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Artykuły w czasopismach na temat "Binding phases"
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Lee-Schoenfeld, Vera. "Binding, Phases, and Locality". Syntax 11, nr 3 (grudzień 2008): 281–98. http://dx.doi.org/10.1111/j.1467-9612.2008.00118.x.
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Molina, D., E. Lomba i G. Kahl. "Tight-binding model of selenium disordered phases". Physical Review B 60, nr 9 (1.09.1999): 6372–82. http://dx.doi.org/10.1103/physrevb.60.6372.
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Harris, A. B., T. C. Lubensky i E. J. Mele. "Flux phases in two-dimensional tight-binding models". Physical Review B 40, nr 4 (1.08.1989): 2631–34. http://dx.doi.org/10.1103/physrevb.40.2631.
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Pöppl, Álan G., Sandra C. Valle, Félix H. D. González, Luiz C. Kucharski i Roselis S. M. da Silva. "Insulin binding characteristics in canine muscle tissue: effects of the estrous cycle phases". Pesquisa Veterinária Brasileira 36, nr 8 (sierpień 2016): 761–66. http://dx.doi.org/10.1590/s0100-736x2016000800014.
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Abstract: Hormonal fluctuations during the different estrous cycle are a well-recognized cause of insulin resistance in bitches, and little is known about insulin receptor binding or post-binding defects associated with insulin resistance in dogs. To evaluate insulin binding characteristics in muscle tissue of bitches during the estrous cycle, 17 owned bitches were used in the study (six in anestrus, five in estrus, and six in diestrus). An intravenous glucose tolerance test (IVGTT) was performed in all patients by means of injection of 1mL/kg of a glucose 50% solution (500mg/kg), with blood sample collection for glucose determination at 0, 3, 5, 7, 15, 30, 45 and 60 minutes after glucose infusion. Muscle samples, taken after spaying surgery, were immediately frozen in liquid nitrogen and then stored at -80 ºC until the membranes were prepared by sequential centrifugation after being homogenized. For binding studies, membranes were incubated in the presence of 20,000cpm of human 125I-insulin and in increasing concentrations of unlabeled human regular insulin for cold saturation. The IVGTT showed no differences among bitches during the estrous cycle regarding baseline glycemia or glycemic response after glucose infusion. Two insulin binding sites - high-affinity and low-affinity ones - were detected by Scatchard analysis, and significant statistical differences were observed in the dissociation constant (Kd1) and maximum binding capacity (Bmax1) of the high-affinity binding sites. The Kd1 for the anestrus group (6.54±2.77nM/mg of protein) was smaller (P<0.001) than for the estrus (28.54±6.94nM/mg of protein) and diestrus (15.56±3.88nM/mg of protein) groups. Bmax1 in the estrus (0.83±0.42nM/mg of protein) and diestrus (1.24±0.24nM/mg of protein) groups were also higher (P<0.001) than the values observed in anestrus (0.35±0.06nM/mg of protein). These results indicate modulation of insulin binding characteristics during different phases of the estrous cycle in dogs, showing that muscle insulin binding affinity for its receptor is reduced during estrus and diestrus. However, this poor hormone-receptor affinity is compensated for by a greater total binding capacity, once there is no difference in patients' glycemic response after an intravenous glucose load.
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DUFOUR, J. J., X. J. C. DUFOUR i J. D. VINKO. "PICO-CHEMISTRY: THE POSSIBILITY OF NEW PHASES IN SOME HYDROGEN/METAL SYSTEMS". International Journal of Modern Physics B 27, nr 15 (4.06.2013): 1362038. http://dx.doi.org/10.1142/s0217979213620385.
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In the standard model, matter is an assembly of quarks that combine under the action of the strong nuclear force to give nucleons (protons and neutrons), further giving atom nuclei that under the action of the electromagnetic force combine with electrons to render atoms and molecules. Each of these interactions has a well defined range of binding energies. A novel type of purely electromagnetic interaction is proposed, with binding energies and dimensions between chemistry and nuclear. This type of binding could result in completely novel materials (super-conductivity) and potential energy production.
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Patterson, Kristine B., Julie B. Dumond, Heather A. Prince, Amanda J. Jenkins, Kimberly K. Scarsi, Ruili Wang, Stephanie Malone, Michael G. Hudgens i Angela D. M. Kashuba. "Protein Binding of Lopinavir and Ritonavir During 4 Phases of Pregnancy". JAIDS Journal of Acquired Immune Deficiency Syndromes 63, nr 1 (maj 2013): 51–58. http://dx.doi.org/10.1097/qai.0b013e31827fd47e.
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SAARELA, MIKKO, i TAUNO TAIPALEENMÄKI. "QUANTUM FLUID MIXTURES IN DIFFERENT PHASES". International Journal of Modern Physics B 17, nr 28 (10.11.2003): 5227–42. http://dx.doi.org/10.1142/s0217979203020375.
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Variational theory of quantum fluid mixtures is presented with the emphasis on the stability and phase transitions. We give results on two systems where new interesting phases are predicted. Dilute mixtures of 3 He impurities in the liquid 4 He in two dimensions form loosely bound pairs, dimers. The binding energy of the dimer ranges from milli- to micro-Kelvins with increasing 4 He density. The dimerised mixture of 3 He atoms is stable up to maximum solubility of ≈3%. Electrons and holes in semiconductors form a homogeneous mixture, electron-hole liquid. We predict that at low densities this system becomes unstable against clustering of charges and a liquid phase with a mixture of bound charged clusters could be formed.
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SLIWKO, V. L., P. BLAHA, P. MOHN i K. SCHWARZ. "MAGNETIC PHASES OF BODY CENTERED CUBIC MANGANESE". International Journal of Modern Physics B 07, nr 01n03 (styczeń 1993): 614–17. http://dx.doi.org/10.1142/s0217979293001293.
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We have performed Augmented Spherical Wave (ASW) calculations on bcc Mn and confirmed previous results by Moruzzi and Marcus who reported a ferrimagnetic phase. Independent computations employing the full-potential linearized-augmented-plane-wave (LAPW) method led to similar results. Our ASW results yield the total energy and the magnetic moments as a function of volume assuming different (ferro-, ferri-, antiferro-and non-magnetic) bcc related structures with type I, II, and III spin alignments. We relate the relative stability of various phases to band gaps that open at the Fermi energy for certain volumes. The LAPW symmetry-decomposed partial charges allow to analyze the binding mechanism.
