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1.
Chemphyschem ; 24(23): e202300534, 2023 Dec 01.
Artigo em Inglês | MEDLINE | ID: mdl-37713246

RESUMO

OH⋅-induced oxidation products of DNA nucleosides and nucleotides have been structurally characterized by collision-induced dissociation tandem mass spectrometry (CID-MS2 ) and Infrared Multiple Photon Dissociation (IRMPD) spectroscopy. CID-MS2 results have shown that the addition of one oxygen atom occurs on the nucleobase moiety. The gas-phase geometries of +16 mass increment products of 2'-deoxyadenosine (dA(O)H+ ), 2'-deoxyadenosine 5'-monophosphate (dAMP(O)H+ ), 2'-deoxycytidine (dC(O)H+ ), and 2'-deoxycytidine 5'-monophosphate (dCMP(O)H+ ) are extensively investigated by IRMPD spectroscopy and quantum-chemical calculations. We show that a carbonyl group is formed at the C8 position after oxidation of 2'-deoxyadenosine and its monophosphate derivative. For 2'-deoxycytidine and its monophosphate derivative, the oxygen atom is added to the C5 position to form a C-OH group. IRMPD spectroscopy has been employed for the first time to provide direct structural information on oxidative lesions in DNA model systems.


Assuntos
Nucleotídeos , Espectrometria de Massas em Tandem , Oxigênio , DNA/química , Desoxicitidina , Análise Espectral , Espectrofotometria Infravermelho/métodos
2.
J Phys Chem B ; 126(48): 10055-10068, 2022 12 08.
Artigo em Inglês | MEDLINE | ID: mdl-36417492

RESUMO

Reactive oxygen species (ROS) such as hydrogen peroxide (H2O2) and the hydroxyl radical (•OH) have specific functions in biological processes, while their uncontrolled production and reactivity are known to be determining factors in pathophysiology. Methionine (Met) residues act as endogenous antioxidants, when they are oxidized into methionine sulfoxide (MetSO), thus depleting ROS and protecting the protein. We employed tandem mass spectrometry combined with IR multiple photon dissociation spectroscopy to study the oxidation induced by OH radicals produced by γ radiolysis on model cyclic dipeptides c(LMetLMet), c(LMetDMet), and c(GlyMet). Our aim was to characterize the geometries of the oxidized peptides in the gas phase and to understand the relationship between the structure of the 2-center 3-electron (2c-3e) free radical formed in the first step of the oxidation process and the final compound. Density functional theory calculations were performed to characterize the lowest energy structures of the final product of oxidation and to interpret the IR spectra. Collision-induced dissociation tandem mass spectrometry (CID-MS2) experiments of oxidized c(LMetLMet)H+ and c(LMetDMet)H+ led to the loss of one or two oxidized sulfenic acid molecules, indicating that the addition of one or two oxygen atoms occurs on the sulfur atom of both methionine side chains and no sulfone formation was observed. The CID-MS2 fragmentation mass spectrum of oxidized c(GlyMet)H+ showed only the loss of one oxidized sulfenic acid molecule. Thus, the final products of oxidation are the same regardless of the structure of the precursor sulfur-centered free radical.


Assuntos
Dipeptídeos , Elétrons , Ácidos Sulfênicos , Peróxido de Hidrogênio , Metionina , Análise Espectral , Enxofre
3.
Int J Mol Sci ; 23(2)2022 Jan 11.
Artigo em Inglês | MEDLINE | ID: mdl-35054950

