20 results on '"Sideris, Dionisia P."'
Search Results
2. The ubiquitin kinase PINK1 recruits autophagy receptors to induce mitophagy
- Author
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Lazarou, Michael, Sliter, Danielle A., Kane, Lesley A., Sarraf, Shireen A., Wang, Chunxin, Burman, Jonathon L., Sideris, Dionisia P., Fogel, Adam I., and Youle, Richard J.
- Subjects
Ubiquitin -- Research ,Membrane proteins -- Research ,Ligases -- Research ,Mitochondrial DNA -- Research ,Environmental issues ,Science and technology ,Zoology and wildlife conservation - Abstract
Protein aggregates and damaged organelles are tagged with ubiquitin chains to trigger selective autophagy. To initiate mitophagy, the ubiquitin kinase PINK1 phosphorylates ubiquitin to activate the ubiquitin ligase parkin, which builds ubiquitin chains on mitochondrial outer membrane proteins, where they act to recruit autophagy receptors. Using genome editing to knockout five autophagy receptors in HeLa cells, here we show that two receptors previously linked to xenophagy, NDP52 and optineurin, are the primary receptors for PINK1- and parkin-mediated mitophagy. PINK1 recruits NDP52 and optineurin, but not p62, to mitochondria to activate mitophagy directly, independently of parkin. Once recruited to mitochondria, NDP52 and optineurin recruit the autophagy factors ULK1, DFCP1 and WIPI1 to focal spots proximal to mitochondria, revealing a function for these autophagy receptors upstream of LC3. This supports a new model in which PINK1-generated phospho-ubiquitin serves as the autophagy signal on mitochondria, and parkin then acts to amplify this signal. This work also suggests direct and broader roles for ubiquitin phosphorylation in other autophagy pathways., Selective autophagy clears intracellular pathogens and mediates cellular quality control by engulfing cargo into autophagosomes and delivering it to lysosomes for degradation. Autophagy receptors bind ubiquitinated cargo and LC3-coated phagophores [...]
- Published
- 2015
- Full Text
- View/download PDF
3. A novel intermembrane space--targeting signal docks cysteines onto Mia40 during mitochondrial oxidative folding
- Author
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Sideris, Dionisia P., Petrakis, Nikos, Katrakili, Nitsa, Mikropoulou, Despina, Gallo, Angelo, Ciofi-Baffoni, Simone, Banci, Lucia, Bertini, Ivano, and Tokatlidis, Kostas
- Subjects
Cysteine -- Physiological aspects ,Cysteine -- Research ,Mitochondrial membranes -- Physiological aspects ,Mitochondrial membranes -- Research ,Oxidative stress -- Physiological aspects ,Oxidative stress -- Research ,Biological sciences - Abstract
Mia40 imports Cys-containing proteins into the mitochondrial intermembrane space (IMS) by ensuring their Cys-dependent oxidative folding. In this study, we show that the specific Cys of the substrate involved in docking with Mia40 is substrate dependent, the process being guided by an IMS-targeting signal (ITS) present in Mia40 substrates. The ITS is a 9-aa internal peptide that (a) is upstream or downstream of the docking Cys, (b) is sufficient for crossing the outer membrane and for targeting nonmitochondrial proteins, (c) forms an amphipathic helix with crucial hydrophobic residues on the side of the docking Cys and dispensable charged residues on the other side, and (d) fits complementary to the substrate cleft of Mia40 via hydrophobic interactions of micromolar affinity. We rationalize the dual function of Mia40 as a receptor and an oxidase in a two step--specific mechanism: an ITS-guided sliding step orients the substrate noncovalently, followed by docking of the substrate Cys now juxtaposed to pair with the Mia40 active Cys. doi/10.1083/jcb.200905134
- Published
- 2009
4. Translocation of mitochondrial inner-membrane proteins: conformation matters
- Author
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De Marcos-Lousa, Carine, Sideris, Dionisia P., and Tokatlidis, Kostas
- Subjects
Membrane proteins ,Biological sciences ,Chemistry - Abstract
