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1.
Plant Physiol ; 174(2): 857-874, 2017 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-28385729

RESUMO

The cooperation of the mevalonate (MVA) and methylerythritol phosphate (MEP) pathways, operating in parallel in plants to generate isoprenoid precursors, has been studied extensively. Elucidation of the isoprenoid metabolic pathways is indispensable for the rational design of plant and microbial systems for the production of industrially valuable terpenoids. Here, we describe a new method, based on numerical modeling of mass spectra of metabolically labeled dolichols (Dols), designed to quantitatively follow the cooperation of MVA and MEP reprogrammed upon osmotic stress (sorbitol treatment) in Arabidopsis (Arabidopsis thaliana). The contribution of the MEP pathway increased significantly (reaching 100%) exclusively for the dominating Dols, while for long-chain Dols, the relative input of the MEP and MVA pathways remained unchanged, suggesting divergent sites of synthesis for dominating and long-chain Dols. The analysis of numerically modeled Dol mass spectra is a novel method to follow modulation of the concomitant activity of isoprenoid-generating pathways in plant cells; additionally, it suggests an exchange of isoprenoid intermediates between plastids and peroxisomes.


Assuntos
Arabidopsis/metabolismo , Dolicóis/química , Modelos Teóricos , Espectrometria de Massas por Ionização por Electrospray/métodos , Terpenos/metabolismo , Isótopos de Carbono , Cromatografia Gasosa/métodos , Dolicóis/metabolismo , Eritritol/análogos & derivados , Eritritol/metabolismo , Marcação por Isótopo/métodos , Redes e Vias Metabólicas , Ácido Mevalônico/análogos & derivados , Ácido Mevalônico/química , Ácido Mevalônico/metabolismo , Pressão Osmótica , Fitosteróis/biossíntese , Sorbitol/metabolismo , Fosfatos Açúcares/metabolismo , Xilulose/análogos & derivados , Xilulose/química
2.
BMC Vet Res ; 14(1): 328, 2018 Nov 06.
Artigo em Inglês | MEDLINE | ID: mdl-30400888

RESUMO

BACKGROUND: In this work, we report an electrochemical biosensor for the detection of anti-hemagglutinin antibodies against the swine virus H1N1 present in mice sera immunized with mixture of His6-H1 HA in monomeric and oligomeric form. The oriented immobilization of the recombinant His-tagged hemagglutinin (His6-H1 HA) consists of: (i) formation of a mixed layer of 4-mercaptobutanol (MBT) and the thiol derivative of dipyrromethene (DPM); (ii) complexation of Cu (II) by DPM; (iii) immobilization of His6-H1 HA via coordination bonds between Cu (II) sites from DPM-Cu (II) complex and imidazole nitrogen atoms of a histidine tag; (iv) filling free spaces with bovine serum albumin. The interactions between recombinant His6- H1 HA covalently attached to the electrode surface and the anti-hemagglutinin H1 antibodies present in mice sera were explored with Osteryoung square-wave voltammetry. RESULTS: This analytical device was able to detect the antibodies present in vaccinated mice sera diluted from 1 × 109 to 1 × 108 fold. CONCLUSIONS: The unprecedented sensitivity of described biosensor is much better than widely use ELISA test and other analytical methods for determination of antibodies against the influenza A viruses. It has been proved that redox active DPM-Cu (II) monolayer is a universal platform suitable for stable and oriented immobilization of any His-tagged sensing elements. Thus, this universal layer could be a base of numerous analytical devices suitable for detection of antibodies against different viruses.