RESUMO

Neutrophils play a very key role in the human immune defense against pathogenic infections. The predominant players in this role during the activation of neutrophils are the release of cytotoxic agents stored in the granules and secretory vesicles and the massive production of reactive oxygen species (ROS) initiated by the enzyme NADPH oxidase. In addition, in living organisms, cells are continuously exposed to endogenous (inflammations, elevated neutrophil presence in the vicinity) and exogenous ROS at low and moderate levels (travels by plane, radiotherapy, space irradiation, blood banking, etc.). To study these effects, we used ROS induced by gamma radiation from low (0.2 Gy) to high (25 Gy) dose levels on PLB-985 cells from a myeloid cell line differentiated to neutrophil-like cells that are considered a good alternative to neutrophils. We determined a much longer lifetime of PLB-985 cells than that of neutrophils, which, as expected, decreased by increasing the irradiation dose. In the absence of any secondary stimulus, a very low production of ROS is detected with no significant difference between irradiated and non-irradiated cells. However, in phagocytosing cells, irradiation doses above 2 Gy enhanced oxidative burst in PLB-985 cells. Whatever the irradiation dose, NADPH oxidase devoid of its cytosolic regulatory units is observed at the plasma membrane in irradiated PLB-985 cells. This result is different from that observed for irradiated neutrophils in which irradiation also induced a translocation of regulatory subunits suggesting that the signal transduction mechanism or pathway operate differently in both cells.


Assuntos
Biomarcadores , Membrana Celular/metabolismo , Citocromos b/metabolismo , Estresse Oxidativo , Fagócitos/metabolismo , Sobrevivência Celular/efeitos da radiação , Relação Dose-Resposta à Radiação , Ativação Enzimática , Raios gama , Humanos , NADPH Oxidases/metabolismo , Neutrófilos/metabolismo , Fagócitos/imunologia , Fagócitos/efeitos da radiação , Transporte Proteico , Espécies Reativas de Oxigênio/imunologia , Espécies Reativas de Oxigênio/metabolismo , Explosão Respiratória
4.
Int J Radiat Biol ; 98(3): 297-302, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-34402396

RESUMO

PURPOSE: Pay tribute to Christiane Ferradini and highlight the importance of her work as a scientist. CONCLUSIONS: Christiane Ferradini was born in 1924 in the south of France. She graduated from the Paul Sabatier University in Toulouse, France. In 1947, she joined the Curie Laboratory of the Radium Institute (which was then under the leadership of Madame Irène Joliot-Curie) to pursue her doctoral research. After her defence in 1955, she commenced her journey dedicated to the advancement of science. She became an exceptional teacher. She led a research group that contributed, through many fruitful collaborations, to the opening of a new chapter in radiation biology and medicine. Together they shed light on free radical formation and their reactions with biomolecules. Christiane published a total of 190 scientific articles and 9 books. She died in 2002.


Assuntos
Radiobiologia , Pesquisadores , Mulheres Trabalhadoras , Feminino , França , História do Século XX , Humanos , Radiobiologia/história , Pesquisadores/história , Mulheres Trabalhadoras/história
5.
Free Radic Biol Med ; 164: 76-84, 2021 02 20.
Artigo em Inglês | MEDLINE | ID: mdl-33387605

RESUMO

Neutrophils are key cells from the innate immune system that destroy invading bacteria or viruses, thanks mainly to the non-mitochondrial reactive oxygen species (ROS) generated by the enzyme NADPH oxidase. Our aim was to study the response of neutrophils to situations of oxidative stress with emphasis on the impact on the NADPH oxidase complex. To mimic oxidative stress, we used gamma irradiation that generated ROS (OH•, O2•- and H2O2) in a quantitative controlled manner. We showed that, although irradiation induces shorter half-lives of neutrophil (reduced by at least a factor of 2), it triggers a pre-activation of surviving neutrophils. This is detectable by the production of a small but significant amount of superoxide anions, proportional to the dose (about 3 times that of sham). Investigations at the molecular level showed that this ROS increase was generated by the NADPH oxidase enzyme after neutrophils irradiation. The NADPH oxidase complex undergoes an incomplete assembly which includes p47phox and p67phox but excludes the G-protein Rac. Importantly, this irradiation-induced pre-activation is capable of considerably improving neutrophil reactivity. Indeed, we have observed that this leads to an increase in the production of ROS and the capacity of phagocytosis, leading to the conclusion that radiation induced ROS clearly behave as neutrophil primers.