To link to full-text access for this article, visit this link: http://dx.doi.org/10.1016/j.tibs.2006.03.006 Byline: Carine de Marcos-Lousa (a), Dionisia P Sideris (a)(b), Kostas Tokatlidis (a)(c) Abstract: Most of the mitochondrial inner-membrane proteins are generated without a presequence and their targeting depends on inadequately defined internal segments. Despite the numerous components of the import machinery identified by proteomics, the properties of hydrophobic import substrates remain poorly understood. Recent studies support several principles for these membrane proteins: first, they become organized into partially assembled forms within the translocon; second, they present noncontiguous targeting signals; and third, they induce conformational changes in translocase subunits, thereby mediating 'assembly on demand' of the import machinery. It is possible that the energy needed for these proteins to pass across the outer membrane, to travel through the intermembrane space and to target the inner-membrane surface is provided by conformational changes involving import components that seem to have natively unfolded structures. Such structural malleability might render some of the translocase subunits more adept at driving the protein import process. Author Affiliation: (a) Institute of Molecular Biology and Biotechnology, Foundation for Research and Technology (IMBB-FORTH), PO Box 1385, Heraklion 71110, Crete, Greece (b) Department of Biology, University of Crete, PO Box 2208, Heraklion 71409, Crete, Greece (c) Department of Chemistry, University of Crete, PO Box 1470, Heraklion 71409, Crete, Greece
- Published
- 2006
5. Biogenesis of yeast Mia40 – uncoupling folding from import and atypical recognition features
- Author
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Chatzi, Afroditi, Sideris, Dionisia P., Katrakili, Nitsa, Pozidis, Charalampos, and Tokatlidis, Kostas
- Published
- 2013
- Full Text
- View/download PDF
6. Oxidative folding of small Tims is mediated by site-specific docking onto Mia40 in the mitochondrial intermembrane space
- Author
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Sideris, Dionisia P. and Tokatlidis, Kostas
- Published
- 2007
7. Role of Membrane Association and Atg14-Dependent Phosphorylation in Beclin-1-Mediated Autophagy.
- Author
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Fogel, Adam I., Dlouhy, Brian J., Chunxin Wang, Seung-Wook Ryu, Neutzner, Albert, Hasson, Samuel A., Sideris, Dionisia P., Abeliovich, Hagai, and Youle, Richard J.
- Subjects
LYSOSOMES ,AUTOPHAGY ,ORGANELLES ,MOLECULAR biology ,CYTOLOGY - Abstract
During autophagy, a double membrane envelops cellular material for trafficking to the lysosome. Human beclin-1 and its yeast homologue, Atg6/Vps30, are scaffold proteins bound in a lipid kinase complex with multiple cellular functions, including autophagy. Several different Atg6 complexes exist, with an autophagy-specific form containing Atg14. However, the roles of Atg14 and beclin-1 in the activation of this complex remain unclear. We here addressed the mechanism of beclin-1 complex activation and reveal two critical steps in this pathway. First, we identified a unique domain in beclin-1, conserved in the yeast homologue Atg6, which is involved in membrane association and, unexpectedly, controls autophagosome size and number in yeast. Second, we demonstrated that human Atg14 is critical in controlling an autophagy-dependent phosphorylation of beclin-1. We map these novel phosphorylation sites to serines 90 and 93 and demonstrate that phosphorylation at these sites is necessary for maximal autophagy. These results help clarify the mechanism of beclin-1 and Atg14 during autophagy. [ABSTRACT FROM AUTHOR]
- Published
- 2013
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8. Balanced Ero1 activation and inactivation establishes ER redox homeostasis.
- Author
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Sunghwan Kim, Sideris, Dionisia P., Sevier, Carolyn S., and Kaiser, Chris A.
