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  1. Article ; Online: Theta burst stimulation add on to dialectical behavioral therapy in borderline-personality-disorder: methods and design of a randomized, single-blind, placebo-controlled pilot trial.

    Kujovic, Milenko / Benz, Daniel / Riesbeck, Mathias / Bahr, Christian / Kriegs, Christian / Reinermann, Dirk / Jänner, Michaela / Neufang, Susanne / Margittai, Zsofia / Kamp, Daniel / Plewnia, Christian / Meisenzahl, Eva

    European archives of psychiatry and clinical neuroscience

    2023  Volume 274, Issue 1, Page(s) 87–96

    Abstract: Specialized psychotherapeutic treatments like dialectical behavioral therapy (DBT) are recommended as first treatment for borderline personality disorder (BPD). In recent years, studies have emerged that focus on repetitive transcranial magnetic ... ...

    Abstract Specialized psychotherapeutic treatments like dialectical behavioral therapy (DBT) are recommended as first treatment for borderline personality disorder (BPD). In recent years, studies have emerged that focus on repetitive transcranial magnetic stimulation (rTMS) in BPD. Both have independently demonstrated efficacy in the treatment of BPD. Intermitted theta burst stimulation (iTBS), a modified design of rTMS, is thought to increase the excitability of neurons and could be a supplement to psychotherapy in addition to being a standalone treatment. However, no studies to date have investigated the combination of DBT and rTMS/iTBS. This study protocol describes the methods and design of a randomized, single-blinded, sham-controlled clinical pilot study in which BPD patients will be randomly assigned to either iTBS or sham during four consecutive weeks (20 sessions in total) in addition to standardized DBT treatment. The stimulation will focus on the unilateral stimulation of the left dorsolateral prefrontal cortex (DLPFC), which plays an important role in the control of impulsivity and risk-taking. Primary outcome is the difference in borderline symptomatology, while secondary target criteria are depressive symptoms, general functional level, impulsivity and self-compassion. Statistical analysis of therapy response will be conducted by Mixed Model Repeated Measurement using a 2 × 2-factorial between-subjects design with the between-subject factor stimulation (TMS vs. Sham) and the within-subject factor time (T0 vs. T1). Furthermore, structural magnetic resonance imaging (MRI) will be conducted and analyzed. The study will provide evidence and insight on whether iTBS has an enhancing effect as add-on to DBT in BPD.Trial registration: drks.de (DRKS00020413) registered 13/01/2020.
    MeSH term(s) Humans ; Behavior Therapy ; Borderline Personality Disorder/therapy ; Personality ; Pilot Projects ; Prefrontal Cortex/physiology ; Single-Blind Method ; Transcranial Magnetic Stimulation/methods ; Treatment Outcome ; Randomized Controlled Trials as Topic
    Language English
    Publishing date 2023-09-15
    Publishing country Germany
    Document type Clinical Trial Protocol ; Journal Article
    ZDB-ID 1045583-8
    ISSN 1433-8491 ; 0175-758X ; 0940-1334
    ISSN (online) 1433-8491
    ISSN 0175-758X ; 0940-1334
    DOI 10.1007/s00406-023-01692-w
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Species-Specific Glucose-6-Phosphatase Activity in the Small Intestine-Studies in Three Different Mammalian Models.

    Varga, Viola / Murányi, Zsófia / Kurucz, Anita / Marcolongo, Paola / Benedetti, Angelo / Bánhegyi, Gábor / Margittai, Éva

    International journal of molecular sciences

    2019  Volume 20, Issue 20

    Abstract: Besides the liver, which has always been considered the major source of endogenous glucose production in all post-absorptive situations, kidneys and intestines can also produce glucose in blood, particularly during fasting and under protein feeding. ... ...