Assuntos
NADPH Oxidases , Neutrófilos , Radiação , Espécies Reativas de Oxigênio , Humanos , Peróxido de Hidrogênio , NADPH Oxidases/genética , Fosfoproteínas , Superóxidos
6.
Biochim Biophys Acta Gen Subj ; 1865(1): 129767, 2021 01.
Artigo em Inglês | MEDLINE | ID: mdl-33141062

RESUMO

BACKGROUND: The production of superoxide anions (O2•-) by the phagocyte NADPH oxidase complex has a crucial role in the destruction of pathogens in innate immunity. Majority of in vitro studies on the functioning of NADPH oxidase indirectly follows the enzymatic reaction by the superoxide reduction of cytochrome c (cyt c). Only few reports mention the alternative approach consisting in measuring the NADPH consumption rate. When using membrane vesicles of human neutrophils, the enzyme specific activity is generally found twice higher by monitoring the NADPH oxidation than by measuring the cyt c reduction. Up to now, the literature provides only little explanations about such discrepancy despite the critical importance to quantify the exact enzyme activity. METHODS: We deciphered the reasons of this disparity in studying the role of key parameters, including. cyt c and arachidonic acid concentrations, in conjunction with an ionophore, a detergent and using Clark electrode to measure the O2 consumption rates. RESULTS: Our results show that the O2•- low permeability of the vesicle membrane as well as secondary reactions (O2•- and H2O2 disproportionations) are strong clues to shed light on this inconsistency. CONCLUSION AND GENERAL SIGNIFICANCE: These results altogether indicate that the cyt c reduction method underestimates the accurate Nox2 activity.


Assuntos
NADPH Oxidase 2/metabolismo , Ácido Araquidônico/metabolismo , Células Cultivadas , Citocromos c/metabolismo , Humanos , Peróxido de Hidrogênio/metabolismo , NADP/metabolismo , Neutrófilos/metabolismo , Oxirredução , Consumo de Oxigênio
7.
J Struct Biol ; 210(2): 107478, 2020 05 01.
Artigo em Inglês | MEDLINE | ID: mdl-32087239

RESUMO

L-Lactate dehydrogenase (LDH) is a model protein allowing to shed light on the fundamental molecular mechanisms that drive the acquisition, evolution and regulation of enzyme properties. In this study, we test the hypothesis of a link between thermal stability of LDHs and their capacity against unfolding induced by reactive oxygen species (ROS) generated by γ-rays irradiation. By using circular dichroism spectroscopy, we analysed that high thermal stability of a thermophilic LDH favours strong resistance against ROS-induced unfolding, in contrast to its psychrophilic and mesophilic counterparts that are less resistant. We suggest that a protein's phenotype linking strong thermal stability and resistance against ROS damages would have been a selective evolutionary advantage. We also find that the enzymatic activity of the thermophilic LDH that is strongly resistant against ROS-unfolding is very sensitive to inactivation by irradiation. To address this counter-intuitive observation, we combined mass spectrometry analyses and enzymatic activity measurements. We demonstrate that the dramatic change on LDH activity was linked to remote chemical modifications away from the active site, that change the equilibrium between low-affinity tense (T-inactive) and high-affinity relaxed (R-active) forms. We found the T-inactive thermophilic enzyme obtained after irradiation can recover its LDH activity by addition of the allosteric effector 1, 6 fructose bis phosphate. We analyse our data within the general framework of allosteric regulation, which requires that an enzyme in solution populates a large diversity of dynamically-interchanging conformations. Our work demonstrates that the radiation-induced inactivation of an enzyme is controlled by its dynamical properties.


Assuntos
L-Lactato Desidrogenase/metabolismo , Regulação Alostérica , Sítios de Ligação , Domínio Catalítico , Radicais Livres/química , Cinética , L-Lactato Desidrogenase/genética , Estresse Oxidativo/genética , Estresse Oxidativo/fisiologia , Relação Estrutura-Atividade
8.
J Phys Chem B ; 123(43): 9087-9097, 2019 10 31.
Artigo em Inglês | MEDLINE | ID: mdl-31577444