- Subjects
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ENDOPLASMIC reticulum , *PROTEIN folding , *GLUTATHIONE , *OXIDATION , *DISULFIDES - Abstract
The endoplasmic reticulum (ER) provides an environment optimized for oxidative protein folding through the action of Ero1p, which generates disulfide bonds, and Pdi1p, which receives disulfide bonds from Ero1p and transfers them to substrate proteins. Feedback regulation of Ero1p through reduction and oxidation of regulatory bonds within Ero1p is essential for maintaining the proper redox balance in the ER. In this paper, we show that Pdi1p is the key regulator of Ero1p activity. Reduced Pdi1p resulted in the activation of Ero1p by direct reduction of Ero1p regulatory bonds. Conversely, upon depletion of thiol substrates and accumulation of oxidized Pdi1p, Ero1p was inactivated by both autonomous oxidation and Pdi1pmediated oxidation of Ero1p regulatory bonds. Pdi1p responded to the availability of free thiols and the relative levels of reduced and oxidized glutathione in the ER to control Ero1p activity and ensure that cells generate the minimum number of disulfide bonds needed for efficient oxidative protein folding. [ABSTRACT FROM AUTHOR]
- Published
- 2012
- Full Text
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9. MIA40 is an oxidoreductase that catalyzes oxidative protein folding in mitochondria.
- Author
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Banci, Lucia, Bertini, Ivano, Cefaro, Chiara, Ciofi-Baffoni, Simone, Gallo, Angelo, Martinelli, Manuele, Sideris, Dionisia P, Katrakili, Nitsa, and Tokatlidis, Kostas
- Subjects
OXIDOREDUCTASES ,CATALYSIS ,OXIDATIVE stress ,PROTEIN folding ,MITOCHONDRIA ,SUBSTRATES (Materials science) ,THIOREDOXIN ,OXIDATION-reduction reaction - Abstract
MIA40 has a key role in oxidative protein folding in the mitochondrial intermembrane space. We present the solution structure of human MIA40 and its mechanism as a catalyst of oxidative folding. MIA40 has a 66-residue folded domain made of an α-helical hairpin core stabilized by two structural disulfides and a rigid N-terminal lid, with a characteristic CPC motif that can donate its disulfide bond to substrates. The CPC active site is solvent-accessible and sits adjacent to a hydrophobic cleft. Its second cysteine (Cys55) is essential in vivo and is crucial for mixed disulfide formation with the substrate. The hydrophobic cleft functions as a substrate binding domain, and mutations of this domain are lethal in vivo and abrogate binding in vitro. MIA40 represents a thioredoxin-unrelated, minimal oxidoreductase, with a facile CPC redox active site that ensures its catalytic function in oxidative folding in mitochondria. [ABSTRACT FROM AUTHOR]
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- 2009
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10. ICPBCZin: A red emitting ratiometric fluorescent indicator with nanomolar affinity for Zn2+ ions.
- Author
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Roussakis, Emmanuel, Voutsadaki, Styliani, Pinakoulaki, Eftychia, Sideris, Dionisia P., Tokatlidis, Kostas, and Katerinopoulos, Haralambos E.
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FLUORESCENCE spectroscopy ,ZINC compounds ,BENZIMIDAZOLES ,FLUORIMETRY ,WAVELENGTHS ,CHARGE exchange - Abstract
Summary: A new fluorescent Zn
2+ indicator, namely, ICPBCZin was synthesized and the spectral profile of its free and Zn2+ bound forms was studied. The newly synthesized zinc indicator incorporates as chromophore the chromeno [3′,2′:3,4]pyrido[1,2a] [1,3]benzimidazole moiety and belongs to the dicarboxylate-type of zinc probes. The compound is excited with visible light, exhibits high selectivity for zinc in the presence of calcium and other common biological ions, and its Zn2+ dissociation constant is 4.0nM. Fluorescence spectra studies of ICPBCZin indicated a clear shift in its emission wavelength maxima upon Zn2+ binding, as it belongs to the class of Photoinduced Charge Transfer (PCT) indicators, along with changes in fluorescence intensity that enable the compound to be used as a ratiometric, visible-excitable Zn2+ probe. [Copyright &y& Elsevier]- Published
- 2008
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11. Intimate Relations—Mitochondria and Ageing.