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Nelson, Yarrow M., Leonard W. Lion, Michael L. Shuler i William C. Ghiorse. "Lead binding to metal oxide and organic phases of natural aquatic biofilms". Limnology and Oceanography 44, nr 7 (26.10.1999): 1715–29. http://dx.doi.org/10.4319/lo.1999.44.7.1715.
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Jayabharathi, Jayaraman, Chockalingam Karunakaran, Venugopal Thanikachalam i Periyasamy Ramanathan. "Binding and fluorescence enhancing behaviour of phenanthrimidazole with different phases of TiO2". New Journal of Chemistry 38, nr 9 (1.07.2014): 4321. http://dx.doi.org/10.1039/c4nj00610k.
Pełny tekst źródłaRozprawy doktorskie na temat "Binding phases"
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Whalley, Caroline. "Estimating binding strength and chemical phases of metals adsorbed to sediment components". Thesis, University of East Anglia, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.259990.
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Panahi, Tayyebeh. "Glutamic Acid Resorcinarene-based Molecules and Their Application in Developing New Stationary Phases in Ion Chromatography". BYU ScholarsArchive, 2016. https://scholarsarchive.byu.edu/etd/6436.
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Resorcinarenes can be functionalized at their upper and lower rims. In this work, the upper rim of a resorcinarene was functionalized with glutamic acids and the lower rim was functionalized with either methyl or undecyl alkyl groups. The cavitands were characterized by nuclear magnetic resonance (NMR), mass spectrometry (MS), UV-vis spectroscopy, dynamic light scattering (DLS) and electron microscopy. The binding of resorcinarene with amine guests was studied in DMSO by UV-vis titration. The obtained binding constants (K values) were in the range of 12,000-136000 M-1. The resorcinarenes were shown to form aggregates in a variety of solvents. The aggregates were spherical as confirmed by DLS, SEM and TEM experiments. Dynamic light scattering (DLS) experiments revealed the size of the aggregates could be controlled by cavitand concentration, pH, and temperature. The resorcinarene with undecyl alkyl group were adsorbed onto 55% cross-linked styrene-divinylbenzene resin to prepare a new stationary phases for ion chromatography (IC) columns. The new column packing material was applied in determination of uremic toxins and water contaminants. The new IC column afforded separation of the five uremic toxins : guanidinoacetic acid, guanidine, methylguanidine, creatinine, and guanidinobenzoic acid in 30 minutes. Detection and quantification of uremic toxins helps diagnose kidney problems and start patient care. Gradient elutions at ambient temperature with methanesulfonic acid (MSA) as eluent resulted in detection levels in water from 10 to 47 ppb and in synthetic urine from 28 to 180 ppb. Trace levels of creatinine (1 ppt) were detected in the urine of a healthy individual using the columns. The new IC stationary phase separated cationic pharmaceuticals including a group of guanidine compounds in surface water. Detection limits in the range of 5 - 32 µg L-1 were achieved using integrated pulsed amperometric detection (IPAD) for guanidine (G), methylguanidine (MG), 1,1-dimethylbiguanidine (DMG), agmatine (AGM), guanidinobenzoic acid (GBA) and cimetidine (CIM). Suppressed conductivity (CD) and UV-vis detection resulted in limits of detection similar to IPAD, in the range of 1.7 - 66 µg L-1, but were not able to detect all of the analytes. Three water sources, river, lake, and marsh, were analyzed and despite matrix effects, sensitivity for guanidine compounds was in the 100 µg L-1 range and apparent recoveries were 80-96 %. The peak area precision was 0.01 - 2.89% for IPAD, CD and UV-vis detection.
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Li, Weijia, i n/a. "Development of New Binding Phases for Speciation Measurements of Trace Metals with the Diffusive Gradients in Thin Films Technique". Griffith University. School of Environmental and Applied Science, 2004. http://www4.gu.edu.au:8080/adt-root/public/adt-QGU20040504.150905.
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The recently developed technique of diffusive gradients in thin films (DGT) for speciation measurement of analytes in the environment was further developed through the development of series of new binding phases including poly(acrylamide-co-acrylic acid) copolymer hydrogel (PAM-PAA), poly(acrylamidoglycolic acid-co-acrylamide) (PAAGA-PAM) hydrogel, the Whatman P81 cellulose phosphate ion exchange membrane (P81) and a liquid binding phase of poly(4-styrenesulfonate) (PSS). A new diffusion layer, cellulose dialysis membrane, was also employed for the liquid binding phase DGT. PAM-PAA copolymer hydrogel was prepared by the controlled hydrolysis of polyacrylamide (PAM) in an alkaline solution of 10% sodium hydroxide. The capacity of the copolymer hydrogel to bind various metal ions was tested under a range of uptake conditions. Ions such as Cu2+ and Cd2+ were bound more strongly to the copolymer hydrogel than the competing ions such as Na+, K+, Ca2+ and Mg2+. Metals bound to the copolymer hydrogel can be efficiently eluted in 2 M HNO3 solution (>94%). Application of this new binding material to DGT technique was validated in a synthetic lake water (Windermere, Lake District, UK) with a recovery of 99.0% for Cu2+. PAAGA-PAM hydrogel was prepared by copolymerising 2-acrylamidoglycolic acid with acrylamide. The metal ion binding properties of the hydrogel were characterised for Cu2+, Cd2+ and competing ions under various experimental conditions. The hydrogel was shown to bind Cu2+ and Cd2+ strongly under non-competitive binding conditions, with binding capacities of 5.3 and 5.1 micromol cm-2, respectively. The binding capacity of each metal decreased, under competitive binding conditions (with a range of metal ions present at 17.8 mN), to 1.3 and 0.17 micromol cm-2, respectively, indicating a strong selective binding towards Cu2+. The metal ions were readily recovered (>94%) by eluting with 2 M HNO3. Finally, the copolymer hydrogel was tested as a binding phase with the DGT technique. A linear mass vs. time relationship was observed for Cu2+ in Windermere water with a recovery of close to 100%. The use of a commercially available solid ion exchange membrane (P81) as the binding phase in DGT analysis was demonstrated. P81 is a strong cation exchange membrane. Its performance characteristics as a new binding phase in DGT measurement of Cu2+ and Cd2+ were systematically investigated. Several advantages over the conventional ion exchange resin-embedded hydrogel based binding phases used in DGT were observed. These include: simple preparation, ease of handling, and reusability. The binding phase preferentially binds to transition metal ions rather than competing ions. Within the optimum pH range (pH 4.0 - 9.0), the maximum non-competitive binding capacities of the membrane for Cu2+ and Cd2+ were 3.22 and 3.07 micromol cm-2, respectively. The suitability of the new membrane-based binding phase for DGT applications was validated experimentally. The results demonstrated excellent agreement with theoretically predicted trends. The reusability of this binding phase was also investigated. Application of a liquid binding phase and a dialysis membrane diffusive layer were proposed for the first time. The binding phase was a 0.020 M solution of poly(4-styrenesulfonate) (PSS) polyelectrolyte using a specially designed DGT device. The binding properties of Cd2+, Cu2+, and a range of alkali and alkaline earth metal ions to the PSS solution were characterised. The PSS behaved like a cation exchanger with preferential binding to Cd2+ (6.0 micromole ml-1, log K = 9.0) and Cu2+ (2.5 micromole ml-1, log K = 8.1) under competitive binding conditions. The DGT devices were successfully validated for Cd2+ and Cu2+ in Windermere water. The speciation performance of the solid and liquid binding phases developed in this study was investigated in solutions containing ethylenediaminetetraacetic acid disodium salt (EDTA), humic acid (HA), glucose (GL), dodecylbenzenesulfonic acid (DBS) and tannic acid (TA) with Cu2+ and Cd2+. The ratios of labile metals over total metals were at good agreement with calculated theoretical values using Stability Constants Database. The results indicated that the DGT-labile concentration measured by DGT with these binding phases is essentially free metal ion concentration in the sample. All newly developed DGT binding phases were successfully applied for environmental speciation. The field deployments were carried out in both freshwater and salt-water test sites.