    Abstract Besides the liver, which has always been considered the major source of endogenous glucose production in all post-absorptive situations, kidneys and intestines can also produce glucose in blood, particularly during fasting and under protein feeding. However, observations gained in different experimental animals have given ambiguous results concerning the presence of the glucose-6-phosphatase system in the small intestine. The aim of this study was to better define the species-related differences of this putative gluconeogenic organ in glucose homeostasis. The components of the glucose-6-phosphatase system (i.e., glucose-6-phosphate transporter and glucose-6-phosphatase itself) were analyzed in homogenates or microsomal fractions prepared from the small intestine mucosae and liver of rats, guinea pigs, and humans. Protein and mRNA levels, as well as glucose-6-phosphatase activities, were detected. The results showed that the glucose-6-phosphatase system is poorly represented in the small intestine of rats; on the other hand, significant expressions of glucose-6-phosphate transporter and of the glucose-6-phosphatase were found in the small intestine of guinea pigs and homo sapiens. The activity of the recently described fructose-6-phosphate transporter-intraluminal hexose isomerase pathway was also present in intestinal microsomes from these two species. The results demonstrate that the gluconeogenic role of the small intestine is highly species-specific and presumably dependent on feeding behavior (e.g., fructose consumption) and the actual state of metabolism.
    MeSH term(s) Animals ; Fructose/metabolism ; Glucose-6-Phosphatase/genetics ; Glucose-6-Phosphatase/metabolism ; Guinea Pigs ; Humans ; Intestine, Small/enzymology ; Microsomes/enzymology ; Rats ; Species Specificity
    Chemical Substances Fructose (30237-26-4) ; Glucose-6-Phosphatase (EC 3.1.3.9)
    Language English
    Publishing date 2019-10-11
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2019364-6
    ISSN 1422-0067 ; 1422-0067 ; 1661-6596
    ISSN (online) 1422-0067
    ISSN 1422-0067 ; 1661-6596
    DOI 10.3390/ijms20205039
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  3. Article ; Online: The demise of preimplantation genetic testing for aneuploidy (PGT-A) in Hungary and its effect on patient care.

    Varga, Karolina / Tóth, Nikolett / Bogár, Éva B / Csontos, László / Szabó, Katalin / Debreceni, Diána / Margittai, Éva / Csenki, Marianna / Vereczkey, Attila

    European journal of medical genetics

    2019  Volume 62, Issue 8, Page(s) 103669

    Abstract: Preimplantation genetic testing for aneuploidy (PGT-A) is a suitable technique to identify euploid embryos, which have the highest potential to implant, thus increase the chance of a healthy live birth. The main indications of PGT-A are advanced maternal ...

    Abstract Preimplantation genetic testing for aneuploidy (PGT-A) is a suitable technique to identify euploid embryos, which have the highest potential to implant, thus increase the chance of a healthy live birth. The main indications of PGT-A are advanced maternal age, repeated implantation failure, repeated miscarriages and severe male infertility. Several studies have already proven that testing embryos for genetic abnormalities in the above cases results in higher implantation rate and reduced number of pregnancy loss. In spite of these - due to a legislative change in Hungary in 2015 - PGT-A was reclassified as an experimental procedure and its use became banned throughout the country. For this reason, after 4 years of successful practice, Hungarian patients were not able to participate in IVF procedure combined with PGT-A anymore. In this retrospective analysis, efficacy of PGT-A-based embryo selection was evaluated and was compared to the conventional morphology-based selection (MBS) in patients with advanced maternal age, between 2013 and 2017 at our private fertility clinic. PGT-A was performed with array comparative genomic hybridization. We found that implantation rate was significantly higher (43.62% vs. 27.88%; p = 0.0208) and miscarriage rate was significantly lower (17.07% vs. 37.93%; p = 0.0492) in the PGT-A group compared to the MBS group from 2013 to 2015. These outcomes were achieved with a significantly lower number of transferred embryos in the PGT-A group (1.25 vs. 1.58; p = 0.0003). In 2016-2017, the number of transferred embryos were significantly reduced in the MBS group as well (1.14 vs. 1.58; p < 0.0001). However, outcomes of the IVF treatments did not change significantly compared to the previous two years (2013-2015). Our results imply that PGT-A-based embryo selection is more efficient than morphology-based selection in patients with advanced maternal age. Therefore, prohibition of the use of PGT-A had significant consequences on the efficiency and safety of IVF treatment in the country.
    MeSH term(s) Abortion, Spontaneous/diagnosis ; Abortion, Spontaneous/epidemiology ; Abortion, Spontaneous/genetics ; Abortion, Spontaneous/pathology ; Adult ; Aneuploidy ; Blastocyst/metabolism ; Blastocyst/pathology ; Comparative Genomic Hybridization ; Embryo Transfer/methods ; Female ; Fertilization in Vitro/methods ; Humans ; Hungary/epidemiology ; Patient Care ; Pregnancy ; Preimplantation Diagnosis
    Language English
    Publishing date 2019-05-10
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 2184135-4
    ISSN 1878-0849 ; 1769-7212
    ISSN (online) 1878-0849
    ISSN 1769-7212
    DOI 10.1016/j.ejmg.2019.05.008
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  4. Article ; Online: Mevalonate Pathway-mediated ER Homeostasis Is Required for Haploid Stability in Human Somatic Cells.