Assuntos
Anticorpos Antivirais/imunologia , Glicoproteínas de Hemaglutininação de Vírus da Influenza/imunologia , Vírus da Influenza A Subtipo H1N1/imunologia , Vacinas contra Influenza/imunologia , Animais , Anticorpos Antivirais/sangue , Técnicas Biossensoriais , Feminino , Camundongos , Camundongos Endogâmicos BALB C , Infecções por Orthomyxoviridae/imunologia , Infecções por Orthomyxoviridae/veterinária , Oxirredução , Potenciometria/métodos , Suínos , Doenças dos Suínos/imunologia , Doenças dos Suínos/virologia
3.
Biochemistry ; 52(7): 1149-59, 2013 Feb 19.
Artigo em Inglês | MEDLINE | ID: mdl-23351007

RESUMO

S100 proteins play a crucial role in multiple important biological processes in vertebrate organisms acting predominantly as calcium signal transmitters. S100A1 is a typical representative of this family of proteins. After four Ca(2+) ions bind, it undergoes a dramatic conformational change, resulting in exposure, in each of its two identical subunits, a large hydrophobic cleft that binds to target proteins. It has been shown that abnormal expression of S100A1 is strongly correlated with a number of severe human diseases: cardiomyopathy and neurodegenerative disorders. A few years ago, we found that thionylation of Cys 85, the unique cysteine in two identical S100A1 subunits, leads to a drastic increase of the affinity of the protein for calcium. We postulated that the protein activated by thionylation becomes a more efficient calcium signal transmitter. Therefore, we decided to undertake, using nuclear magnetic resonance methods, a comparative study of the structure and dynamics of native and thionylated human S100A1 in its apo and holo states. In this paper, we present the results obtained for both forms of this protein in its holo state and compare them with the previously published structure of native apo-S100. The main conclusion that we draw from these results is that the increased calcium binding affinity of S100A1 upon thionylation arises, most probably, from rearrangement of the hydrophobic core in its apo form.


Assuntos
Cálcio/metabolismo , Proteínas S100/química , Proteínas S100/metabolismo , Cisteína/metabolismo , Humanos , Modelos Moleculares , Ressonância Magnética Nuclear Biomolecular , Conformação Proteica
4.
Rocz Panstw Zakl Hig ; 63(2): 171-8, 2012.
Artigo em Polonês | MEDLINE | ID: mdl-22928364

RESUMO

BACKGROUND: Taking into account the negative impact of stimulants, including alcohol, nicotine and excessive consumption of caffeine on the baby and his mother, a very important is to stop or to restrict their use, especially during pregnancy and lactation. OBJECTIVE: Purpose of the study was to evaluate alcohol consumption, cigarette smoking, tobacco smoke exposure and caffeine consumption in breastfeeding women from Masovian Province. MATERIAL AND METHOD: The survey was conducted from September 2010 till March 2011. The study group consisted of 102 breastfeeding women aged 19-38 years. Information on alcohol consumption, smoking and exposure to tobacco smoke was obtained by questionnaire interview. The results about caffeine intake were obtained using 3-day dietary records method and food frequency questionnaire method. Source of information about the caffeine content in products were the published literature, in the case of energy drinks the manufacturer's label. RESULTS: Among all women surveyed (n = 102), up 17% of respondents declared alcohol consumption, cigarette smoking of 6% and 15% of passive exposure to tobacco smoke. The average caffeine consumption in a group called "caffeine consumers" (n = 94) was 127.4 +/- 76.0 mg/person/day for 3-day dietary records method and 163.4 +/- 100.6 mg/person/day for the food frequency questionnaire method. The correlation coefficient between the used methods was r = 0.71 (p < 0.001). The main sources of caffeine, regardless of the method of data collection were: black tea, which provided about 60% of caffeine and ground coffee (about 20%) and instant coffee (about 13%). CONCLUSIONS: Despite general knowledge about the harmful effects of smoking cigarette/tobacco smoke exposure and the consumption of alcohol and foods high in caffeine, some respondents did not halt the use of these stimulants during lactation, indicating a need for an education in this field.