RESUMO

The two inverse peptides methionine-valine (Met-Val) and valine-methionine (Val-Met) are investigated in an oxidative radiolysis process in water. The OH radical yields products with very different absorption spectra and concentration effects: Met-Val yields one main product with a band at about 400 nm and other products at higher energies; there is no concentration effect. Val-Met yields at least three products, with a striking concentration effect. Molecular simulations are performed with a combination of the Monte Carlo, density functional theory, and reaction field methods. The simulation of the possible transients enables an interpretation of the radiolysis: (1) Met-Val undergoes an H atom uptake leaving mainly a neutral radical with a 2-center-3-electron (2c-3e) SN bond, which cannot dimerize. Other radicals are present at higher energies. (2) Val-Met undergoes mainly an electron uptake leaving a cation monomer with a (2c-3e) SO bond and a cation dimer with a (2c-3e) SS bond. At higher energies, neutral radicals are possible. This cation monomer can transfer a proton toward a neutral peptide, leaving a neutral radical.


Assuntos
Dipeptídeos/química , Metionina/química , Valina/química , Cátions/química , Dipeptídeos/efeitos da radiação , Radicais Livres/química , Metionina/efeitos da radiação , Modelos Químicos , Estrutura Molecular , Oxirredução , Radiólise de Impulso , Valina/efeitos da radiação
9.
Methods Mol Biol ; 1982: 75-101, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-31172467

RESUMO

The NADPH oxidase NOX2 complex consists of assembled cytosolic and redox membrane proteins. In mammalian cells, natural arachidonic acid (cis-AA), released by activated phospholipase-A2, plays an important role in the activation of the NADPH oxidase, but the mechanism of action of cis-AA is still a matter of debate. In cell-free systems, cis-AA is commonly used for activation although its structural effects are still unclear. Undoubtedly cis-AA participates in the synergistic multi-partner assembly that can be hardly studied at the molecular level in vivo due to cellular complexity. The capacity of this anionic amphiphilic fatty acid to activate the oxidase is mainly explained by its ability to disrupt intramolecular bonds, mimicking phosphorylation events in cell signaling and therefore allowing protein-protein interactions. Interestingly the geometric isomerism of the fatty acid and its purity are crucial for optimal superoxide production in cell-free assays. Indeed, optimal NADPH oxidase assembly was hampered by the substitution of the cis form by the trans forms of AA isomers (Souabni et al., BBA-Biomembranes 1818:2314-2324, 2012). Structural analysis of the changes induced by these two compounds, by circular dichroism and by biochemical methods, revealed differences in the interaction between subunits. We describe how the specific geometry of AA plays an important role in the activation of the NOX2 complex.


Assuntos
Ácido Araquidônico/metabolismo , NADPH Oxidases/metabolismo , Fagócitos/enzimologia , Ácido Araquidônico/química , Fracionamento Celular , Membrana Celular/enzimologia , Membrana Celular/metabolismo , Sistema Livre de Células , Colorimetria , Ativação Enzimática , Isomerismo , Estrutura Molecular , NADPH Oxidases/antagonistas & inibidores , NADPH Oxidases/química , NADPH Oxidases/isolamento & purificação , Neutrófilos/enzimologia , Fagócitos/imunologia , Proteínas Recombinantes de Fusão , Análise Espectral
10.
Phys Chem Chem Phys ; 20(21): 14927-14937, 2018 May 30.
Artigo em Inglês | MEDLINE | ID: mdl-29786710

RESUMO

In irradiated DNA, by the base-to-base and backbone-to-base hole transfer processes, the hole (i.e., the unpaired spin) localizes on the most electropositive base, guanine. Phosphate radicals formed via ionization events in the DNA-backbone must play an important role in the backbone-to-base hole transfer process. However, earlier studies on irradiated hydrated DNA, on irradiated DNA-models in frozen aqueous solution and in neat dimethyl phosphate showed the formation of carbon-centered radicals and not phosphate radicals. Therefore, to model the backbone-to-base hole transfer process, we report picosecond pulse radiolysis studies of the reactions between H2PO4˙ with the DNA bases - G, A, T, and C in 6 M H3PO4 at 22 °C. The time-resolved observations show that in 6 M H3PO4, H2PO4˙ causes the one-electron oxidation of adenine, guanine and thymine, by forming the cation radicals via a single electron transfer (SET) process; however, the rate constant of the reaction of H2PO4˙ with cytosine is too low (<107 L mol-1 s-1) to be measured. The rates of these reactions are influenced by the protonation states and the reorganization energies of the base radicals and of the phosphate radical in 6 M H3PO4.