- Author
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Webb, Michael and Sideris, Dionisia P.
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MITOCHONDRIA , *GENETIC regulation , *BIOLOGY - Abstract
Mitochondrial dysfunction is associated with ageing, but the detailed causal relationship between the two is still unclear. We review the major phenomenological manifestations of mitochondrial age-related dysfunction including biochemical, regulatory and energetic features. We conclude that the complexity of these processes and their inter-relationships are still not fully understood and at this point it seems unlikely that a single linear cause and effect relationship between any specific aspect of mitochondrial biology and ageing can be established in either direction. [ABSTRACT FROM AUTHOR]
- Published
- 2020
- Full Text
- View/download PDF
12. PINK1/Parkin Influences Cell Cycle by Sequestering TBK1 at Damaged Mitochondria, Inhibiting Mitosis.
- Author
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Sarraf, Shireen A., Sideris, Dionisia P., Giagtzoglou, Nikolaos, Ni, Lina, Kankel, Mark W., Sen, Anindya, Bochicchio, Lauren E., Huang, Chiu-Hui, Nussenzweig, Samuel C., Worley, Stuart H., Morton, Paul D., Artavanis-Tsakonas, Spyros, Youle, Richard J., and Pickrell, Alicia M.
- Abstract
PINK1 and Parkin are established mediators of mitophagy, the selective removal of damaged mitochondria by autophagy. PINK1 and Parkin have been proposed to act as tumor suppressors, as loss-of-function mutations are correlated with enhanced tumorigenesis. However, it is unclear how PINK1 and Parkin act in coordination during mitophagy to influence the cell cycle. Here we show that PINK1 and Parkin genetically interact with proteins involved in cell cycle regulation, and loss of PINK1 and Parkin accelerates cell growth. PINK1- and Parkin-mediated activation of TBK1 at the mitochondria during mitophagy leads to a block in mitosis due to the sequestration of TBK1 from its physiological role at centrosomes during mitosis. Our study supports a diverse role for the far-reaching, regulatory effects of mitochondrial quality control in cellular homeostasis and demonstrates that the PINK1/Parkin pathway genetically interacts with the cell cycle, providing a framework for understanding the molecular basis linking PINK1 and Parkin to mitosis. • PINK1 and Parkin genetically interact with cell cycle-regulatory proteins • PINK1 and Parkin do not directly signal with the nuclear DNA damage response • Active TBK1 sequestered at damaged mitochondria during mitophagy perturbs mitosis • Fly ortholog of TBK1 rescues PINK1- and Parkin-knockout phenotypes Sarraf et al. use mouse and fly genetics to discover that PINK1 and Parkin influence cell cycle progression. Mitophagy and mitosis independently activate TBK1 at damaged mitochondria and centrosomes, respectively, influencing whether the cell will address mitochondrial quality control or progress with proliferation. [ABSTRACT FROM AUTHOR]
- Published
- 2019
- Full Text
- View/download PDF
13. Erratum to “ICPBCZin: A red emitting ratiometric fluorescent indicator with nanomolar affinity for Zn2+ ions” [Cell Calcium 44 (3) (2008) 270–275].
- Author
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Roussakis, Emmanuel, Voutsadaki, Styliani, Pinakoulaki, Eftychia, Sideris, Dionisia P., Tokatlidis, Kostas, and Katerinopoulos, Haralambos E.