Assuntos
Consumo de Bebidas Alcoólicas/epidemiologia , Aleitamento Materno/estatística & dados numéricos , Cafeína/administração & dosagem , Estimulantes do Sistema Nervoso Central/administração & dosagem , Ingestão de Alimentos , Exposição Ambiental/estatística & dados numéricos , Fumar/epidemiologia , Adulto , Poluição do Ar em Ambientes Fechados/análise , Café , Comorbidade , Feminino , Humanos , Vigilância da População , Poluição por Fumaça de Tabaco/análise , Adulto Jovem
5.
Rocz Panstw Zakl Hig ; 63(3): 305-11, 2012.
Artigo em Polonês | MEDLINE | ID: mdl-23173335

RESUMO

BACKGROUND: Breastfeeding is considered the most beneficial, natural nutrition for babies. Qualitative and quantitative composition of breast milk is ideal for implementing all the nutritional needs of infants up to 6 months of age, assuming that the nursing mother's diet is correct. OBJECTIVE: The aim of the study was to evaluate the intake of energy, proteins, fat, carbohydrates and cholesterol in the group of 100 breastfeeding women, aged 19 to 38 years, from Masovian province. MATERIAL AND METHOD: The survey was conducted from September 2010 to March 2011. The results were obtained using a questionnaire survey and the 3-day dietary records method. RESULTS: Energy intake was compatible with the norms in 9% of women. As many as 91% of respondents characterized too high energy intake. Protein intake according to the norm was recorded in 64% of women, fat in 45% of respondents. Recommendations intake of polyunsaturated fatty acids was observed in 61% of group, saturated acids in 15% of women, carbohydrate in case of 36% of respondents. Cholesterol intake was too high at 45% of women. There was a statistically significant effect of education on intake of total fat and saturated fatty acids and polyunsaturated fats, sucrose and energy value. Women with higher education consumed 12% to 20% more of these nutrients compared to women with secondary education. CONCLUSIONS: There is need for further education of women during lactation on the importance of their properly balanced diet, as assessed food rations of lactating women have shown a lot of irregularities.


Assuntos
Aleitamento Materno/estatística & dados numéricos , Dieta/estatística & dados numéricos , Ingestão de Energia , Comportamento Alimentar , Estado Nutricional , Adulto , Carboidratos da Dieta/administração & dosagem , Gorduras na Dieta/administração & dosagem , Proteínas Alimentares/administração & dosagem , Feminino , Humanos , Recém-Nascido , Lactação , Micronutrientes/uso terapêutico , Necessidades Nutricionais , Polônia/epidemiologia , Saúde da Mulher , Adulto Jovem
6.
Chemistry ; 17(46): 12981-93, 2011 Nov 11.
Artigo em Inglês | MEDLINE | ID: mdl-21956694

RESUMO

A study concerning the effect of using a fluorinated aromatic solvent as the medium for olefin metathesis reactions catalysed by ruthenium complexes bearing N-heterocyclic carbene ligands is presented. The use of fluorinated aromatic hydrocarbons (FAH) as solvents for olefin metathesis reactions catalysed by standard commercially available ruthenium pre-catalysts allows substantially higher yields of the desired products to be obtained, especially in the case of demanding polyfunctional molecules, including natural and biologically active compounds. Interactions between the FAH and the second-generation ruthenium catalysts, which apparently improve the efficiency of the olefin metathesis transformation, have been studied by X-ray structure analysis and computations, as well as by carrying out a number of metathesis experiments. The optimisation of reaction conditions by using an FAH can be regarded as a complementary approach for the design of new improved ruthenium catalysts. Fluorinated aromatic solvents are an attractive alternative medium for promoting challenging olefin metathesis reactions.


Assuntos
Alcenos/química , Hidrocarbonetos Fluorados/química , Metano/análogos & derivados , Compostos Organometálicos/química , Rutênio/química , Catálise , Metano/química , Modelos Moleculares , Estrutura Molecular
7.
J Immunol Res ; 2019: 2463731, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-30729136

RESUMO

H1N1 influenza virus is still regarded as a serious pandemic threat. The most effective method of protection against influenza virus and the way to reduce the risk of epidemic or pandemic spread is vaccination. Influenza vaccine manufactured in a traditional way, though well developed, has some drawbacks and limitations which have stimulated interest in developing alternative approaches. In this study, we demonstrate that the recombinant H1 vaccine based on the hydrophilic haemagglutinin (HA) domain and produced in the yeast system elicited high titres of serum haemagglutination-inhibiting antibodies in mice. Transmission electron microscopy showed that H1 antigen oligomerizes into functional higher molecular forms similar to rosette-like structures. Analysis of the N-linked glycans using mass spectrometry revealed that the H1 protein is glycosylated at the same sites as the native HA. The recombinant antigen was secreted into a culture medium reaching approximately 10 mg/l. These results suggest that H1 produced in Pichia pastoris can be considered as the vaccine candidate against H1N1 virus.


Assuntos
Anticorpos Neutralizantes/sangue , Anticorpos Antivirais/sangue , Glicoproteínas de Hemaglutininação de Vírus da Influenza/imunologia , Vírus da Influenza A Subtipo H1N1/imunologia , Vacinas contra Influenza/imunologia , Animais , Antígenos Virais/imunologia , Feminino , Imunização , Vacinas contra Influenza/genética , Camundongos , Camundongos Endogâmicos BALB C , Infecções por Orthomyxoviridae/imunologia , Infecções por Orthomyxoviridae/prevenção & controle , Pichia/genética , Vacinas Sintéticas/genética , Vacinas Sintéticas/imunologia
8.
Antiviral Res ; 133: 242-9, 2016 09.
Artigo em Inglês | MEDLINE | ID: mdl-27498036

RESUMO

Highly pathogenic avian influenza is an on-going problem in poultry and a potential human pandemic threat. Pandemics occur suddenly and vaccine production must be fast and effective to be of value in controlling the spread of the virus. In this study we evaluated the potential of a recombinant protein from the extracellular domain of an H5 hemagglutinin protein produced in a yeast expression system to act as an effective vaccine. Protein production was efficient, with up to 200 mg purified from 1 L of culture medium. We showed that the deletion of the multibasic cleavage site from the protein improves oligomerization and, consequentially, its immunogenicity. We also showed that immunization with this deleted protein protected chickens from challenge with a highly pathogenic avian influenza H5N1 virus. Our results suggest that this recombinant protein produced in yeast may be an effective vaccine against H5N1 virus in poultry.


Assuntos
Antígenos Virais/imunologia , Galinhas , Virus da Influenza A Subtipo H5N1/imunologia , Vacinas contra Influenza/imunologia , Influenza Aviária/prevenção & controle , Domínios e Motivos de Interação entre Proteínas/imunologia , Vacinas de Partículas Semelhantes a Vírus/imunologia , Animais , Antígenos Virais/química , Antígenos Virais/isolamento & purificação , Glicoproteínas de Hemaglutininação de Vírus da Influenza/química , Glicoproteínas de Hemaglutininação de Vírus da Influenza/imunologia , Virus da Influenza A Subtipo H5N1/genética , Influenza Aviária/mortalidade , Influenza Aviária/virologia , Modelos Moleculares , Conformação Proteica , Multimerização Proteica , Proteínas Recombinantes/química , Proteínas Recombinantes/imunologia , Proteínas Recombinantes/isolamento & purificação , Proteínas Recombinantes/ultraestrutura , Vacinas de Partículas Semelhantes a Vírus/ultraestrutura
9.
Nat Commun ; 7: 12194, 2016 07 19.
Artigo em Inglês | MEDLINE | ID: mdl-27432510

RESUMO

Redox-regulated effector systems that counteract oxidative stress are essential for all forms of life. Here we uncover a new paradigm for sensing oxidative stress centred on the hydrophobic core of a sensor protein. RsrA is an archetypal zinc-binding anti-sigma factor that responds to disulfide stress in the cytoplasm of Actinobacteria. We show that RsrA utilizes its hydrophobic core to bind the sigma factor σ(R) preventing its association with RNA polymerase, and that zinc plays a central role in maintaining this high-affinity complex. Oxidation of RsrA is limited by the rate of zinc release, which weakens the RsrA-σ(R) complex by accelerating its dissociation. The subsequent trigger disulfide, formed between specific combinations of RsrA's three zinc-binding cysteines, precipitates structural collapse to a compact state where all σ(R)-binding residues are sequestered back into its hydrophobic core, releasing σ(R) to activate transcription of anti-oxidant genes.


Assuntos
Proteínas de Bactérias/química , Proteínas de Bactérias/metabolismo , Interações Hidrofóbicas e Hidrofílicas , Estresse Oxidativo , Fator sigma/antagonistas & inibidores , Sequência de Aminoácidos , Cisteína/metabolismo , Cinética , Espectroscopia de Ressonância Magnética , Oxirredução , Zinco/metabolismo
10.
FEBS Lett ; 587(24): 3928-34, 2013 Dec 11.
Artigo em Inglês | MEDLINE | ID: mdl-24211447

RESUMO

Initiation is the rate-limiting step during mRNA 5' cap-dependent translation, and thus a target of a strict control in the eukaryotic cell. It is shown here by analytical ultracentrifugation and fluorescence spectroscopy that the affinity of the human translation inhibitor, eIF4E-binding protein (4E-BP1), to the translation initiation factor 4E is significantly higher when eIF4E is bound to the cap. The 4E-BP1 binding stabilizes the active eIF4E conformation and, on the other hand, can facilitate dissociation of eIF4E from the cap. These findings reveal the particular allosteric effects forming a thermodynamic cycle for the cooperative regulation of the translation initiation inhibition.


Assuntos
Proteínas Adaptadoras de Transdução de Sinal/metabolismo , Fator de Iniciação 4E em Eucariotos/metabolismo , Iniciação Traducional da Cadeia Peptídica/fisiologia , Fosfoproteínas/metabolismo , Multimerização Proteica/fisiologia , Capuzes de RNA/metabolismo , Proteínas Adaptadoras de Transdução de Sinal/química , Proteínas de Ciclo Celular , Fator de Iniciação 4E em Eucariotos/química , Fatores de Iniciação em Eucariotos/química , Fatores de Iniciação em Eucariotos/metabolismo , Fracionamento por Campo e Fluxo , Humanos , Modelos Biológicos , Complexos Multiproteicos/química , Complexos Multiproteicos/metabolismo , Fosfoproteínas/química , Ligação Proteica/fisiologia , Conformação Proteica , RNA Mensageiro/química , RNA Mensageiro/metabolismo , Ultracentrifugação
11.
Biochemistry ; 45(27): 8294-300, 2006 Jul 11.
Artigo em Inglês | MEDLINE | ID: mdl-16819828

RESUMO

ZAS proteins are widespread bacterial zinc-containing anti-sigma factors that regulate the activity of sigma factors in response to diverse cues. One of the best characterized ZAS proteins is RsrA from Streptomyces coelicolor, which responds to disulfide stress. Zn-RsrA binds and represses the transcriptional activity of sigmaR in the reducing environment of the cytoplasm but undergoes reversible, intramolecular disulfide bond formation during oxidative stress. This expels the single metal ion and causes dramatic structural changes in RsrA that result in its dissociation from sigmaR, leaving the sigma factor free to activate the transcription of antioxidant genes. We showed recently that Zn2+ serves a critical role in modulating the redox activity of RsrA thiols but uncertainty remains as to how the metal ion is coordinated in RsrA and related ZAS proteins. Using a combination of random and site-specific mutagenesis with zinc K-edge extended X-ray absorption fine structure (EXAFS) spectroscopy, we have assigned unambiguously the metal ligands in RsrA, thereby distinguishing between the different ligation models that have been proposed. The data show that the zinc site in RsrA is comprised of Cys11, His37, Cys41, and Cys44. Three of these residues are part of a conserved ZAS-specific sequence motif (H37xxxC41xxC44), with the fourth ligand, Cys11, found in a subset of ZAS proteins. Cys11 and Cys44 form the trigger disulfide in RsrA, explaining why the metal ion is expelled during oxidation. We discuss these data in the context of redox sensing by RsrA and the sensory mechanisms of other ZAS proteins.


Assuntos
Proteínas de Bactérias/química , Fatores de Transcrição/química , Zinco/química , Motivos de Aminoácidos , Sequência de Aminoácidos , Proteínas de Bactérias/genética , Sítios de Ligação/genética , Sequência Conservada , Cisteína/química , Cisteína/genética , Histidina/química , Histidina/genética , Ligantes , Dados de Sequência Molecular , Oxirredução , Fatores de Transcrição/genética
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