Assuntos
DNA/química , Fosfatos/química , Sequência de Bases , Citosina/química , Radicais Livres/química , Cinética , Oxirredução , Termodinâmica
11.
Mech Ageing Dev ; 172: 30-34, 2018 06.
Artigo em Inglês | MEDLINE | ID: mdl-29103982

RESUMO

The role of NADPH oxidase in ageing is debated because of the dual roles of free radicals, toxic though necessary. In this paper we summarize some results about two aspects linked to the regulation of the activity of phagocyte NADPH oxidase (Nox2), encountered frequently in elderly people: inflammation and hypercholesterolemia. In the presence of a high amount of reactive oxygen species (ROS) created by itself or by any other source, the enzyme activity is mostly lowered. Oxidation of the membrane and/or of one of the cytosolic partners could be responsible for this loss of activity. However using a cell free system, we had also shown that a low amount of ROS could activate this enzyme. Similarly, cholesterol has a similar dual role, either activating or inhibiting. In in vitro cell free system with neutrophil membranes from healthy donors, the addition, as well as the removal of cholesterol, diminishes the Nox2 activity. The activity of Nox2 is lowered in neutrophils of untreated hypercholesterolemic patients. Finally oxysterols (25-hydroxy-cholesterol or 5α, 6α - epoxy-cholesterol) do not induce effects different from that of non-oxidized cholesterol. These findings are in agreement with the Janus role of NADPH oxidase, the main source of non-mitochondrial ROS.


Assuntos
Envelhecimento/metabolismo , NADPH Oxidase 2/metabolismo , Estresse Oxidativo , Fagócitos/enzimologia , Espécies Reativas de Oxigênio/metabolismo , Envelhecimento/patologia , Animais , Membrana Celular/enzimologia , Membrana Celular/patologia , Humanos , Hipercolesterolemia/enzimologia , Hipercolesterolemia/patologia , Inflamação/enzimologia , Inflamação/patologia , Oxirredução , Oxisteróis/metabolismo , Fagócitos/patologia
12.
Free Radic Biol Med ; 113: 470-477, 2017 12.
Artigo em Inglês | MEDLINE | ID: mdl-29079525

RESUMO

During the phagocytosis of pathogens by phagocyte cells, the NADPH oxidase complex is activated to produce superoxide anion, a precursor of microbial oxidants. The activated NADPH oxidase complex from phagocytes consists in two transmembrane proteins (Nox2 and p22phox) and four cytosolic proteins (p40phox, p47phox, p67phox and Rac1-2). In the resting state of the cells, these proteins are dispersed in the cytosol, the membrane of granules and the plasma membrane. In order to synchronize the assembly of the cytosolic subunits on the membrane components of the oxidase, a fusion of the cytosolic proteins p47phox, p67phox and Rac1 named trimera was constructed. The trimera investigated in this paper is composed of the p47phox segment 1-286, the p67phox segment 1-212 and the mutated Rac1(Q61L). We demonstrate that the complex trimera-cyt b558 is functionally comparable to the one containing the separated subunits. Each of the subunits p47phox, p67phox and Rac1Q61L has kept its own activating property. The trimera is produced in an activated conformation as seen by circular dichroism. However, the presence of amphiphile is still necessary in a cell-free system to trigger superoxide anion production. The COS7gp91-p22 cells expressing the trimera produce continuously superoxide anion at high rate. This constitutive activity in cells can be of particular interest for understanding the NADPH oxidase functioning independently of signaling pathways.


