we will describe how cells make Fe-S clusters and deliver them to clients proteins. The importance of Fe-S clusters homeostasis will be illustrated by reporting a list of cellular dysfunctions associated with mutations altering either Fe-S proteins or Fe-S biogenesis machineries.
铁硫簇(Fe-S)是大多数生物体众多蛋白质中普遍存在的辅因子。例如,大肠杆菌能合成130多种不同类型的铁硫蛋白。铁硫蛋白参与了多种多样的生物过程,从呼吸作用、光合作用、中心代谢到基因表达和基因组稳定性。蛋白质在体外可以自发获得铁硫簇,但在体内,则需要专门的分子机制。这些机制的功能障碍会改变细胞能力,导致细菌死亡和人类严重疾病。在这篇综述中,我们将描述细胞如何制造铁硫簇并将其传递给客户蛋白。通过列出与改变铁硫蛋白或铁硫生物合成机制的突变相关的一系列细胞功能障碍,将说明铁硫簇稳态的重要性。