    Yaguchi, Kan / Sato, Kimino / Yoshizawa, Koya / Mikami, Daisuke / Yuyama, Kohei / Igarashi, Yasuyuki / Banhegyi, Gabor / Margittai, Eva / Uehara, Ryota

    Cell structure and function

    2020  Volume 46, Issue 1, Page(s) 1–9

    Abstract: The somatic haploidy is unstable in diplontic animals, but cellular processes determining haploid stability remain elusive. Here, we found that inhibition of mevalonate pathway by pitavastatin, a widely used cholesterol-lowering drug, drastically ... ...

    Abstract The somatic haploidy is unstable in diplontic animals, but cellular processes determining haploid stability remain elusive. Here, we found that inhibition of mevalonate pathway by pitavastatin, a widely used cholesterol-lowering drug, drastically destabilized the haploid state in HAP1 cells. Interestingly, cholesterol supplementation did not restore haploid stability in pitavastatin-treated cells, and cholesterol inhibitor U18666A did not phenocopy haploid destabilization. These results ruled out the involvement of cholesterol in haploid stability. Besides cholesterol perturbation, pitavastatin induced endoplasmic reticulum (ER) stress, the suppression of which by a chemical chaperon significantly restored haploid stability in pitavastatin-treated cells. Our data demonstrate the involvement of the mevalonate pathway in the stability of the haploid state in human somatic cells through managing ER stress, highlighting a novel link between ploidy and ER homeostatic control.Key words: haploid, ER stress, Mevalonate pathway.
    MeSH term(s) Cell Line ; Cholesterol ; Endoplasmic Reticulum Stress ; Haploidy ; Homeostasis ; Humans
    Chemical Substances Cholesterol (97C5T2UQ7J)
    Language English
    Publishing date 2020-12-22
    Publishing country Japan
    Document type Journal Article
    ZDB-ID 197293-5
    ISSN 1347-3700 ; 0386-7196
    ISSN (online) 1347-3700
    ISSN 0386-7196
    DOI 10.1247/csf.20055
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Species-Specific Glucose-6-Phosphatase Activity in the Small Intestine—Studies in Three Different Mammalian Models

    Viola Varga / Zsófia Murányi / Anita Kurucz / Paola Marcolongo / Angelo Benedetti / Gábor Bánhegyi / Éva Margittai

    International Journal of Molecular Sciences, Vol 20, Iss 20, p

    2019  Volume 5039

    Abstract: Besides the liver, which has always been considered the major source of endogenous glucose production in all post-absorptive situations, kidneys and intestines can also produce glucose in blood, particularly during fasting and under protein feeding. ... ...

    Abstract Besides the liver, which has always been considered the major source of endogenous glucose production in all post-absorptive situations, kidneys and intestines can also produce glucose in blood, particularly during fasting and under protein feeding. However, observations gained in different experimental animals have given ambiguous results concerning the presence of the glucose-6-phosphatase system in the small intestine. The aim of this study was to better define the species-related differences of this putative gluconeogenic organ in glucose homeostasis. The components of the glucose-6-phosphatase system (i.e., glucose-6-phosphate transporter and glucose-6-phosphatase itself) were analyzed in homogenates or microsomal fractions prepared from the small intestine mucosae and liver of rats, guinea pigs, and humans. Protein and mRNA levels, as well as glucose-6-phosphatase activities, were detected. The results showed that the glucose-6-phosphatase system is poorly represented in the small intestine of rats; on the other hand, significant expressions of glucose-6-phosphate transporter and of the glucose-6-phosphatase were found in the small intestine of guinea pigs and homo sapiens. The activity of the recently described fructose-6-phosphate transporter−intraluminal hexose isomerase pathway was also present in intestinal microsomes from these two species. The results demonstrate that the gluconeogenic role of the small intestine is highly species-specific and presumably dependent on feeding behavior (e.g., fructose consumption) and the actual state of metabolism.
    Keywords glucose-6-phosphatase ; glucose-6-phosphate transporter ; small intestine ; endoplasmic reticulum ; fructose ; Biology (General) ; QH301-705.5 ; Chemistry ; QD1-999
    Subject code 670
    Language English
    Publishing date 2019-10-01T00:00:00Z
    Publisher MDPI AG
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  6. Article ; Online: Arterial Tortuosity Syndrome: An Ascorbate Compartmentalization Disorder?