Assuntos
Ácido Araquidônico/metabolismo , NADPH Oxidases/metabolismo , Fosfoproteínas/metabolismo , Subunidades Proteicas/metabolismo , Superóxidos/metabolismo , Proteínas rac1 de Ligação ao GTP/metabolismo , Animais , Células COS , Membrana Celular/química , Membrana Celular/metabolismo , Sistema Livre de Células , Chlorocebus aethiops , Expressão Gênica , Humanos , Cinética , NADP/metabolismo , NADPH Oxidases/genética , Neutrófilos/citologia , Neutrófilos/metabolismo , Fosfoproteínas/genética , Multimerização Proteica , Subunidades Proteicas/genética , Proteínas rac1 de Ligação ao GTP/genética
13.
J Phys Chem B ; 121(9): 2083-2094, 2017 03 09.
Artigo em Inglês | MEDLINE | ID: mdl-28194975

RESUMO

Gas-phase structural modifications induced by the oxidation of methionine of the two peptides of reverse sequence, methionine-valine (Met-Val) and valine-methionine (Val-Met), have been studied by mass-selected IR multiple photon dissociation (IRMPD) spectroscopy in the 800-2000 cm-1 fingerprint range at the Centre Laser Infrarouge d'Orsay free-electron laser facility. The oxidation has been achieved by •OH radicals generated by γ radiolysis. IRMPD spectra were interpreted by static and harmonic DFT calculations and Born-Oppenheimer molecular dynamics simulations, which are employed to take into account all anharmonic and finite-temperature effects. The diagnostic signature of the sulfoxide group in the final products of Met-Val and Val-Met oxidations, which is missing in the spectra of native peptides, has been recorded. Evidence has also been gathered that a mixture of R and S isomers of close energies is formed. An interconversion between different isomers has been unveiled in the case of the oxidized Met-Val dipeptide.


Assuntos
Dipeptídeos/química , Elétrons , Metionina/química , Simulação de Dinâmica Molecular , Teoria Quântica , Safrol/análogos & derivados , Enxofre/química , Sequência de Aminoácidos , Oxirredução , Fótons , Safrol/química , Espectrofotometria Infravermelho , Temperatura
14.
Biochim Biophys Acta Gen Subj ; 1861(1 Pt B): 3520-3530, 2017 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-27378459

RESUMO

BACKGROUND: Phagocytes kill ingested microbes by exposure to high concentrations of toxic reactive species generated by NADPH-oxidases. This membrane-bound electron-transferring enzyme is tightly regulated by cellular signaling cascades. So far, molecular and biophysical studies of the NADPH-oxidase were performed over limited temperature ranges, which weaken our understanding of immune response or inflammatory events. In this work, we have inspected the influence of temperature and lipid membrane properties on the NADPH-oxidase activity using a system free of cell complexity. METHODS: We have extended the experimental conditions of the accepted model for NADPH-oxidase activity, the so-called cell-free assay, to a large temperature range (10-40°C) using different membrane compositions (subcellular compartments or liposomes). RESULTS: A remarkable increase of superoxide production rate was observed with rising temperature. Synchrotron radiation circular dichroism data showed that this is not correlated with protein secondary structure changes. When lipid bilayers are in fluid phase, Arrhenius plots of the oxidase activity showed linear relationships with small activation energy (Ea), while when in solid phase, high Ea was found. The sterol content modulates kinetic and thermodynamic parameters. CONCLUSION: High temperature promotes the rate of superoxide production. The key element of this enhancement is related to membrane properties such as thickness and viscosity and not to protein structural changes. Membrane viscosity that can be driven by sterols is a paramount parameter of Ea of NADPH oxidase activity. The membrane bilayer state modulated by its sterol content may be considered locally as an enzyme regulator. This article is part of a Special Issue entitled "Science for Life" Guest Editor: Dr. Austen Angell, Dr. Salvatore Magazù and Dr. Federica Migliardo.


