共 43 条
Two-stage binding of mitochondrial ferredoxin-2 to the core iron-sulfur cluster assembly complex
被引:1
|作者:
Steinhilper, Ralf
[1
]
Boss, Linda
[2
,3
]
Freibert, Sven-A.
[2
,3
]
Schulz, Vinzent
[2
,3
]
Krapoth, Nils
[2
,3
]
Kaltwasser, Susann
[4
]
Lill, Roland
[2
,3
]
Murphy, Bonnie J.
[1
]
机构:
[1] Max Planck Inst Biophys, Redox & Metalloprotein Res Grp, Max von Laue Str 3, D-60438 Frankfurt, Germany
[2] Philipps Univ Marburg, Inst Zytobiol, Karl Von Frisch Str 14, D-35032 Marburg, Germany
[3] Zent Synthet Mikrobiol Synmikro, Karl Von Frisch Str 14, D-35032 Marburg, Germany
[4] Max Planck Inst Biophys, Cent Electron Microscopy Facil, Max Laue Str 3, D-60438 Frankfurt, Germany
关键词:
CYSTEINE DESULFURASE;
ELECTRON;
PROTEIN;
REDUCTASE;
FRATAXIN;
BIOSYNTHESIS;
BIOGENESIS;
FEATURES;
D O I:
10.1038/s41467-024-54585-4
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Iron-sulfur (FeS) protein biogenesis in eukaryotes begins with the de novo assembly of [2Fe-2S] clusters by the mitochondrial core iron-sulfur cluster assembly (ISC) complex. This complex comprises the scaffold protein ISCU2, the cysteine desulfurase subcomplex NFS1-ISD11-ACP1, the allosteric activator frataxin (FXN) and the electron donor ferredoxin-2 (FDX2). The structural interaction of FDX2 with the complex remains unclear. Here, we present cryo-EM structures of the human FDX2-bound core ISC complex showing that FDX2 and FXN compete for overlapping binding sites. FDX2 binds in either a 'distal' conformation, where its helix F interacts electrostatically with an arginine patch of NFS1, or a 'proximal' conformation, where this interaction tightens and the FDX2-specific C terminus binds to NFS1, facilitating the movement of the [2Fe-2S] cluster of FDX2 closer to the ISCU2 FeS cluster assembly site for rapid electron transfer. Structure-based mutational studies verify the contact areas of FDX2 within the core ISC complex.
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页数:14
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