    Boel, Annekatrien / Veszelyi, Krisztina / Németh, Csilla E / Beyens, Aude / Willaert, Andy / Coucke, Paul / Callewaert, Bert / Margittai, Éva

    Antioxidants & redox signaling

    2019  Volume 34, Issue 11, Page(s) 875–889

    Abstract: Significance: ...

    Abstract Significance:
    MeSH term(s) Animals ; Arteries/abnormalities ; Arteries/metabolism ; Arteries/pathology ; Ascorbic Acid/genetics ; Ascorbic Acid/metabolism ; Ascorbic Acid/therapeutic use ; Elastic Tissue/metabolism ; Elastic Tissue/pathology ; Glucose Transport Proteins, Facilitative/genetics ; Homeostasis/genetics ; Humans ; Joint Instability/genetics ; Joint Instability/metabolism ; Joint Instability/pathology ; Joint Instability/therapy ; Mitochondria/drug effects ; Mitochondria/genetics ; Mutation/genetics ; Oxidation-Reduction ; Skin Diseases, Genetic/genetics ; Skin Diseases, Genetic/metabolism ; Skin Diseases, Genetic/pathology ; Skin Diseases, Genetic/therapy ; Vascular Malformations/genetics ; Vascular Malformations/metabolism ; Vascular Malformations/pathology ; Vascular Malformations/therapy
    Chemical Substances Glucose Transport Proteins, Facilitative ; SLC2A10 protein, human ; Ascorbic Acid (PQ6CK8PD0R)
    Language English
    Publishing date 2019-11-14
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1483836-9
    ISSN 1557-7716 ; 1523-0864
    ISSN (online) 1557-7716
    ISSN 1523-0864
    DOI 10.1089/ars.2019.7843
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  7. Article ; Online: Glucose Transport and Transporters in the Endomembranes.

    Lizák, Beáta / Szarka, András / Kim, Yejin / Choi, Kyu-Sung / Németh, Csilla E / Marcolongo, Paola / Benedetti, Angelo / Bánhegyi, Gábor / Margittai, Éva

    International journal of molecular sciences

    2019  Volume 20, Issue 23

    Abstract: Glucose is a basic nutrient in most of the creatures; its transport through biological membranes is an absolute requirement of life. This role is fulfilled by glucose transporters, mediating the transport of glucose by facilitated diffusion or by ... ...

    Abstract Glucose is a basic nutrient in most of the creatures; its transport through biological membranes is an absolute requirement of life. This role is fulfilled by glucose transporters, mediating the transport of glucose by facilitated diffusion or by secondary active transport. GLUT (glucose transporter) or SLC2A (Solute carrier 2A) families represent the main glucose transporters in mammalian cells, originally described as plasma membrane transporters. Glucose transport through intracellular membranes has not been elucidated yet; however, glucose is formed in the lumen of various organelles. The glucose-6-phosphatase system catalyzing the last common step of gluconeogenesis and glycogenolysis generates glucose within the lumen of the endoplasmic reticulum. Posttranslational processing of the oligosaccharide moiety of glycoproteins also results in intraluminal glucose formation in the endoplasmic reticulum (ER) and Golgi. Autophagic degradation of polysaccharides, glycoproteins, and glycolipids leads to glucose accumulation in lysosomes. Despite the obvious necessity, the mechanism of glucose transport and the molecular nature of mediating proteins in the endomembranes have been hardly elucidated for the last few years. However, recent studies revealed the intracellular localization and functional features of some glucose transporters; the aim of the present paper was to summarize the collected knowledge.
    MeSH term(s) Animals ; Cell Membrane/metabolism ; Endoplasmic Reticulum/metabolism ; Glucose/metabolism ; Glucose Transport Proteins, Facilitative/metabolism ; Glucose-6-Phosphatase/metabolism ; Golgi Apparatus/metabolism ; Humans ; Sodium-Glucose Transport Proteins/metabolism
    Chemical Substances Glucose Transport Proteins, Facilitative ; Sodium-Glucose Transport Proteins ; Glucose-6-Phosphatase (EC 3.1.3.9) ; Glucose (IY9XDZ35W2)
    Language English
    Publishing date 2019-11-24
    Publishing country Switzerland
    Document type Journal Article ; Review
    ZDB-ID 2019364-6
    ISSN 1422-0067 ; 1422-0067 ; 1661-6596
    ISSN (online) 1422-0067
    ISSN 1422-0067 ; 1661-6596
    DOI 10.3390/ijms20235898
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  8. Article ; Online: A Systems Biological View of Life-and-Death Decision with Respect to Endoplasmic Reticulum Stress-The Role of PERK Pathway.