Assuntos
Membrana Celular/metabolismo , Fenômenos Químicos , NADPH Oxidases/metabolismo , Ácido Araquidônico/metabolismo , Dicroísmo Circular , Retículo Endoplasmático/metabolismo , Bicamadas Lipídicas/metabolismo , Modelos Biológicos , Pichia , Estabilidade Proteica , Proteolipídeos/metabolismo , Proteínas Recombinantes/metabolismo , Esteróis/metabolismo , Síncrotrons , Temperatura
15.
J Phys Chem B ; 120(37): 9875-86, 2016 09 22.
Artigo em Inglês | MEDLINE | ID: mdl-27564585

RESUMO

Oxidation of peptides or proteins by the OH(•) radicals produced by pulse radiolysis yields species identified by their absorption spectra in the UV-visible domain. However, the case of methionine (Met) in peptides is complex because its oxidation can lead to various free radicals with 2 center-3 electron (2c-3e) bonds. We have performed Monte Carlo/density functional theory molecular simulations of the radical cation of the methylated methionine aminoacid, Met(•+), taken as a model of the methonine residue of peptides, and of the radical cation of its van der Waals dimer, Met2(•+). The cation of the methionine residue displays a 2c-3e SN bond. The cation of dimer Met2(•+) displays three quasidegenerate conformers, one stabilized by a 2c-3e SS bond and the other two stabilized by ion-molecule interactions and made up of a neutral and a cationic unit. These conformers are characterized by their charge and spin density localization and their UV-visible absorption spectra. These spectra enable a discussion of the absorption spectra of the literature; in particular, we emphasize the role of dimers before and after the oxidation process.

16.
Biophys J ; 111(1): 69-78, 2016 Jul 12.
Artigo em Inglês | MEDLINE | ID: mdl-27410735

RESUMO

Using synchrotron radiation-based circular dichroism spectroscopy, we found that the DNA damage response induces an increase of α-helix structure and a decrease of ß-strand and turn structures in histone H2A-H2B extracted from x-irradiated human HeLa cells. The structural alterations correspond to the assumption that an average of eight amino acid residues form new α-helix structures at 310 K. We propose the structural transition from ß-strand and turn structures to an α-helix structure in H2A-H2B as a novel, to our knowledge, process involved in the DNA damage response.


Assuntos
Dano ao DNA , Histonas/química , Células HeLa , Histonas/metabolismo , Humanos , Conformação Proteica em alfa-Hélice , Conformação Proteica em Folha beta , Temperatura , Ubiquitinação
17.
FEBS J ; 283(15): 2896-910, 2016 08.
Artigo em Inglês | MEDLINE | ID: mdl-27284000

RESUMO

The NADPH oxidase is the sole enzymatic complex that produces, in a controlled way, superoxide anions. In phagocytes, it is constituted by the assembly of four cytosolic (p67(phox) , p47(phox) , p40(phox) and Rac) and two membrane (p22(phox) and Nox2) proteins. In response to pro-inflammatory mediators, the NADPH oxidase is activated. In cells, arachidonic acid (cis-AA), released by activated phospholipase A2, also plays a role in activation of the NADPH oxidase complex, but the mechanism of action of cis-AA is still a matter for debate. In cell-free systems, cis-AA is commonly used for activation. We have shown previously that trans-AA isomers were unable to activate the NADPH oxidase complex. Here, we aim to evaluate the structural changes in p47(phox) and p67(phox) induced by AA. The structural impact of both AA isomers on both cytosolic proteins was investigated by the accessibility of the thiol group and by circular dichroism in the far-UV for global folds. cis-AA induces secondary structure changes of p47(phox) and p67(phox) , while the trans isomer does not, suggesting that the changes observed are of importance for the activation process of these proteins. While five of the nine thiol groups in p67(phox) and all of them in p47(phox) have low access to the solvent when proteins are alone in solution, all of them become fully accessible when proteins are together. In conclusion, the secondary structures of p47(phox) and p67(phox) are both dependent on the presence of the partner protein in solution and on the presence of the activator molecule cis-AA.