- Published
- 2009
- Full Text
- View/download PDF
14. Erv1 Mediates the Mia40-dependent Protein Import Pathway and Provides a Functional Link to the Respiratory Chain by Shuttling Electrons to Cytochrome c
- Author
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Allen, Scott, Balabanidou, Vassilia, Sideris, Dionisia P., Lisowsky, Thomas, and Tokatlidis, Kostas
- Subjects
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PROTEINS , *PROTOPLASM , *MITOCHONDRIA , *MEMBRANE proteins - Abstract
Unlike matrix-targeted or inner membrane proteins, those that are targeted to the mitochondrial intermembrane space (IMS) do not require ATP or the inner membrane electrochemical potential. Their import is mediated primarily by the essential IMS protein Mia40/Tim40. Here, we show that the mitochondrial flavin adenine dinucleotide (FAD)-linked sulfhydryl oxidase Erv1 (essential for respiration and vegetative growth 1) plays a central role in the biogenesis of small, cysteine proteins of the IMS that are import substrates for Mia40. In a temperature-sensitive strain of Erv1, steady-state levels of small translocases of the inner membrane (Tims) are specifically affected when cells are grown at the non-permissive temperature. Furthermore, mitochondria isolated from the erv1-ts show a specific import and assembly defect for the small Tims but not in any other protein import pathway. Erv1 does not directly oxidise the small Tims, as thiol trapping assays show that the small Tims can still be oxidised in erv1-ts cells grown at the non-permissive temperature and in isolated mitochondria from this strain. Moreover, addition of pure Erv1 into erv1-ts mitochondria lacking the endogenous protein restores import and assembly of the small Tims only to an extent, arguing for a cascade of interactions with Erv1 rather than for a direct interaction of Erv1 with the small Tims. Cytochrome c (cyt c) is the in vivo oxidase for Erv1, as yeast cells mutated in cyt c cannot grow under anaerobic conditions. Therefore, Erv1 functionally links the Mia40-dependent import pathway to the Mia40-independent cyt c import pathway transferring electrons from the incoming precursors to cyt c as an acceptor. In this context, the protein import process is linked to the respiratory chain via the communication of Erv1 with cyt c. [Copyright &y& Elsevier]
- Published
- 2005
- Full Text
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15. Reciprocal Roles of Tom7 and OMA1 during Mitochondrial Import and Activation of PINK1.
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Sekine, Shiori, Wang, Chunxin, Sideris, Dionisia P., Bunker, Eric, Zhang, Zhe, and Youle, Richard J.
- Subjects
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PTEN protein , *GENETIC mutation , *C-terminal residues , *PATHOLOGICAL physiology , *PROTEASE inhibitors - Abstract
Summary Mutations in PTEN-induced kinase 1 (PINK1) can cause recessive early-onset Parkinson's disease (PD). Import arrest results in PINK1 kinase activation specifically on damaged mitochondria, triggering Parkin-mediated mitophagy. Here, we show that PINK1 import is less dependent on Tim23 than on mitochondrial membrane potential (ΔΨm). We identified a negatively charged amino acid cluster motif that is evolutionarily conserved just C-terminal to the PINK1 transmembrane. PINK1 that fails to accumulate at the outer mitochondrial membrane, either by mutagenesis of this negatively charged motif or by deletion of Tom7, is imported into depolarized mitochondria and cleaved by the OMA1 protease. Some PD patient mutations also are defective in import arrest and are rescued by the suppression of OMA1, providing a new potential druggable target for PD. These results suggest that ΔΨm loss-dependent PINK1 import arrest does not result solely from Tim23 inactivation but also through an actively regulated "tug of war" between Tom7 and OMA1. Graphical Abstract Highlights • Without Tom7, PINK1 is imported into depolarized mitochondria • Negatively charged motif in PINK1 is required for PINK1 import arrest • OMA1 degrades PINK1 that fails to accumulate on depolarized mitochondria • OMA1 deletion rescues Parkin recruitment for some PD-related PINK1 mutants PINK1 activation on damaged mitochondria triggering Parkin-mediated mitophagy is achieved by PINK1 import arrest within mitochondria. Sekine et al. show that this process involves competition between two mitochondrial proteins, Tom7 and OMA1, where a specific motif in PINK1 plays an important role, and describe its pathophysiologic relevance in Parkinson's disease. [ABSTRACT FROM AUTHOR]
- Published
- 2019
- Full Text
- View/download PDF
16. Endogenous Parkin Preserves Dopaminergic Substantia Nigral Neurons following Mitochondrial DNA Mutagenic Stress.
- Author
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Pickrell, Alicia M., Huang, Chiu-Hui, Kennedy, Scott R., Ordureau, Alban, Sideris, Dionisia P., Hoekstra, Jake G., Harper, J. Wade, and Youle, Richard J.