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Westerhult, David. "Weak Affinity Chromatography : Evaluation of Different Silica Supports for Protein Immobilizationand Effect of Mobile Phases Regarding Retentionand Non-specific Binding". Thesis, Linnéuniversitetet, Institutionen för naturvetenskap, NV, 2012. http://urn.kb.se/resolve?urn=urn:nbn:se:lnu:diva-17968.
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Fragment based lead discovery (FBLD), where libraries of small fragments are screened andlater on developed to lead compounds, is an alternative to the classical drug discovery methods such as high trough-put screening. Weak affinity chromatography (WAC) is a new promising approach to the screening process of FBLD. WAC is performed by injections of fragments onto a high performance liquid chromatography (HPLC) column in which a protein is immobilized to a silica support. The retention of the injected fragments is correlated to the binding affinity of the fragments towards the immobilized protein. Immobilization capacity of three different silica materials with varying pore size (Kromasil240 Å, Nucleosil 1000 Å and Kromasil 300 Å) was evaluated by immobilization of trypsin. Retention of benzamidines on the trypsin columns was evaluated with different mobile phases. Contribution of non-specific binding in the interaction between the 4-aminobenzamidine and thrombin was estimated by frontal chromatography on a capillary columnusing PBS and PBS/acetonitrile as mobile phases. This study showed that the Kromasil 300 Å had a superior immobilization capacity of trypsin compared to the Kromasil 240 Å andthe Nucleosil 1000 Å (100 mg compared to 87.4 mg and 15.1 mg trypsin/g silica, respectively). However, the Nucleosil 1000 Å might be a more suitable support for the immobilization of larger proteins. Adding 5 % methanol or acetonitrile to the mobile phase resulted in a significant (p < 0.05) decreased retention of benzamidine fragments on the trypsin 240 Å column. Non-specific binding between thrombin and 4-ABA was not statistically significantly altered when 5 % acetonitrile was added to the mobile phase.
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Dufresne, Alice. "Modélisation atomistique de la précipitation des hydrures de zirconium : Méthodologie de developpement d'un potentiel en liaisons fortes". Thesis, Aix-Marseille, 2014. http://www.theses.fr/2014AIXM4096/document.
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Le système zirconium-hydrogène est très étudié dans le cadre de la sûreté nucléaire car la précipitation d'hydrures entraîne la fragilisation des gainages, à base d'alliage de zirconium. Il s'agit de la première barrière de confinement des produits radioactifs : son intégrité doit être maintenue tout au long de la vie des assemblages combustible, en centrale y compris en cas d'accident et post-centrale (transport et entreposage). De nombreuses incertitudes demeurent quant aux cinétiques de précipitation des hydrures et à l'impact des contraintes sur leur précipitation. La modélisation à l'échelle atomique de ce système permettrait d'apporter des clarifications sur les mécanismes en jeu. Les méthodes traditionnelles de modélisation atomistique sont basées sur des approches thermostatistiques, dont la précision et la fiabilité dépendent du potentiel interatomique qui les alimente. Or il n'existe pas de potentiel rendant possible une étude rigoureuse du système Zr-H. Cette thèse a permis de développer cet outil manquant en utilisant l'approximation des liaisons fortes. Au-delà de ce nouveau potentiel, ce travail donne un guide détaillé des nombreuses étapes d'une dérivation de tels potentiels avec la prise en compte de l'hybridation spd, ajustés ici sur des calculs DFT. Ce guide est établi tant pour un métal de transition pur que dans la perspective d'un couplage métal-covalent (carbures, nitrures et siliciures métalliques)The zirconium-hydrogen system is of nuclear safety interest, as the hydride precipitation leads to the cladding embrittlement, which is made of zirconium-based alloys. The cladding is the first safety barrier confining the radioactive products: its integrity shall be kept during the entire fuel-assemblies life, in reactor, including accidental situation, and post-operation (transport and storage). Many uncertainties remain regarding the hydrides precipitation kinectics and the local stress impact on their precipitation. The atomic scale modeling of this system would bring clarifications on the relevant mechanisms. The usual atomistic modeling methods are based on thermostatistic approaches, whose precision and reliability depend on the interatomic potential used. However, there was no potential allowing a rigorous study of the Zr-H system. The present work has indeed addressed this issue: a new tight-binding potential for zirconium hydrides modeling is now available. Moreover, this thesis provides a detailed manual for deriving such potentials accounting for spd hybridization, and fitted here on DFT results. This guidebook has be written in light of modeling a pure transition metal followed by a metal-covalent coupling (metallic carbides, nitrides and silicides)
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Palud, Amandine. "Liquid-liquid phase separation mediated by low complexity sequence domains promotes stress granule assembly and drives pathological fibrillization". Thesis, Paris 6, 2015. http://www.theses.fr/2015PA066560/document.