Assuntos
Ácido Araquidônico/química , NADPH Oxidases/química , Fosfoproteínas/química , Compostos de Sulfidrila/química , Dicroísmo Circular , Humanos , NADPH Oxidases/genética , Estrutura Secundária de Proteína , Deleção de Sequência
18.
PLoS One ; 10(12): e0144829, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-26714308

RESUMO

Titanium dioxide (TiO2) anatase nanoparticles (NPs) are metal oxide NPs commercialized for several uses of everyday life. However their toxicity has been poorly investigated. Cellular internalization of NPs has been shown to activate macrophages and neutrophils that contribute to superoxide anion production by the NADPH oxidase complex. Transmission electron micrososcopy images showed that the membrane fractions were close to the NPs while fluorescence indicated an interaction between NPs and cytosolic proteins. Using a cell-free system, we have investigated the influence of TiO2 NPs on the behavior of the NADPH oxidase. In the absence of the classical activator molecules of the enzyme (arachidonic acid) but in the presence of TiO2 NPs, no production of superoxide ions could be detected indicating that TiO2 NPs were unable to activate by themselves the complex. However once the NADPH oxidase was activated (i.e., by arachidonic acid), the rate of superoxide anion production went up to 140% of its value without NPs, this effect being dependent on their concentration. In the presence of TiO2 nanoparticles, the NADPH oxidase produces more superoxide ions, hence induces higher oxidative stress. This hyper-activation and the subsequent increase in ROS production by TiO2 NPs could participate to the oxidative stress development.


Assuntos
NADPH Oxidases/metabolismo , Nanopartículas/toxicidade , Superóxidos/metabolismo , Titânio/química , Titânio/toxicidade , Animais , Bovinos , Humanos , Neutrófilos/citologia , Neutrófilos/efeitos dos fármacos , Neutrófilos/metabolismo , Estresse Oxidativo/efeitos dos fármacos , Tamanho da Partícula , Fatores de Tempo
19.
J Phys Chem B ; 119(23): 6885-93, 2015 Jun 11.
Artigo em Inglês | MEDLINE | ID: mdl-25951918

RESUMO

Recent experimental results about the oxidation of methionine enkephalin by ·OH radicals indicated an intramolecular electron transfer between the C-terminal methionine radical cation and the tyrosine N-terminus too fast to be observed. We have investigated the thermodynamic possibility of this intramolecular electron transfer by calculating the one-electron redox potentials of both residues for several conformations of the peptide, extracted from the experimental data of the Protein Data Bank (1PLW). Using a QM/MM approach, we show that the redox potential of the Met(•+)/Met couple is higher than that of the TyrOH(•+)/TyrOH one (tyrosine is denoted as TyrOH) for all conformations. The intramolecular electron transfer between both residues (from TyrOH to Met(•+)) is thus always thermodynamically allowed. Previously, we had performed topological studies on the intramolecular electron transfer which predicted this charge transfer. A study by cyclic voltammetry pointed out that the wave belonging to methionine is not present when methionine enkephalin is oxidized and only the direct involvement of the tyrosine residue is observed.


Assuntos
Encefalina Metionina/química , Cátions/química , Bases de Dados de Proteínas , Transporte de Elétrons , Elétrons , Concentração de Íons de Hidrogênio , Radical Hidroxila/química , Modelos Químicos , Estrutura Molecular , Oxirredução , Teoria Quântica , Termodinâmica
20.
Chemphyschem ; 16(3): 628-33, 2015 Feb 23.
Artigo em Inglês | MEDLINE | ID: mdl-25581220

RESUMO

The excited states of a set of popular sunscreen agents (2-hydroxybenzophenone, oxybenzone, and sulisobenzone) are studied by using femto- and nanosecond time-resolved spectroscopy. Upon excitation, the compounds undergo an ultrafast excited-state intramolecular proton transfer (ESIPT) reaction as the major energy-wasting process and the rate constant of this reaction is k=2×10(12) s(-1) . The ESIPT yields a keto conformer that undergoes a fast, picosecond internal conversion decay. However, a photodegradative pathway is a monophotonic HO bond breakage that subsequently leads to trace yields of phenoxyl radicals. Because potentially harmful phenoxyl radicals are formed upon irradiation of sunscreen agents, care should be taken about their reactivity towards biologically relevant compounds.


Assuntos
Benzofenonas/química , Protetores Solares/química , Cinética , Oxirredução , Fenóis/química , Fotólise , Espectrometria de Fluorescência , Raios Ultravioleta
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