Interconversion between [2Fe-2S] and [4Fe-4S] cluster glutathione complexes

被引:9
|
作者
Invernici, Michele [1 ,2 ]
Selvolini, Giulia [3 ]
Silva, Jose Malanho [1 ,3 ]
Marrazza, Giovanna [3 ]
Ciofi-Baffoni, Simone [1 ,3 ]
Piccioli, Mario [1 ,2 ,3 ]
机构
[1] Univ Florence, Magnet Resonance Ctr CERM, Via L Sacconi 6, I-50019 Sesto Fiorentino, Italy
[2] Consorzio Interuniv Risonanze Magnet Metalloprot, Via L Sacconi 6, I-50019 Sesto Fiorentino, Italy
[3] Univ Florence, Dept Chem Ugo Schiff, Via Lastruccia 3, I-50019 Sesto Fiorentino, Italy
基金
欧盟地平线“2020”;
关键词
IRON-SULFUR; MITOCHONDRIAL ABCB7; METAL-COMPLEXES; MECHANISM; CYTOSOL; CELLS; PH;
D O I
10.1039/d1cc03566e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We present here how different iron-sulfide-glutathione ratios, applied in in vitro conditions comparable to those present in the mitochondrial matrix, affect the speciation of iron-sulfur cluster glutathione complexes. An excess of sulfide with respect to iron ions promotes the formation of a tetranuclear [(Fe2Fe2S4)-Fe-II-S-III(GS)(4)](2-) complex, while an excess of iron ions favors the formation of a dinuclear [(FeFeS2)-Fe-II-S-III(GS)(4)](3-) complex. These two complexes establish an interconversion equilibrium. The latter might play a role in the composition of the mitochondrial labile iron pool potentially contributing to the regulation of cellular iron homeostasis.
引用
收藏
页码:3533 / 3536
页数:4
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