- Subjects
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PARKINSON'S disease diagnosis , *DOPAMINERGIC neurons , *SUBSTANTIA nigra , *MITOCHONDRIAL DNA , *PHYSIOLOGICAL stress , *UBIQUITIN ligases - Abstract
Summary Parkinson’s disease (PD) is a neurodegenerative disease caused by the loss of dopaminergic neurons in the substantia nigra. PARK2 mutations cause early-onset forms of PD. PARK2 encodes an E3 ubiquitin ligase, Parkin, that can selectively translocate to dysfunctional mitochondria to promote their removal by autophagy. However, Parkin knockout (KO) mice do not display signs of neurodegeneration. To assess Parkin function in vivo, we utilized a mouse model that accumulates dysfunctional mitochondria caused by an accelerated generation of mtDNA mutations (Mutator mice). In the absence of Parkin, dopaminergic neurons in Mutator mice degenerated causing an L-DOPA reversible motor deficit. Other neuronal populations were unaffected. Phosphorylated ubiquitin was increased in the brains of Mutator mice, indicating PINK1-Parkin activation. Parkin loss caused mitochondrial dysfunction and affected the pathogenicity but not the levels of mtDNA somatic mutations. A systemic loss of Parkin synergizes with mitochondrial dysfunction causing dopaminergic neuron death modeling PD pathogenic processes. [ABSTRACT FROM AUTHOR]
- Published
- 2015
- Full Text
- View/download PDF
17. Balanced Ero1 activation and inactivation establishes ER redox homeostasis.
- Author
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Kim S, Sideris DP, Sevier CS, and Kaiser CA
- Subjects
- Disulfides chemistry, Disulfides metabolism, Glutathione metabolism, Homeostasis, Oxidation-Reduction, Protein Disulfide-Isomerases genetics, Protein Disulfide-Isomerases metabolism, Saccharomyces cerevisiae genetics, Saccharomyces cerevisiae metabolism, Saccharomyces cerevisiae Proteins genetics, Endoplasmic Reticulum metabolism, Glycoproteins metabolism, Oxidoreductases Acting on Sulfur Group Donors metabolism, Saccharomyces cerevisiae Proteins metabolism
- Abstract
The endoplasmic reticulum (ER) provides an environment optimized for oxidative protein folding through the action of Ero1p, which generates disulfide bonds, and Pdi1p, which receives disulfide bonds from Ero1p and transfers them to substrate proteins. Feedback regulation of Ero1p through reduction and oxidation of regulatory bonds within Ero1p is essential for maintaining the proper redox balance in the ER. In this paper, we show that Pdi1p is the key regulator of Ero1p activity. Reduced Pdi1p resulted in the activation of Ero1p by direct reduction of Ero1p regulatory bonds. Conversely, upon depletion of thiol substrates and accumulation of oxidized Pdi1p, Ero1p was inactivated by both autonomous oxidation and Pdi1p-mediated oxidation of Ero1p regulatory bonds. Pdi1p responded to the availability of free thiols and the relative levels of reduced and oxidized glutathione in the ER to control Ero1p activity and ensure that cells generate the minimum number of disulfide bonds needed for efficient oxidative protein folding.