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Il a été observé que l’altération des fonctions des granules de stress, entités cytoplasmiques non-membranaires composées d’ARN et de protéines liant l’ARN (RBPs), peut conduire au développement de maladies telles que la sclérose latérale amyotrophique, la démence fronto-temporale, la myopathie à inclusions et la maladie de Paget des os. Ces pathologies sont caractérisées par un dépôt cytoplasmique d’inclusions solides enrichies en RBPs et comprenant des fibrilles. Une connexion génétique a été suggérée entre la persistance des granules de stress et l’accumulation de ces inclusions pathologiques dans le cytoplasme des patients. Dans mon manuscrit de thèse, il est mis en évidence le fait que la protéine hnRNPA1, dont les mutations entrainent les maladies mentionnées plus haut, subit une séparation de phases entre deux liquides connue également sous l’appellation « Séparation de Phases Liquide-Liquide » (LLPS) dans des gouttelettes enrichies en protéines. Bien que le domaine composé d’une séquence à faible complexité (Low Complexity sequence Domains ou LCD) soit suffisant pour obtenir cette séparation de phases, les domaines de liaison à l’ARN y contribuent également en présence d’ARN. Cela a permis d’envisager l’existence de plusieurs mécanismes intervenant dans la régulation de l’assemblage de ces granules. Un autre résultat a mis en exergue le fait que la formation de fibrilles n’est pas une obligation pour permettre la séparation de phases mais que les gouttelettes, enrichies en protéines, entrainent, par ailleurs, une augmentation de la formation de ces fibrilles. La séparation de phases liquide-liquide induite par le domaine composé d’une séquence à faible complexité semble contribuer à l’assemblage des granules de stress et à leurs propriétés liquides. Finalement, cette étude propose d’établir une réelle corrélation entre la formation des granules de stress qui deviennent persistants et l’accumulation d’inclusions pathologiques dans le cytoplasme des patientsStress granules are membrane-less organelles composed of RNA-binding proteins (RBPs) and RNA. Functional impairment of stress granules has been implicated in amyotrophic lateral sclerosis, inclusion body myopathy, Paget’s disease of bone and frontotemporal dementia; these diseases are characterized by solid, fibrillar, cytoplasmic inclusions that are rich in RNA binding proteins (RBPs). Genetic evidence suggests a link between persistent stress granules and the accumulation of pathological inclusions. In this thesis manuscript, I demonstrate that the disease-related RBP hnRNPA1 undergoes liquid-liquid phase separation (LLPS) into protein-rich droplets mediated by a low complexity sequence domain (LCD). While the LCD of hnRNPA1 is sufficient to mediate LLPS, the folded RNA recognition motifs contribute to LLPS in the presence of RNA, potentially giving rise to several mechanisms for regulating assembly of stress granules. Importantly, while not required for LLPS, fibrillization is enhanced in protein-rich droplets. I suggest that LCD-mediated LLPS contributes to the assembly of stress granules and their liquid properties, and provides a mechanistic link between persistent stress granules and fibrillar protein pathology in disease
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Seiser, Bernhard Josef. "Topologically close-packed phase prediction in Ni-based superalloys : phenomenological structure maps and bond-order potential theory". Thesis, University of Oxford, 2011. http://ora.ox.ac.uk/objects/uuid:4298ebde-4b32-4dcc-b294-649493f9146c.
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Single crystal nickel-based superalloys are used in modern gas turbines because of their remarkable resistance to creep deformation at elevated temperatures, which is ensured by the addition of significant amounts of refractory elements. Too high concentrations of refractory elements can lead to the formation of topologically-close packed (TCP) phases during exposure to conditions of high temperature and stress which result in the degradation of the creep properties. The traditional methods for predicting the occurrence of TCP phases in Ni-based superalloys have been based on the PHACOMP and newPHACOMP methodologies which are well-known to fail with respect to new generations of alloys. In this work a novel two-dimensional structure map (Nbar, deltaV/V) for TCP phases where Nbar is the valence-electron count and deltaV/V is a compositional dependent size factor. This map is found to separate the experimental data on the TCP phases of binary, ternary and multi-component TCP phases into well-defined regions corresponding to different structure types such as A15, sigma, chi, delta, P, R, mu, and Laves. In particular, increasing size factor separates the A15, sigma and chi phases from the delta, P, R, mu phases. The structure map is then also used in conjunction with CALPHAD computations of sigma phase stability to show that the predictive power of newPHACOMP for the seven component Ni–Co–Cr–Ta–W–Re–Al system is indeed poor. In order to gain a microscopic understanding of the observed structural trends, namely the differences between the two groups of TCP structures with increasing deltaV/V and the trend from A15 to sigma to chi with increasing Nbar, the electronic structure is coarse-grained from density functional theory (DFT) to tight-binding to bond-order potentials (BOPs). First, DFT is used to calculate the structural energy differences across the elemental 4d and 5d transition metal series and the heats of formation of the binary alloys Mo-Re, Mo-Ru, Nb-Re, and Nb-Ru. These calculations show that the valence electron concentration stabilizes A15, sigma and chi but destablizes mu and Laves phases. The latter are shown to be stabilized instead by relative size difference. Second, a simple canonical TB model and in combination with the structural energy difference theorem is found to qualitatively reproduce the energy differences predicted by the elemental DFT calculations. The structural energy difference theorem rationalizes the importance of the size factor for the stability of the mu and Laves binary phases as observed in the structure map and DFT heats of formation. Finally, analytic BOP theory, is employed to identify the structural origins of the energetic differences between TCP structure-types that lead to the trends found within the two-dimensional structure map.
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Grüner, Daniel. "Untersuchungen zur Natur der Laves-Phasen in Systemen der Übergangsmetalle". Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2007. http://nbn-resolving.de/urn:nbn:de:swb:14-1172078219643-48967.
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Laves-Phasen sind intermetallische Verbindungen der Zusammensetzung AB2, die in den Strukturtypen C14 (MgZn2), C15 (MgCu2), C36 (MgNi2) oder deren Abkömmlingen kristallisieren. Diese sind Polytypen mit einem gemeinsamen grundlegenden Strukturmuster. Insgesamt sind über 1400 binäre und ternäre Laves-Phasen bekannt. Sie stellen damit die größte Gruppe der bislang bekannten intermetallischen Verbindungen dar. Laves-Phasen wurden intensiv untersucht um grundlegende Aspekte der Phasenstabilität zu verstehen. Geometrische und elektronische Faktoren haben sich in ihrer Vorhersagekraft bezüglich des Auftretens und der Stabilität einer Laves-Phase aber nur in wenigen Fällen als hilfreich erwiesen. Das Auftreten von Homogenitätsbereichen und damit einhergehender struktureller Defekte ist in den meisten Fällen immer noch unklar und spiegelt grundsätzliche Probleme in der Chemie intermetallischer Verbindungen wider: Das unvollständige Bild der chemischen Bindung, die Tendenz zur Bildung ausgedehnter Homogenitätsbereiche sowie der Einfluss von Minoritätskomponenten auf Struktur und Phasenstabilität ist bei intermetallischen Verbindungen größer als bei vielen anderen Verbindungsklassen. Daher sind die Informationen über Struktur, Stabiblität und physikalische Eigenschaften intermetallischer Verbindungen im Allgemeinen unvollständig und mitunter unzuverlässig oder widersprüchlich. Um diese Probleme anzugehen wurden in dieser Arbeit Laves-Phasen in den Systemen Nb--TM (TM = Cr, Mn, Fe, Co) und Nb--Cr--TM (TM = Co, Ni) als Modellsysteme ausgewählt. Das Ziel der Untersuchung ist, das Wechselspiel zwischen chemischer Bindung, Struktur und Phasenstabilität für die Laves-Phasen auf der Grundlage genauer experimenteller Daten sowie quantenmechanischer Rechnungen zu beleuchten. Die Untersuchungen des binären Systems Nb--Co nehmen hier eine Schlüsselposition ein. Eine Neubestimmung des Phasendiagramms des Systems Nb--Co im Bereich der Laves-Phasen bestätigt die Existenz von Phasen mit C14-, C15- und C36-Struktur. Dabei wurden schmale Zweiphasenfelder C15 + C36 und C15 + C14 sowie ein schmaler, aber signifikanter Homogenitätsbereich der C36-Phase experimentell nachgewiesen. Die Kristallstrukturen von C36-Nb(1-x)Co(2+x) (x = 0,265), C15-Nb(1-x)Co(2+x) (x = 0,12), C15-NbCo2 und C14-Nb(1+x)Co(2-x) (x = 0,07) wurden mittels Einkristall-Röntgenstrukturanalyse verfeinert. Im Falle von C36-Nb(1-x)Co(2+x) (x = 0,265) und C15-Nb(1-x)Co(2+x) (x = 0,12) wird bestätigt, dass der Homogenitätsbereich durch Substitution von Nb durch Co erzeugt wird. Im Fall von C14-Nb(1+x)Co(2-x) werden Abweichungen von der Zusammensetzung NbCo2 durch Substitution von Co durch überschüssiges Nb erzeugt, wobei nur eine der beiden Co-Lagen gemischt besetzt wird. Quantenmechanische Rechnungen zeigen, dass dieses Besetzungsmuster energetisch bevorzugt ist. Weder mittels Röntgenbeugung noch mittels hochauflösender Elektronenmikroskopie und Elektronenbeugeng wurden Ordnungsvarianten oder Stapelvarianten der Laves-Phasen beobachtet. In der Kristallstruktur von C36-Nb(1-x)Co(2+x) (x = 0,265) ist mehr als ein Viertel des Nb durch überschüssiges Co ersetzt. Von zwei kristallographischen Nb-Lagen wird eine bevorzugt von Co besetzt, so dass sich der Co-Anteil der beiden Lagen etwa wie 2:1 verhält. Co-Antistrukturatome sind relativ zu der Nb-Position verschoben. Triebkraft dieser Verschiebungen ist die Bildung von Nb--Co-Kontakten innerhalb der A-Teilstruktur. Gemischte Besetzung der Nb-Lagen, die Verteilung der Co-Antistrukturatome und mit der Substitution einhergehende Verzerrungen führen zu einer komplizierten Realstruktur. Zur Beschreibung der elektronischen Struktur von C36-Nb(1-x)Co(2+x) (x = 0,265) werden daher verschiedene Modelle verwendet, die Tendenzen sowohl zur beobachteten Mischbesetzung als auch zur Verzerrung der Kristallstruktur aufzeigen. Die elektronische Struktur und chemische Bindung von C14-, C15- und C36-NbCo2 wurde vergleichend untersucht. Berechnungen der Gesamtenergie zeigen sehr geringe Energiedifferenzen zwischen den drei Strukturen, die mit einer sehr ähnlichen Bindungssituation der Polytypen im Einklang ist. In den Systemen Nb--Cr und Nb--Fe wurde der Verlauf der Gitterparameter innerhalb des gesamten Homogenitätsbereichs der Laves-Phase bei ausgewählten Temperaturen untersucht. Die Kristallstrukturen von C15-NbCr2 und C14-NbFe2 wurden erstmals verfeinert. Vorläufige Untersuchungen bestätigen die Existenz von zwei Hochtemperaturmodifikationen (C14 und C36) von NbCr2. Im System Nb--Mn wurde die Mn-reiche Seite des Homogenitätsbereichs bei 800 °C und 1100 °C an aus zweiphasigen (Mn(Nb) + C14) Präparaten isolierten Einkristallen untersucht. Bei 800 °C wird ein Kristall der Zusammensetzung NbMn2 erhalten, während bei 1100 °C ausgeprägte Löslichkeit von Mn in der C14-Phase beobachtet wird. Die Summenformel kann als Nb(1-x)Mn(2+x) (x = 0,13) geschrieben werden. Die Substitution von Nb durch Mn führt zu Verschiebungen der Antistrukturatome bezüglich der Nb-Lagen und damit zur Bildung kurzer Nb--Mn-Abstände. In den ternären Systemen Nb--Cr--Co und Nb--Cr--Ni wurden die Kristallstrukturen der C14-Phasen C14-Nb(Cr(1-x)Co(x))2 und C14-Nb(Cr(1-x)Ni(x))2 am Einkristall untersucht. Neben den auch für die binären C14-Phasen beobachteten Verzerrungen zeigen die Kristallstrukturen eine teilweise geordnete Verteilung von Cr und Co bzw. Cr und Ni auf die beiden kristallographischen Lagen der B-Teilstruktur. Die bevorzugte Besetzung wurde auf der Grundlage von Extended-Hückel-Rechnungen untersucht. Zwar können diese Rechnungen kein quantitatives Bild liefern, jedoch werden Tendenzen im System Nb--Cr--Co richtig wiedergegeben. Im System Nb--Cr--Ni liefern die Rechnungen jedoch dem Experiment widersprechende Ergebnisse. Die Vorhersagekraft der Methode ist also begrenzt. Vergleichende Untersuchungen der Reihe NbTM2, TM = Cr, Mn, Fe, Co mittels Röntgenabsorptionsspektroskopie und Bandstrukturrechnungen zeigen, dass die chemische Bindung der untersuchten Verbindungen im wesentlichen ähnlich ist, aber dass durchaus Entwicklungen innerhalb der Reihe festgestellt werden können. Diese Entwicklung wird besonders in der Verzerrung der C14-Phasen und hier speziell der B-Teilstruktur deutlich, die in den experimentell zugänglichen C14-Phasen in NbMn2 deutlicher ausgeprägt ist als in NbFe2. Analysen der chemischen Bindung mit Hilfe der COHP-Methoden zeigen eine ähnliche Tendenz zur Verzerrung, die vereinfacht auch als Funktion der Valenzelektronenkonzentration aufgefasst werden kann. Berechnungen der Gesamtenergie unterstützen diese Interpretation. Im Gesamtbild der elektronischen Struktur ist eine leichte Zunahme des ionischen Bindungsanteils von TM = Cr zu TM = Co zu erkennen. Die Natur der Laves-Phasen in Systemen der Übergangsmetalle ist ein sehr vielschichtiges Problem, das weiterhin intensive und interdisziplinäre Forschung erfordert. Insbesondere mit der Charakterisierung nichtstöchiometrischer Laves-Phasen wurden aber bereits wichtige Beiträge zum Verständnis der Bildung der Homogenitätsbereiche erarbeitet.
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Singh, Harmanjit. "Cytokine-binding and acute-phase plasma proteins in pigs". Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1997. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp02/NQ31901.pdf.
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Grüner, Daniel. "Untersuchungen zur Natur der Laves-Phasen in Systemen der Übergangsmetalle". Doctoral thesis, Technische Universität Dresden, 2006. https://tud.qucosa.de/id/qucosa%3A24902.
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Laves-Phasen sind intermetallische Verbindungen der Zusammensetzung AB2, die in den Strukturtypen C14 (MgZn2), C15 (MgCu2), C36 (MgNi2) oder deren Abkömmlingen kristallisieren. Diese sind Polytypen mit einem gemeinsamen grundlegenden Strukturmuster. Insgesamt sind über 1400 binäre und ternäre Laves-Phasen bekannt. Sie stellen damit die größte Gruppe der bislang bekannten intermetallischen Verbindungen dar. Laves-Phasen wurden intensiv untersucht um grundlegende Aspekte der Phasenstabilität zu verstehen. Geometrische und elektronische Faktoren haben sich in ihrer Vorhersagekraft bezüglich des Auftretens und der Stabilität einer Laves-Phase aber nur in wenigen Fällen als hilfreich erwiesen. Das Auftreten von Homogenitätsbereichen und damit einhergehender struktureller Defekte ist in den meisten Fällen immer noch unklar und spiegelt grundsätzliche Probleme in der Chemie intermetallischer Verbindungen wider: Das unvollständige Bild der chemischen Bindung, die Tendenz zur Bildung ausgedehnter Homogenitätsbereiche sowie der Einfluss von Minoritätskomponenten auf Struktur und Phasenstabilität ist bei intermetallischen Verbindungen größer als bei vielen anderen Verbindungsklassen. Daher sind die Informationen über Struktur, Stabiblität und physikalische Eigenschaften intermetallischer Verbindungen im Allgemeinen unvollständig und mitunter unzuverlässig oder widersprüchlich. Um diese Probleme anzugehen wurden in dieser Arbeit Laves-Phasen in den Systemen Nb--TM (TM = Cr, Mn, Fe, Co) und Nb--Cr--TM (TM = Co, Ni) als Modellsysteme ausgewählt. Das Ziel der Untersuchung ist, das Wechselspiel zwischen chemischer Bindung, Struktur und Phasenstabilität für die Laves-Phasen auf der Grundlage genauer experimenteller Daten sowie quantenmechanischer Rechnungen zu beleuchten. Die Untersuchungen des binären Systems Nb--Co nehmen hier eine Schlüsselposition ein. Eine Neubestimmung des Phasendiagramms des Systems Nb--Co im Bereich der Laves-Phasen bestätigt die Existenz von Phasen mit C14-, C15- und C36-Struktur. Dabei wurden schmale Zweiphasenfelder C15 + C36 und C15 + C14 sowie ein schmaler, aber signifikanter Homogenitätsbereich der C36-Phase experimentell nachgewiesen. Die Kristallstrukturen von C36-Nb(1-x)Co(2+x) (x = 0,265), C15-Nb(1-x)Co(2+x) (x = 0,12), C15-NbCo2 und C14-Nb(1+x)Co(2-x) (x = 0,07) wurden mittels Einkristall-Röntgenstrukturanalyse verfeinert. Im Falle von C36-Nb(1-x)Co(2+x) (x = 0,265) und C15-Nb(1-x)Co(2+x) (x = 0,12) wird bestätigt, dass der Homogenitätsbereich durch Substitution von Nb durch Co erzeugt wird. Im Fall von C14-Nb(1+x)Co(2-x) werden Abweichungen von der Zusammensetzung NbCo2 durch Substitution von Co durch überschüssiges Nb erzeugt, wobei nur eine der beiden Co-Lagen gemischt besetzt wird. Quantenmechanische Rechnungen zeigen, dass dieses Besetzungsmuster energetisch bevorzugt ist. Weder mittels Röntgenbeugung noch mittels hochauflösender Elektronenmikroskopie und Elektronenbeugeng wurden Ordnungsvarianten oder Stapelvarianten der Laves-Phasen beobachtet. In der Kristallstruktur von C36-Nb(1-x)Co(2+x) (x = 0,265) ist mehr als ein Viertel des Nb durch überschüssiges Co ersetzt. Von zwei kristallographischen Nb-Lagen wird eine bevorzugt von Co besetzt, so dass sich der Co-Anteil der beiden Lagen etwa wie 2:1 verhält. Co-Antistrukturatome sind relativ zu der Nb-Position verschoben. Triebkraft dieser Verschiebungen ist die Bildung von Nb--Co-Kontakten innerhalb der A-Teilstruktur. Gemischte Besetzung der Nb-Lagen, die Verteilung der Co-Antistrukturatome und mit der Substitution einhergehende Verzerrungen führen zu einer komplizierten Realstruktur. Zur Beschreibung der elektronischen Struktur von C36-Nb(1-x)Co(2+x) (x = 0,265) werden daher verschiedene Modelle verwendet, die Tendenzen sowohl zur beobachteten Mischbesetzung als auch zur Verzerrung der Kristallstruktur aufzeigen. Die elektronische Struktur und chemische Bindung von C14-, C15- und C36-NbCo2 wurde vergleichend untersucht. Berechnungen der Gesamtenergie zeigen sehr geringe Energiedifferenzen zwischen den drei Strukturen, die mit einer sehr ähnlichen Bindungssituation der Polytypen im Einklang ist. In den Systemen Nb--Cr und Nb--Fe wurde der Verlauf der Gitterparameter innerhalb des gesamten Homogenitätsbereichs der Laves-Phase bei ausgewählten Temperaturen untersucht. Die Kristallstrukturen von C15-NbCr2 und C14-NbFe2 wurden erstmals verfeinert. Vorläufige Untersuchungen bestätigen die Existenz von zwei Hochtemperaturmodifikationen (C14 und C36) von NbCr2. Im System Nb--Mn wurde die Mn-reiche Seite des Homogenitätsbereichs bei 800 °C und 1100 °C an aus zweiphasigen (Mn(Nb) + C14) Präparaten isolierten Einkristallen untersucht. Bei 800 °C wird ein Kristall der Zusammensetzung NbMn2 erhalten, während bei 1100 °C ausgeprägte Löslichkeit von Mn in der C14-Phase beobachtet wird. Die Summenformel kann als Nb(1-x)Mn(2+x) (x = 0,13) geschrieben werden. Die Substitution von Nb durch Mn führt zu Verschiebungen der Antistrukturatome bezüglich der Nb-Lagen und damit zur Bildung kurzer Nb--Mn-Abstände. In den ternären Systemen Nb--Cr--Co und Nb--Cr--Ni wurden die Kristallstrukturen der C14-Phasen C14-Nb(Cr(1-x)Co(x))2 und C14-Nb(Cr(1-x)Ni(x))2 am Einkristall untersucht. Neben den auch für die binären C14-Phasen beobachteten Verzerrungen zeigen die Kristallstrukturen eine teilweise geordnete Verteilung von Cr und Co bzw. Cr und Ni auf die beiden kristallographischen Lagen der B-Teilstruktur. Die bevorzugte Besetzung wurde auf der Grundlage von Extended-Hückel-Rechnungen untersucht. Zwar können diese Rechnungen kein quantitatives Bild liefern, jedoch werden Tendenzen im System Nb--Cr--Co richtig wiedergegeben. Im System Nb--Cr--Ni liefern die Rechnungen jedoch dem Experiment widersprechende Ergebnisse. Die Vorhersagekraft der Methode ist also begrenzt. Vergleichende Untersuchungen der Reihe NbTM2, TM = Cr, Mn, Fe, Co mittels Röntgenabsorptionsspektroskopie und Bandstrukturrechnungen zeigen, dass die chemische Bindung der untersuchten Verbindungen im wesentlichen ähnlich ist, aber dass durchaus Entwicklungen innerhalb der Reihe festgestellt werden können. Diese Entwicklung wird besonders in der Verzerrung der C14-Phasen und hier speziell der B-Teilstruktur deutlich, die in den experimentell zugänglichen C14-Phasen in NbMn2 deutlicher ausgeprägt ist als in NbFe2. Analysen der chemischen Bindung mit Hilfe der COHP-Methoden zeigen eine ähnliche Tendenz zur Verzerrung, die vereinfacht auch als Funktion der Valenzelektronenkonzentration aufgefasst werden kann. Berechnungen der Gesamtenergie unterstützen diese Interpretation. Im Gesamtbild der elektronischen Struktur ist eine leichte Zunahme des ionischen Bindungsanteils von TM = Cr zu TM = Co zu erkennen. Die Natur der Laves-Phasen in Systemen der Übergangsmetalle ist ein sehr vielschichtiges Problem, das weiterhin intensive und interdisziplinäre Forschung erfordert. Insbesondere mit der Charakterisierung nichtstöchiometrischer Laves-Phasen wurden aber bereits wichtige Beiträge zum Verständnis der Bildung der Homogenitätsbereiche erarbeitet.
Książki na temat "Binding phases"
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Tse, Season. Evaluation of commercial mass deacidification processes: AKZO-DEZ, WEI T'O, and FMC-MG3 : phase III : evaluation of media, bindings, and special paper types : report submitted to the Chairman's Committee for Preserving Documentary Heritage. Ottawa, Ont: Conservation Processes Research Division, Canadian Conservation Institute, 1994.
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Barsoum, Rashad S. Schistosomiasis. Redaktor Neil Sheerin. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199592548.003.0181_update_001.
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AbstractSchistosomes are blood flukes that parasitize humans, apes, cattle, and other animals. In these definitive hosts they are bisexual, and lay eggs which are shed to fresh water where they complete an asexual cycle in different snails, ending in the release of cercariae which infect the definitive hosts to complete the life cycle.Seven of over 100 species of schistosomes are human pathogens, causing disease in different organs depending on the parasite species. Racial and genetic factors are involved in susceptibility, severity, and sequelae of infection.Morbidity is induced by the host’s immune response to schistosomal antigens. The latter include tegument, microsomal, gut, and oval antigens. The former are important in the process of invasion and establishment of infection, oval antigens in formation of granulomata which lead to fibrosis in different sites, and the gut antigens constitute the main circulating antigens in established infection, leading to immune-complex disease, particularly in the kidneys. The host immunological response includes innate and adaptive mechanisms, the former being the front line responsible for removing 90% of the infecting cercarial load. Adaptive immunity includes a Th1 phase, dominated by activation of an acute inflammatory response, followed by a prolonged Th2 phase which is responsible for immunity to re-infection as well as progression of tissue injury. Switching from Th1 to Th2 phases is controlled by functional and morphological change in the antigen-presenting cells, which is achieved by molecules of host as well as parasitic origin.Many cells participate in parasite killing, but also in the induction of tissue injury. The most potent of these is the eosinophil, which by binding antibodies to the parasite, particularly immunoglobulin E, facilitates parasite elimination. However, this process is complex, including agonist as well as antagonist pathways, which provide escape mechanisms for the parasite to survive, thereby achieving a delicate balance that permits schistosomes to live for decades in the infected host.
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Metody badania korelacji elektronowej i uwzględniające efekty korelacyjne. Katowice: Wydawn. Uniwersytetu Śląskiego, 1994.
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Transformational Self: Attachment and the End of the Adolescent Phase. Karnac Books, 2013.
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Bendicsen, Harold K. Transformational Self: Attachment and the End of the Adolescent Phase. Taylor & Francis Group, 2018.
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Bendicsen, Harold K. Transformational Self: Attachment and the End of the Adolescent Phase. Taylor & Francis Group, 2018.
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The transformational self: Attachment and the end of the adolescent phase. Karnac, 2013.
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Fairchilde, E. M. Beginner Witch's Collection: Book of Shadows, Moon Phase Rituals Made Easy, Sabats and Esbats, Banishing, Binding, Cursing and Hexing. Independently Published, 2019.
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Kortgen, Andreas, i Michael Bauer. The effect of acute hepatic failure on drug handling in the critically ill. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199600830.003.0197.
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Impaired hepatic function is a common event in intensive care unit patients and as the liver plays a central role in drug metabolism and excretion this may lead to profound changes in pharmacokinetics. Underlying mechanisms are altered enzyme function of phase I and phase II metabolism, altered transporter protein function together with cholestasis and hepatic perfusion disorders. Moreover, multidrug therapy may lead to induction and inhibition of these enzymes and transporter proteins. In addition, changes in plasma protein binding and volumes of distribution of drugs are common. Altogether, these changes may not only lead to sometimes unpredictable plasma levels of xenobiotics, but also to drug-induced liver injury when hepatocellular accumulation of noxious substances occurs. Concomitant renal dysfunction may further complicate this situation. Pharmacodynamic alterations might also occur. In conclusion, the clinician must carefully evaluate medication given to patients with hepatic failure. Therapeutic drug monitoring should be performed wherever available to guide therapy.
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Fairchilde, E. M. Practical Witchcraft Beginner's Collection: Book of Shadows, Moon Phase Rituals Made Easy, Sabats and Esbats, and Banishing, Binding, Cursing and Hexing. Independently Published, 2019.
Znajdź pełny tekst źródłaCzęści książek na temat "Binding phases"
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Papaconstantopoulos, D. A. "Tight-Binding Hamiltonians". W Alloy Phase Stability, 351–56. Dordrecht: Springer Netherlands, 1989. http://dx.doi.org/10.1007/978-94-009-0915-1_24.
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Vuckovic, Dajana. "Solid-Phase Microextraction in Binding Studies". W Solid Phase Microextraction, 287–308. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-53598-1_10.
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Suzuki, Takashi. "Solid-Phase Binding Assay for Ganglioside Binding of Human Respiroviruses". W Methods in Molecular Biology, 179–86. New York, NY: Springer US, 2022. http://dx.doi.org/10.1007/978-1-0716-2635-1_14.
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Strauch, D. "GaN: crystal structure, phase transitions, binding energy". W New Data and Updates for IV-IV, III-V, II-VI and I-VII Compounds, their Mixed Crystals and Diluted Magnetic Semiconductors, 377–80. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-14148-5_219.
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Matrosovich, Mikhail N., i Alexandra S. Gambaryan. "Solid-Phase Assays of Receptor-Binding Specificity". W Methods in Molecular Biology, 71–94. Totowa, NJ: Humana Press, 2012. http://dx.doi.org/10.1007/978-1-61779-621-0_5.
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Gorczyńska-Zawiślan, Wioletta, Ewa Benko i Piotr Klimczyk. "CBN Composites with a Nanosized Binding Phase". W Solid State Phenomena, 149–52. Stafa: Trans Tech Publications Ltd., 2005. http://dx.doi.org/10.4028/3-908451-10-8.149.
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Pettifor, D. G., i M. Aoki. "Angularly Dependent Many-Body Potentials Within Tight Binding Hückel Theory". W Structural and Phase Stability of Alloys, 119–32. Boston, MA: Springer US, 1992. http://dx.doi.org/10.1007/978-1-4615-3382-5_8.
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Schuster, Matthias, i Siegfried Blechert. "The Allylsilyl Linker: Synthesis of Catalytic Binding of Alkenes and Alkynes to and Cleavage from Allyldimethylsilyl Polystyrene". W Solid-Phase Organic Syntheses, 139–47. New York, USA: John Wiley & Sons, Inc., 2001. http://dx.doi.org/10.1002/0471220434.ch13.
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Heubner, Arnulf, Michael Juchem, Werner Müller i Kunhard Pollow. "Application of Liquid-Liquid Partition Chromatography (LLPC) in the Preparation of Steroid Binding Proteins". W Separations Using Aqueous Phase Systems, 393–99. Boston, MA: Springer US, 1989. http://dx.doi.org/10.1007/978-1-4684-5667-7_62.
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Jones, A. M., i D. E. Brooks. "A Thermodynamic Study of the Binding of the E. coli F41 Adhesin to its Receptor, Human Glycophorin". W Separations Using Aqueous Phase Systems, 289–90. Boston, MA: Springer US, 1989. http://dx.doi.org/10.1007/978-1-4684-5667-7_46.
Pełny tekst źródłaStreszczenia konferencji na temat "Binding phases"
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Boyer-Richard, Soline, Jacky Even, Arthur Marronnier, Guido Roma, Boubacar Traoré, Claudine Katan, Laurent Pédesseau i in. "Tight-Binding modeling of CsPbI3 in several perovskite phases". W 3rd International Conference on Perovskite Thin Film Photovoltaics, Photonics and Optoelectronics. Valencia: Fundació Scito, 2017. http://dx.doi.org/10.29363/nanoge.abxpvperopto.2018.046.
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Естемесов, З. А., Б. К. Сарсенбаев, Г. О. Қаршыга, Н. Б. Сарсенбаев i А. М. Шакей. "MAIN CHARACTERISTICS OF GRANULATED PHOSPHORUS SLAG (GPS) USED FOR BINDING MATERIALS MANUFACTURING". W «АКТУАЛЬНЫЕ ВОПРОСЫ СОВРЕМЕННОЙ НАУКИ: ТЕОРИЯ, ТЕХНОЛОГИЯ, МЕТОДОЛОГИЯ И ПРАКТИКА». Международная научно-практическая онлайн-конференция, приуроченная к 60-ти летию член-корреспондента Академии наук ЧР, доктора технических наук, профессора Сайд-Альви Юсуповича Муртазаева. