RESUMEN
We report on the first Belle search for a light CP-odd Higgs boson, A^{0}, that decays into low mass dark matter, χ, in final states with a single photon and missing energy. We search for events produced via the dipion transition Ï(2S)âÏ(1S)π^{+}π^{-}, followed by the on-shell process Ï(1S)âγA^{0} with A^{0}âχχ, or by the off-shell process Ï(1S)âγχχ. Utilizing a data sample of 157.3×10^{6} Ï(2S) decays, we find no evidence for a signal. We set limits on the branching fractions of such processes in the mass ranges M_{A^{0}}<8.97 GeV/c^{2} and M_{χ}<4.44 GeV/c^{2}. We then use the limits on the off-shell process to set competitive limits on WIMP-nucleon scattering in the WIMP mass range below 5 GeV/c^{2}.
RESUMEN
We report the first observation of the double strange baryon Ξ(1620)^{0} in its decay to Ξ^{-}π^{+} via Ξ_{c}^{+}âΞ^{-}π^{+}π^{+} decays based on a 980 fb^{-1} data sample collected with the Belle detector at the KEKB asymmetric-energy e^{+}e^{-} collider. The mass and width are measured to be 1610.4±6.0(stat)_{-4.2}^{+6.1} (syst) MeV/c^{2} and 59.9±4.8(stat)_{-7.1}^{+2.8}(syst) MeV, respectively. We obtain 4.0σ evidence of the Ξ(1690)^{0} with the same data sample. These results shed light on the structure of hyperon resonances with strangeness S=-2.
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We report the first observation of the hadronic transition Ï(4S)âη^{'}Ï(1S), using 496 fb^{-1} data collected at the Ï(4S) resonance with the Belle detector at the KEKB asymmetric-energy e^{+}e^{-} collider. We reconstruct the η^{'} meson through its decays to ρ^{0}γ and to π^{+}π^{-}η, with ηâγγ. We measure B(Ï(4S)âη^{'}Ï(1S))=[3.43±0.88(stat)±0.21(syst)]×10^{-5}, with a significance of 5.7σ.
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Newborn screening (NBS) for Krabbe disease, a rare neurodegenerative disorder caused by deficient galactocerebrosidase (GALC) enzyme activity, has recently been implemented in a number of US states. However, the spectrum of phenotypic manifestations associated with deficient GALC activity complicates the management of screen-positive newborns and underscores the need to identify clinically relevant biomarkers. Earlier studies with a small number of patients identified psychosine, a substrate of the GALC enzyme, as a potential biomarker for Krabbe disease. In this study, we provide, for the first time, longitudinal data on dried blood spot (DBS) psychosine concentrations in different Krabbe disease phenotypes for both untreated patients and those treated with hematopoietic stem cell transplantation (HSCT). Our cohort included patients previously identified by NBS to be at high risk to develop Krabbe disease. Substantially elevated DBS psychosine concentration during the newborn period was found to be a highly specific marker for infantile Krabbe disease. This finding supports the use of DBS psychosine concentration as a second-tier NBS test to aid in the identification of patients who require urgent evaluation for HSCT. In addition, longitudinal assessments showed that both natural disease progression and treatment with HSCT were associated with decreases in DBS psychosine concentrations. Based on these findings we provide recommendations for the interpretation of psychosine concentrations in DBS specimens collected during the first year of life. Future studies should aim to better delineate the relationship between DBS psychosine concentration and disease onset in patients with later-onset forms of Krabbe disease.
