The mitochondrial inhibitor IF1 binds to the ATP synthase OSCP subunit and protects cancer cells from apoptosis

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作者
Chiara Galber
Simone Fabbian
Cristina Gatto
Martina Grandi
Stefania Carissimi
Manuel Jesus Acosta
Gianluca Sgarbi
Natascia Tiso
Francesco Argenton
Giancarlo Solaini
Alessandra Baracca
Massimo Bellanda
Valentina Giorgio
机构
[1] University of Bologna,Department of Biomedical and Neuromotor Sciences
[2] Consiglio Nazionale delle Ricerche Institute of Neuroscience,Department of Chemical Science
[3] University of Padova,Department of Biology
[4] University of Padova,undefined
[5] Consiglio Nazionale delle Ricerche Institute of Biomolecular Chemistry,undefined
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Cell Death & Disease | / 14卷
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摘要
The mitochondrial protein IF1 binds to the catalytic domain of the ATP synthase and inhibits ATP hydrolysis in ischemic tissues. Moreover, IF1 is overexpressed in many tumors and has been shown to act as a pro-oncogenic protein, although its mechanism of action is still debated. Here, we show that ATP5IF1 gene disruption in HeLa cells decreases colony formation in soft agar and tumor mass development in xenografts, underlining the role of IF1 in cancer. Notably, the lack of IF1 does not affect proliferation or oligomycin-sensitive mitochondrial respiration, but it sensitizes the cells to the opening of the permeability transition pore (PTP). Immunoprecipitation and proximity ligation analysis show that IF1 binds to the ATP synthase OSCP subunit in HeLa cells under oxidative phosphorylation conditions. The IF1–OSCP interaction is confirmed by NMR spectroscopy analysis of the recombinant soluble proteins. Overall, our results suggest that the IF1-OSCP interaction protects cancer cells from PTP-dependent apoptosis under normoxic conditions.
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[1]  
Solaini G(2005)Biochemical dysfunction in heart mitochondria exposed to ischaemia and reperfusion Biochem J 390 377-94
[2]  
Harris DA(2009)IF1: setting the pace of the F1Fo-ATP synthase Trends Biochem Sci 34 343-50
[3]  
Campanella M(1987)Protonic inhibition o f the mitochondrial adenosine 5’-triphosphatase in ischemic cardiac muscle. Reversible binding of the ATP ase inhibitor protein to the mitochondrial ATPase during ischemia J Mol Cell Cardiol 19 661-8
[4]  
Parker N(2007)How the regulatory protein, IF1, inhibits F1-ATPase from bovine mitochondria Proc Natl Acad Sci 104 15671-6
[5]  
Tan CH(2014)Pathway of binding of the intrinsically disordered mitochondrial inhibitor protein to F1-ATPase Proc Natl Acad Sci USA 111 11305-10
[6]  
Hall AM(2021)Kinetic analysis of the inhibition mechanism of bovine mitochondrial F1-ATPase inhibitory protein using biochemical assay J Biochem 170 79-87
[7]  
Duchen MR(2003)The structure of bovine F1-ATPase in complex with its regulatory protein IF1 Nat Struct Biol 10 744-50
[8]  
Rouslin W(2011)Binding of the inhibitor protein IF1 to bovine F1-ATPase J Mol Biol 406 443-53
[9]  
Pullman ME(2019)Extrinsic conditions influence the self-association and structure of IF 1, the regulatory protein of mitochondrial ATP synthase Proc Natl Acad Sci 116 10354-59.
[10]  
Gledhill JR(2019)Cryo-EM structure of the mammalian ATP synthase tetramer bound with inhibitory protein IF1 Science 364 1068-75