A Naturally Occurring Inhibitor of Mitochondrial Adenosine Triphosphatase, J Biol Chem, vol.238, p.14109217, 1963. ,
The IF(1) inhibitor protein of the mitochondrial F(1)F(0)-ATPase, Biochim Biophys Acta, vol.1458, issue.2-3, p.10838049, 2000. ,
Assembling the mitochondrial ATP synthase, Proc Natl Acad Sci U S A, vol.115, issue.12, p.5866614, 2018. ,
Mitochondrial diseases. Nat Rev Dis Primers, vol.2, p.16080, 2016. ,
, Diseases of Mitochondrial Genetic Origin. Front Physiol, vol.9, p.5893901, 2018.
Respiratory chain complex V deficiency due to a mutation in the assembly gene ATP12, J Med Genet, vol.41, issue.2, p.14757859, 2004. ,
TMEM70 mutations cause isolated ATP synthase deficiency and neonatal mitochondrial encephalocardiomyopathy, Nat Genet, vol.40, issue.11, p.18953340, 2008. ,
Mitochondrial ATP synthase deficiency due to a mutation in the ATP5E gene for the F1 epsilon subunit, Hum Mol Genet, vol.19, issue.17, pp.3430-3439, 2010. ,
A complex V ATP5A1 defect causes fatal neonatal mitochondrial encephalopathy, Brain, vol.136, pp.1544-54, 2013. ,
Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder, Am J Hum Genet, vol.102, issue.3, p.6117612, 2018. ,
USMG5 Ashkenazi Jewish founder mutation impairs mitochondrial complex V dimerization and ATP synthesis, Hum Mol Genet, vol.27, issue.19, p.6140788, 2018. ,
OXA1L mutations cause mitochondrial encephalopathy and a combined oxidative phosphorylation defect, EMBO Mol Med, vol.10, issue.11, p.6220311, 2018. ,
Estimation of the turnover number of bovine heart F0F1 complexes for ATP synthesis, Biochemistry, vol.27, issue.1, pp.335-375, 1988. ,
Cellular and functional analysis of four mutations located in the mitochondrial ATPase6 gene, J Cell Biochem, vol.106, issue.5, pp.878-86, 2009. ,
Consequences of the pathogenic T9176C mutation of human mitochondrial DNA on yeast mitochondrial ATP synthase ,
URL : https://hal.archives-ouvertes.fr/hal-00450957
, Biochim Biophys Acta, vol.1797, issue.6-7, pp.1105-1117, 2010.
Preparation and properties of DPNH-coenzyme Q reductase (complex I of the respiratory chain). In: Estabrook RW, Methods in Enzymology, vol.10, pp.235-244, 1967. ,
How the N-terminal extremity of Saccharomyces cerevisiae IF1 interacts with ATP synthase: a kinetic approach, Biochim Biophys Acta, vol.1807, issue.2, p.20951672, 2011. ,
In: Estabrook RW, Pullman ME, editors. Oxidation and Phosphorylation. Methods in Enzymology, vol.10, pp.231-236, 1967. ,
Blue native PAGE, Nat Protoc, vol.1, issue.1, p.17406264, 2006. ,
Slow binding of ATP to noncatalytic nucleotide binding sites which accelerates catalysis is responsible for apparent negative cooperativity exhibited by the bovine mitochondrial F1-ATPase, J Biol Chem, vol.268, issue.3, p.8420930, 1993. ,
Development and implementation of standardized respiratory chain spectrophotometric assays for clinical diagnosis. Mitochondrion, vol.9, pp.331-340, 2009. ,
URL : https://hal.archives-ouvertes.fr/inserm-00516056
The molecular basis for tissue specificity of the oxidative phosphorylation deficiencies in patients with mutations in the mitochondrial translation factor EFG1, Hum Mol Genet, vol.15, issue.11, pp.1835-1881, 2006. ,
The ectopic F(O)F(1) ATP synthase of rat liver is modulated in acute cholestasis by the inhibitor protein IF1, J Bioenerg Biomembr, vol.42, issue.2, pp.117-140, 2010. ,
Evaluation of basic mitochondrial functions using rat tissue homogenates, Mitochondrion, vol.11, issue.5, p.21664301, 2011. ,
Episodic weakness due to mitochondrial DNA MT-ATP6/8 mutations, Neurology, vol.81, issue.21, p.24153443, 2013. ,
Adult-onset spinocerebellar ataxia syndromes due to MTATP6 mutations, J Neurol Neurosurg Psychiatry, vol.83, issue.9, p.22577227, 2012. ,
Identification of ataxia-associated mtDNA mutations (m.4052T>C and m.9035T>C) and evaluation of their pathogenicity in transmitochondrial cybrids, Muscle Nerve, vol.40, issue.3, pp.381-94, 2009. ,
Biochemical and molecular investigations in respiratory chain deficiencies, Clin Chim Acta, vol.228, issue.1, pp.35-51, 1994. ,
Reduced respiratory control with ADP and changed pattern of respiratory chain enzymes as a result of selective deficiency of the mitochondrial ATP synthase, Pediatr Res, vol.55, issue.6, p.15155867, 2004. ,
Three spectrophotometric assays for the measurement of the five respiratory chain complexes in minute biological samples, Clin Chim Acta, vol.374, p.16828729, 2006. ,
Investigation of the role and mechanism of IF1 and STF1 proteins, twin inhibitory peptides which interact with the yeast mitochondrial ATP synthase, Biochemistry, vol.42, issue.24, pp.7626-7662, 2003. ,
Homologous and heterologous inhibitory effects of ATPase inhibitor proteins on F-ATPases, J Biol Chem, vol.277, issue.44, pp.41334-41375, 2002. ,
Unsolved issues related to human mitochondrial diseases, Biochimie, vol.100, pp.171-177, 2014. ,
URL : https://hal.archives-ouvertes.fr/inserm-00877429
Identification of tyrosine-phosphorylated proteins of the mitochondrial oxidative phosphorylation machinery, Cell Mol Life Sci, vol.62, issue.13, p.15924266, 2005. ,
Threshold effect and tissue specificity. Implication for mitochondrial cytopathies, J Biol Chem, vol.274, issue.47, p.10559224, 1999. ,
Ecto-F(1)-ATPase: a moonlighting protein complex and an unexpected apoA-I receptor, World J Gastroenterol, vol.16, issue.47, p.3007107, 2010. ,
Isolation of mitochondria by gentle cell membrane disruption, and their subsequent characterization, Biochem Biophys Res Commun, vol.463, issue.4, pp.563-571, 2015. ,
Efficient isolation of pure and functional mitochondria from mouse tissues using automated tissue disruption and enrichment with anti-TOM22 magnetic beads, PLoS One, vol.8, issue.12, p.3861405, 2013. ,
A semi-automated method for isolating functionally intact mitochondria from cultured cells and tissue biopsies, Anal Biochem, vol.443, issue.1, pp.66-74, 2013. ,
The ATPase inhibitor protein from bovine heart mitochondria: the minimal inhibitory sequence, Biochemistry, vol.35, issue.49, pp.15618-15643, 1996. ,