- Published
- 2012
- Full Text
- View/download PDF
18. Oxidative protein folding in the mitochondrial intermembrane space.
- Author
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Sideris DP and Tokatlidis K
- Subjects
- Disulfides chemistry, Disulfides metabolism, Humans, Mitochondrial Membrane Transport Proteins chemistry, Models, Molecular, Oxidation-Reduction, Mitochondrial Membrane Transport Proteins metabolism, Mitochondrial Membranes metabolism, Protein Folding
- Abstract
Disulfide bond formation is a crucial step for oxidative folding and necessary for the acquisition of a protein's native conformation. Introduction of disulfide bonds is catalyzed in specialized subcellular compartments and requires the coordinated action of specific enzymes. The intermembrane space of mitochondria has recently been found to harbor a dedicated machinery that promotes the oxidative folding of substrate proteins by shuttling disulfide bonds. The newly identified oxidative pathway consists of the redox-regulated receptor Mia40 and the sulfhydryl oxidase Erv1. Proteins destined to the intermembrane space are trapped by a disulfide relay mechanism that involves an electron cascade from the incoming substrate to Mia40, then on to Erv1, and finally to molecular oxygen via cytochrome c. This thiol-disulfide exchange mechanism is essential for the import and for maintaining the structural stability of the incoming precursors. In this review we describe the mechanistic parameters that define the interaction and oxidation of the substrate proteins in light of the recent publications in the mitochondrial oxidative folding field.
- Published
- 2010
- Full Text
- View/download PDF
19. Trapping oxidative folding intermediates during translocation to the intermembrane space of mitochondria: in vivo and in vitro studies.
- Author
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Sideris DP and Tokatlidis K
- Subjects
- Autoradiography, Electrophoresis, Electrophoresis, Polyacrylamide Gel, Intracellular Membranes metabolism, Models, Biological, Oxidation-Reduction, Protein Folding, Protein Transport physiology, Proteins chemistry, Yeasts metabolism, Mitochondria metabolism, Proteins metabolism
- Abstract
The MIA40 pathway is a novel import pathway in mitochondria specific for cysteine-rich proteins of the intermembrane space (IMS). The newly synthesised precursors are trapped in the IMS by a disulfide relay mechanism that involves introduction of disulfides from the sulfhydryl oxidase Erv1 to the redox-regulated import receptor Mia40 and then on to the substrate. This thiol-disulfide exchange mechanism is essential for the import and oxidative folding of the incoming cysteine-rich substrate proteins. In this chapter we will describe the experimental methods that have been developed in order to study and characterise disulfide-trapped intermediates in yeast mitochondria.
- Published
- 2010
- Full Text
- View/download PDF
20. ICPBCZin: a red emitting ratiometric fluorescent indicator with nanomolar affinity for Zn2+ ions.
- Author
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Roussakis E, Voutsadaki S, Pinakoulaki E, Sideris DP, Tokatlidis K, and Katerinopoulos HE
- Subjects
- Benzimidazoles chemical synthesis, Benzopyrans chemical synthesis, Cells, Cultured, Chelating Agents chemistry, Fluorescent Dyes chemical synthesis, Microscopy, Fluorescence, Spectrometry, Fluorescence, Benzimidazoles chemistry, Benzopyrans chemistry, Fluorescent Dyes chemistry, Zinc chemistry
- Abstract
A new fluorescent Zn2+ indicator, namely, ICPBCZin was synthesized and the spectral profile of its free and Zn2+ bound forms was studied. The newly synthesized zinc indicator incorporates as chromophore the chromeno [3',2':3,4]pyrido[1,2a] [1,3]benzimidazole moiety and belongs to the dicarboxylate-type of zinc probes. The compound is excited with visible light, exhibits high selectivity for zinc in the presence of calcium and other common biological ions, and its Zn2+ dissociation constant is 4.0 nM. Fluorescence spectra studies of ICPBCZin indicated a clear shift in its emission wavelength maxima upon Zn2+ binding, as it belongs to the class of Photoinduced Charge Transfer (PCT) indicators, along with changes in fluorescence intensity that enable the compound to be used as a ratiometric, visible-excitable Zn2+ probe.
- Published
- 2008
- Full Text
- View/download PDF
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