    Márton, Margita / Kurucz, Anita / Lizák, Beáta / Margittai, Éva / Bánhegyi, Gábor / Kapuy, Orsolya

    International journal of molecular sciences

    2017  Volume 18, Issue 1

    Abstract: Accumulation of misfolded/unfolded proteins in the endoplasmic reticulum (ER) leads to the activation of three branches (Protein kinase (RNA)-like endoplasmic reticulum kinase [PERK], Inositol requiring protein 1 [IRE-1] and Activating trascription ... ...

    Abstract Accumulation of misfolded/unfolded proteins in the endoplasmic reticulum (ER) leads to the activation of three branches (Protein kinase (RNA)-like endoplasmic reticulum kinase [PERK], Inositol requiring protein 1 [IRE-1] and Activating trascription factor 6 [ATF6], respectively) of unfolded protein response (UPR). The primary role of UPR is to try to drive back the system to the former or a new homeostatic state by self-eating dependent autophagy, while excessive level of ER stress results in apoptotic cell death. Our study focuses on the role of PERK- and IRE-1-induced arms of UPR in life-or-death decision. Here we confirm that silencing of PERK extends autophagy-dependent survival, whereas the IRE-1-controlled apoptosis inducer is downregulated during ER stress. We also claim that the proper order of surviving and self-killing mechanisms is controlled by a positive feedback loop between PERK and IRE-1 branches. This regulatory network makes possible a smooth, continuous activation of autophagy with respect to ER stress, while the induction of apoptosis is irreversible and switch-like. Using our knowledge of molecular biological techniques and systems biological tools we give a qualitative description about the dynamical behavior of PERK- and IRE-1-controlled life-or-death decision. Our model claims that the two arms of UPR accomplish an altered upregulation of autophagy and apoptosis inducers during ER stress. Since ER stress is tightly connected to aging and age-related degenerative disorders, studying the signaling pathways of UPR and their role in maintaining ER proteostasis have medical importance.
    MeSH term(s) Apoptosis/genetics ; Autophagy/genetics ; Blotting, Western ; Cell Survival/genetics ; Endoplasmic Reticulum Stress/genetics ; Endoribonucleases/genetics ; Endoribonucleases/metabolism ; Feedback, Physiological ; Gene Expression ; HEK293 Cells ; Homeostasis/genetics ; Humans ; Models, Biological ; Protein-Serine-Threonine Kinases/genetics ; Protein-Serine-Threonine Kinases/metabolism ; RNA Interference ; Reverse Transcriptase Polymerase Chain Reaction ; Signal Transduction/genetics ; Systems Biology/methods ; Unfolded Protein Response/genetics ; eIF-2 Kinase/genetics ; eIF-2 Kinase/metabolism
    Chemical Substances EIF2AK3 protein, human (EC 2.7.11.1) ; ERN1 protein, human (EC 2.7.11.1) ; Protein-Serine-Threonine Kinases (EC 2.7.11.1) ; eIF-2 Kinase (EC 2.7.11.1) ; Endoribonucleases (EC 3.1.-)
    Language English
    Publishing date 2017-01-05
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2019364-6
    ISSN 1422-0067 ; 1422-0067 ; 1661-6596
    ISSN (online) 1422-0067
    ISSN 1422-0067 ; 1661-6596
    DOI 10.3390/ijms18010058
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  9. Article ; Online: Composition of the redox environment of the endoplasmic reticulum and sources of hydrogen peroxide.

    Margittai, Éva / Enyedi, Balázs / Csala, Miklós / Geiszt, Miklós / Bánhegyi, Gábor

    Free radical biology & medicine

    2015  Volume 83, Page(s) 331–340

    Abstract: The endoplasmic reticulum (ER) is a metabolically active organelle, which has a central role in proteostasis by translating, modifying, folding, and occasionally degrading secretory and membrane proteins. The lumen of the ER represents a separate ... ...

    Abstract The endoplasmic reticulum (ER) is a metabolically active organelle, which has a central role in proteostasis by translating, modifying, folding, and occasionally degrading secretory and membrane proteins. The lumen of the ER represents a separate compartment of the eukaryotic cell, with a characteristic proteome and metabolome. Although the redox metabolome and proteome of the compartment have not been holistically explored, it is evident that proper redox conditions are necessary for the functioning of many luminal pathways. These redox conditions are defined by local oxidoreductases and the membrane transport of electron donors and acceptors. The main electron carriers of the compartment are identical with those of the other organelles: glutathione, pyridine and flavin nucleotides, ascorbate, and others. However, their composition, concentration, and redox state in the ER lumen can be different from those observed in other compartments. The terminal oxidases of oxidative protein folding generate and maintain an "oxidative environment" by oxidizing protein thiols and producing hydrogen peroxide. ER-specific mechanisms reutilize hydrogen peroxide as an electron acceptor of oxidative folding. These mechanisms, together with membrane and kinetic barriers, guarantee that redox systems in the reduced or oxidized state can be present simultaneously in the lumen. The present knowledge on the in vivo conditions of ER redox is rather limited; development of new genetically encoded targetable sensors for the measurement of the luminal state of redox systems other than thiol/disulfide will contribute to a better understanding of ER redox homeostasis.
    MeSH term(s) Animals ; Endoplasmic Reticulum/physiology ; Homeostasis/physiology ; Humans ; Hydrogen Peroxide/metabolism ; Oxidants/metabolism ; Oxidation-Reduction
    Chemical Substances Oxidants ; Hydrogen Peroxide (BBX060AN9V)
    Language English
    Publishing date 2015-06
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 807032-5
    ISSN 1873-4596 ; 0891-5849
    ISSN (online) 1873-4596
    ISSN 0891-5849
    DOI 10.1016/j.freeradbiomed.2015.01.032
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  10. Article ; Online: Oxidative folding in the endoplasmic reticulum: towards a multiple oxidant hypothesis?

    Margittai, Eva / Bánhegyi, Gábor

    FEBS letters

    2010  Volume 584, Issue 14, Page(s) 2995–2998

    Abstract: Oxidative protein folding in the luminal compartment of the endoplasmic reticulum is thought to be mediated by a proteinaceous electron relay system composed by PDI and ER oxidoreductin 1 (Ero1), transferring electrons from the cysteinyl residues of ... ...

    Abstract Oxidative protein folding in the luminal compartment of the endoplasmic reticulum is thought to be mediated by a proteinaceous electron relay system composed by PDI and ER oxidoreductin 1 (Ero1), transferring electrons from the cysteinyl residues of substrate proteins to oxygen. However, recent observations revealed that Ero1 isoforms are dispensable. Endoplasmic reticulum is known as a generator and accumulator of low molecular weight oxidants; some of them have already been shown to promote oxidative folding. On the basis of these observations a new theory of oxidative folding is proposed where the oxidative power is provided by the stochastic contribution of prooxidants.
    MeSH term(s) Animals ; Endoplasmic Reticulum/metabolism ; Models, Biological ; Oxidants/metabolism ; Oxidation-Reduction ; Oxides/metabolism ; Oxygen/metabolism ; Protein Folding ; Protein Isoforms/metabolism ; Reactive Oxygen Species/metabolism
    Chemical Substances Oxidants ; Oxides ; Protein Isoforms ; Reactive Oxygen Species ; Oxygen (S88TT14065)
    Language English
    Publishing date 2010-07-16
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 212746-5
    ISSN 1873-3468 ; 0014-5793
    ISSN (online) 1873-3468
    ISSN 0014-5793
    DOI 10.1016/j.febslet.2010.05.055
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