Asunto(s)
Biomarcadores/sangre , Leucodistrofia de Células Globoides/diagnóstico , Psicosina/sangre , Adolescente , Niño , Preescolar , Progresión de la Enfermedad , Pruebas con Sangre Seca , Humanos , Lactante , Recién Nacido , Leucodistrofia de Células Globoides/tratamiento farmacológico , Tamizaje Neonatal , Fenotipo , Espectrometría de Masas en TándemRESUMEN
We report the first evidence for isospin violation in BâK^{*}γ and the first measurement of the difference of CP asymmetries between B^{+}âK^{*+}γ and B^{0}âK^{*0}γ. This analysis is based on the data sample containing 772×10^{6}BB[over ¯] pairs that was collected with the Belle detector at the KEKB energy-asymmetric e^{+}e^{-} collider. We find evidence for the isospin violation with a significance of 3.1σ, Δ_{0+}=[+6.2±1.5(stat)±0.6(syst)±1.2(f_{+-}/f_{00})]%, where the third uncertainty is due to the uncertainty on the fraction of B^{+}B^{-} to B^{0}B[over ¯]^{0} production in Ï(4S) decays. The measured value is consistent with predictions of the standard model. The result for the difference of CP asymmetries is ΔA_{CP}=[+2.4±2.8(stat)±0.5(syst)]%, consistent with zero. The measured branching fractions and CP asymmetries for charged and neutral B meson decays are the most precise to date. We also calculate the ratio of branching fractions of B^{0}âK^{*0}γ to B_{s}^{0}âÏγ.
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Background Secreted phospholipase A(2) (sPLA(2) ) may be important mediators of asthma, but the specific sPLA(2) s involved in asthma are not known. Objective To evaluate sPLA(2) group IIA, V, and X proteins (sPLA(2) -IIA, sPLA(2) -V, and sPLA(2) -X) in bronchoalveolar lavage (BAL) fluid, BAL cells, and airway epithelial cells of subjects with and without asthma, and examine the relationship between the levels of specific sPLA(2) enzymes and airway inflammation, asthma severity, and lung function. Methods The expression of sPLA(2) -IIA, sPLA(2) -V, and sPLA(2) -X in BAL cells and epithelial brushings was assessed by qPCR. The levels of these sPLA(2) proteins and sPLA(2) activity with and without group II and group X-specific inhibitors were measured in BAL fluid from 18 controls and 39 asthmatics. Results The airway epithelium expressed sPLA(2) -X at higher levels than either sPLA(2) -IIA or sPLA(2) -V, whereas BAL cells expressed sPLA(2) -IIA and sPLA(2) -X at similar levels. The majority of sPLA(2) activity in BAL fluid was attributed to either sPLA(2) -IIA or sPLA(2) -X. After 10-fold concentration of BAL fluid, the levels of sPLA(2) -X normalized to total protein were increased in asthma and were associated with lung function, the concentration of induced sputum neutrophils, and prostaglandin E(2) . The levels of sPLA(2) -IIA were elevated in asthma when normalized to total protein, but were not related to lung function, markers of airway inflammation or eicosanoid formation. Conclusions and Clinical Relevance These data indicate that sPLA(2) -IIA and sPLA(2) -X are the major sPLA(2) s in human airways, and suggest a link between the levels of sPLA(2) -X in the airways and several features of asthma.
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Asma/enzimología , Fosfolipasas A2 Grupo II/metabolismo , Fosfolipasas A2 Grupo X/metabolismo , Sistema Respiratorio/enzimología , Adulto , Asma/inmunología , Líquido del Lavado Bronquioalveolar/citología , Líquido del Lavado Bronquioalveolar/inmunología , Activación Enzimática/inmunología , Femenino , Regulación Enzimológica de la Expresión Génica/inmunología , Humanos , Masculino , Persona de Mediana Edad , Mucosa Respiratoria/metabolismo , Sistema Respiratorio/inmunología , Infecciones del Sistema Respiratorio/enzimología , Infecciones del Sistema Respiratorio/inmunologíaRESUMEN
AirwayCentric approach to prevention of dentofacial disorders. The correct development of functions is important for the prevention of dentofacial disorders from the first days of life. The first and foremost function, to which all others are adapting, is nasal breathing. The AirwayCentric® method focuses on nasal breathing during early development and throughout childhood to promote: Neurobehavioural development and the brain, development of the craniofacial and respiratory complex, correct dental occlusion, proper and restful sleep and to improve performance and life overall. By working at the same time on orofacial functions and structures, many dentofacial disorders can be prevented.
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Terapia Miofuncional , Niño , HumanosRESUMEN
Previous studies have shown that animal cells contain isoprenoid-modified proteins and that one of these proteins, lamin B, contains a thioether-linked farnesyl group that is attached to cysteine. In the present study, a novel isoprenoid-modification was identified by labeling HeLa cells with [3H]mevalonic acid and analyzing proteolytic digests of the total cell protein. Radioactive fragments were purified from these digests and treated with Raney nickel. The released, labeled material was analyzed by gas-liquid chromatography (GC) and mass spectrometry (MS). This approach revealed that an all-trans geranylgeranyl group was a major isoprenoid modification.
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Diterpenos/metabolismo , Proteínas/metabolismo , Cromatografía en Gel , Cromatografía por Intercambio Iónico , Cromatografía de Gases y Espectrometría de Masas , Células HeLa/metabolismo , Humanos , Ácido Mevalónico/metabolismo , Estructura Molecular , Níquel , Fragmentos de PéptidosRESUMEN
The crystal structure of a complex between a phosphonate transition-state analogue and the phospholipase A2 (PLA2) from Naja naja atra venom has been solved and refined to a resolution of 2.0 angstroms. The identical stereochemistry of the two complexes that comprise the crystal's asymmetric unit indicates both the manner in which the transition state is stabilized and how the hydrophobic fatty acyl chains of the substrate are accommodated by the enzyme during interfacial catalysis. The critical features that suggest the chemistry of binding and catalysis are the same as those seen in the crystal structure of a similar complex formed with the evolutionarily distant bee-venom PLA2.
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Venenos Elapídicos/análisis , Fosfatidiletanolaminas/metabolismo , Fosfolipasas A/química , Secuencia de Aminoácidos , Venenos de Abeja/análisis , Sitios de Unión , Calcio/metabolismo , Catálisis , Fenómenos Químicos , Química Física , Cristalización , Enlace de Hidrógeno , Datos de Secuencia Molecular , Estructura Molecular , Fosfolipasas A/metabolismo , Fosfolipasas A2 , Conformación ProteicaRESUMEN
The 2.0 angstroms crystal structure of a complex containing bee-venom phospholipase A2 (PLA2) and a phosphonate transition-state analogue was solved by multiple isomorphous replacement. The electron-density map is sufficiently detailed to visualize the proximal sugars of the enzyme's N-linked carbohydrate and a single molecule of the transition-state analogue bound ot its active center. Although bee-venom PLA2 does not belong to the large homologous Class I/II family that encompasses most other well-studied PLA2s, there is segmental sequence similarity and conservation of many functional substructures. Comparison of the bee-venom enzyme with other phospholipase structures provides compelling evidence for a common catalytic mechanism.
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Venenos de Abeja/análisis , Fosfatidiletanolaminas/metabolismo , Fosfolipasas A/química , Secuencia de Aminoácidos , Sitios de Unión , Calcio/metabolismo , Metabolismo de los Hidratos de Carbono , Catálisis , Fenómenos Químicos , Química Física , Cristalización , Enlace de Hidrógeno , Datos de Secuencia Molecular , Estructura Molecular , Fosfolipasas A/metabolismo , Fosfolipasas A2 , Conformación ProteicaRESUMEN
Phospholipase A2 (PLA2) participates in a wide range of cellular processes including inflammation and transmembrane signaling. A human nonpancreatic secretory PLA2 (hnps-PLA2) has been identified that is found in high concentrations in the synovial fluid of patients with rheumatoid arthritis and in the plasma of patients with septic shock. This enzyme is secreted from certain cell types in response to the proinflammatory cytokines, tumor necrosis factor or interleukin-1. The crystal structures of the calcium-bound form of this enzyme have been determined at physiological pH both in the presence [2.1 angstrom (A) resolution] and absence (2.2 A resolution) of a transition-state analogue. Although the critical features that suggest the chemistry of catalysis are identical to those inferred from the crystal structures of other extracellular PLA2s, the shape of the hydrophobic channel of hnps-PLA2 is uniquely modulated by substrate binding.
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Inflamación/enzimología , Fosfolipasas A/ultraestructura , Secuencia de Aminoácidos , Sitios de Unión , Calcio/química , Gráficos por Computador , Cristalografía , Espacio Extracelular/enzimología , Humanos , Datos de Secuencia Molecular , Fosfolipasas A/antagonistas & inhibidores , Fosfolipasas A2 , Conformación Proteica , Proteínas Recombinantes , Alineación de Secuencia , Difracción de Rayos XRESUMEN
A method involving electron paramagnetic resonance spectroscopy of a site-selectively spin-labeled peripheral membrane protein in the presence and absence of membranes and of a water-soluble spin relaxant (chromium oxalate) has been developed to determine how bee venom phospholipase A2 sits on the membrane. Theory based on the Poisson-Boltzmann equation shows that the rate of spin relaxation of a protein-bound nitroxide by a membrane-impermeant spin relaxant depends on the distance (up to tens of angstroms) from the spin probe to the membrane. The measurements define the interfacial binding surface of this secreted phospholipase A2.
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Glicerofosfolípidos , Proteínas de la Membrana/química , Membranas Artificiales , Fosfolipasas A/química , Venenos de Abeja/química , Sitios de Unión , Cromatos , Espectroscopía de Resonancia por Spin del Electrón , Liposomas , Proteínas de la Membrana/análisis , Proteínas de la Membrana/genética , Proteínas de la Membrana/metabolismo , Modelos Moleculares , Mutación , Oxalatos , Ácidos Fosfatidicos , Fosfolipasas A/análisis , Fosfolipasas A/genética , Fosfolipasas A/metabolismo , Fosfolipasas A2 , Marcadores de Spin , Propiedades de SuperficieRESUMEN
A chemical description of the action of phospholipase A2 (PLA2) can now be inferred with confidence from three high-resolution x-ray crystal structures. The first is the structure of the PLA2 from the venom of the Chinese cobra (Naja naja atra) in a complex with a phosphonate transition-state analogue. This enzyme is typical of a large, well-studied homologous family of PLA2S. The second is a similar complex with the evolutionarily distant bee-venom PLA2. The third structure is the uninhibited PLA2 from Chinese cobra venom. Despite the different molecular architectures of the cobra and bee-venom PLA2s, the transition-state analogue interacts in a nearly identical way with the catalytic machinery of both enzymes. The disposition of the fatty-acid side chains suggests a common access route of the substrate from its position in the lipid aggregate to its productive interaction with the active site. Comparison of the cobra-venom complex with the uninhibited enzyme indicates that optimal binding and catalysis at the lipid-water interface is due to facilitated substrate diffusion from the interfacial binding surface to the catalytic site rather than an allosteric change in the enzyme's structure. However, a second bound calcium ion changes its position upon the binding of the transition-state analogue, suggesting a mechanism for augmenting the critical electrophile.
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Fosfolipasas A/metabolismo , Venenos de Abeja/análisis , Sitios de Unión , Calcio/metabolismo , Catálisis , Fenómenos Químicos , Química Física , Venenos Elapídicos/análisis , Modelos Moleculares , Estructura Molecular , Organofosfonatos/metabolismo , Fosfolipasas A/química , Fosfolipasas A2 , Fosfolípidos/metabolismo , Conformación Proteica , Difracción de Rayos XRESUMEN
Recent studies have indicated that eukaryotic cells contain proteins that are post-translationally modified by long-chain, thioether-linked prenyl groups. These proteins include yeast mating factors, ras proteins and nuclear lamins. The modification occurs on a cysteine residue near the C terminus and appears to initiate a set of additional protein modification reactions that promote attachment of the proteins to specific membranes.
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Membrana Celular/metabolismo , Células/metabolismo , Células Eucariotas/metabolismo , Fosfatos de Poliisoprenilo/metabolismo , Proteínas/metabolismo , Animales , Humanos , Laminas , Factor de Apareamiento , Proteínas Nucleares/metabolismo , Péptidos/metabolismo , Procesamiento Proteico-Postraduccional , Proteínas Proto-Oncogénicas/metabolismo , Proteínas Proto-Oncogénicas p21(ras)RESUMEN
We have shown previously that interleukin 1 (IL-1) stimulates eicosanoid production in glomerular mesangial cells (MC) by de novo synthesis of a 14-kD, group II phospholipase A2 (PLA2). IL-1-stimulated prostaglandin E2 synthesis precedes expression of this enzyme, suggesting that another PLA2 isoform must be more rapidly activated. In the presence but not absence of calcium inophore, [3H]arachidonate release is increased significantly as early as 5 min after addition of IL-1, and IL-1 concurrently stimulates a Ca(2+)-dependent phospholipase activity, which was characterized as the cytosolic form of PLA2 (cPLA2). IL-1 does not alter either cPLA2 mRNA expression or mass in serum-stimulated MC, suggesting that cPLA2 activity is increased by a posttranslational modification. IL-1 treatment for 30 min doubles 32P incorporation into immunoprecipitable cPLA2 protein, concordant with the increase in enzyme activity. Immunoblot analysis of extracts derived from IL-1-treated (30 min) cells demonstrates a decreased mobility of cPLA2, and treatment of MC lysates with acid phosphatase significantly reduces cytokine-activated cPLA2 activity, further indicating that IL-1 stimulates phosphorylation of the enzyme. IL-1 treatment (24 h) of serum-deprived MC doubled cPLA2 mRNA, protein, and activity. In summary, IL-1 increases cPLA2 activity in a biphasic, time-dependent manner both by posttranslational modification and de novo synthesis. We consider cPLA2 activation a key step in IL-1-stimulated synthesis of pro-inflammatory, lipid mediators, and an integral event in the phenotypic responses induced in target cells by this cytokine.
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Mesangio Glomerular/metabolismo , Interleucina-1/farmacología , Fosfolipasas A/metabolismo , Animales , Ácido Araquidónico/metabolismo , Citosol/enzimología , Activación Enzimática/efectos de los fármacos , Fosfolipasas A/genética , Fosfolipasas A2 , Fosforilación , ARN Mensajero/análisis , RatasRESUMEN
Secreted phospholipases A(2) have similar catalytic sites, but vastly different interfacial binding surfaces that modulate their binding affinity for different kinds of phospholipid vesicles by several orders of magnitude. The structure/function principles that dictate both the differential interfacial binding and the physiological function of these enzymes are beginning to be unraveled.
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Membrana Celular/metabolismo , Fosfolipasas A/metabolismo , Animales , Venenos de Abeja/enzimología , Sitios de Unión , Calcio/fisiología , Catálisis , Bovinos , Cristalografía por Rayos X , Eicosanoides/metabolismo , Venenos Elapídicos/enzimología , Humanos , Liposomas/metabolismo , Lípidos de la Membrana/metabolismo , Modelos Moleculares , Mutagénesis Sitio-Dirigida , Fosfolipasas A/química , Fosfolipasas A/genética , Fosfolípidos/metabolismo , Unión Proteica , Conformación Proteica , Electricidad Estática , Porcinos , Triptófano/fisiologíaRESUMEN
We describe an approach for the accurate quantification and concurrent sequence identification of the individual proteins within complex mixtures. The method is based on a class of new chemical reagents termed isotope-coded affinity tags (ICATs) and tandem mass spectrometry. Using this strategy, we compared protein expression in the yeast Saccharomyces cerevisiae, using either ethanol or galactose as a carbon source. The measured differences in protein expression correlated with known yeast metabolic function under glucose-repressed conditions. The method is redundant if multiple cysteinyl residues are present, and the relative quantification is highly accurate because it is based on stable isotope dilution techniques. The ICAT approach should provide a widely applicable means to compare quantitatively global protein expression in cells and tissues.
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Marcadores de Afinidad , Marcaje Isotópico , Proteínas/química , Secuencia de Aminoácidos , Cromatografía Liquida , Espectrometría de MasasRESUMEN
A family of 14-20kDa, disulfide-rich, calcium-dependent secreted phospholipases A2 (sPLA2s) that release fatty acids from the sn-2 position of glycerophospholipids can be found in mammals. They have a diverse array of tissue distribution and biological functions. In this chapter we provide detailed protocols for production of nearly all of the mouse and human sPLA2s mainly by expression in bacteria and in vitro refolding or by expression in insect cells. High-resolution mass spectrometry and enzymatic assays were, respectively, used to show that all disulfides are formed and that the enzymes are active, strongly suggesting that each sPLA2 was prepared in the structurally native form. The availability of these proteins has allowed kinetic studies to be carried out, to prepare highly selective antisera, to screen for selective inhibitors, to study receptor binding, and to study the action of each enzyme on mammalian cell membranes and their in vivo biological roles.
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Expresión Génica , Fosfolipasas A2 Secretoras/metabolismo , Fosfolípidos/metabolismo , Proteínas Recombinantes de Fusión/metabolismo , Animales , Baculoviridae/genética , Baculoviridae/metabolismo , Clonación Molecular , Disulfuros/química , Pruebas de Enzimas , Escherichia coli/genética , Escherichia coli/metabolismo , Factor Xa/química , Glutatión Transferasa/genética , Glutatión Transferasa/metabolismo , Células HEK293 , Humanos , Hidrólisis , Cuerpos de Inclusión/química , Isoenzimas/genética , Isoenzimas/metabolismo , Cinética , Ratones , Fosfolipasas A2 Secretoras/química , Fosfolipasas A2 Secretoras/genética , Fosfolípidos/química , Replegamiento Proteico , Proteínas Recombinantes de Fusión/química , Proteínas Recombinantes de Fusión/genética , Células Sf9 , Spodoptera , Distribución TisularRESUMEN
The iron transport protein, transferrin, binds two metal ions and, concomitantly, two carboxylate anions. The metal ion indicators, xylenol orange and semi-xylenol orange are carboxylate anions which exhibit a characteristic visible spectrum when attached to a metal. We prepared the ternary complexes VO2+-transferrin-xylenol orange and VO2+-transferrin-semi-xylenol orange. The EPR spectra show that the vanadyl ion is attached to the protein and the visible spectra show that the xylenol orange or semi-xylenol orange is attached to the metal. The implication is that in other metal-transferrin-anion complexes, the anion is directly attached to the metal.
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Glicina/análogos & derivados , Transferrina , Xilenos , Fenómenos Químicos , Química , Espectroscopía de Resonancia Magnética , Fenoles , Sulfóxidos , VanadioRESUMEN
A growing number of amphiphiles are known to form high axial ratio microstructures (HARMs) such as the hollow cylindrical microstructures called lipid tubules. As a prelude to exploring the potential of HARMs formed from lipopeptides in controlled release drug delivery, several microstructure formation conditions were investigated. We report the preparation of several glutamic acid dialkyl amides with varying alkyl chain lengths bearing a verity of peptides (1-4 amino acids) [peptide-Glu-(NHCnH2n+1)2, n=12, 14, 16]. These surfactants have been rapidly and efficiently converted into HARMs in aqueous buffer at physiological pH and ionic strength, or in buffer containing MeOH or EtOH. Helical ribbons and tubular HARMs were produced that were stable for as long as 6 months below the phase transition temperatures of the compounds. To estimate the stability of HARMs in vivo, HARMs formed from (Pro)3-Glu(NHC16H33)2 were incubated with DOPC liposomes or fetal calf serum at 40 degreesC. HARM size and shape did not change significantly, suggesting that such lipopeptide particles can retain their morphology long enough in vivo to be useful as drug delivery vehicles.