在ISCU架构蛋白的组装部位插入铁是启动Fe-S集群生物合成的保存过程
Batoul Srour1, Sylvain Gervason1, Maren Hellen Hoock2
1Université Paris-Saclay, CEA, CNRS, Institute for Integrative Biology of the Cell (I2BC), 91198 Gif-sur-Yvette, France.
Journal of the American Chemical Society
|September 19, 2022
概括
铁-硫生物合成始于将铁插入ISCU支架蛋白
科学领域:
- 生物化学
- 分子生物学
- 结构生物学
背景情况:
- 铁硫 (Fe-S) 集群是蛋白质中的重要假体组.
- 它们的生物合成包括像ISCU这样的支架蛋白和保存机械.
- 铁在ISCU中的初始插入机制尚不清楚.
研究的目的:
- 阐明初始铁入ISCU支架蛋白质的机制.
- 在Fe-S集群生物合成过程中确定铁的结合部位和协调.
- 研究保存的氨基酸在ISCU铁结合和硫获取中的作用.
主要方法:
- 大小排除色谱 (SEC)
- 循环二极化 (CD) 光谱
- 莫斯巴尔光谱学
- 位点定向的突变发生
- 核磁共振 (NMR) 光谱学
- 射线吸收光谱学
- 电子磁共振 (EPR) 光谱
主要成果:
- 铁通过一个或两个囊 (1-Cys和2-Cys形式) 与ISCU组装部位结合.
- 在pH值为8.0时,2-Cys形式占主导地位,与Fe-S集成活性相关.
- 铁是由Cys35,Asp37,Cys61和His103在四面体几何中以2-Cys形式协调的.
- Cys104被定位为硫转移,特别是在His103缺席的时候.
结论:
- 启动Fe-S集群生物合成涉及将铁入ISCU组装现场.
- 通过ISCU建立了铁结合和协调的保护机制.
- 这些发现为Fe-S集群组装过程提供了结构性见解.
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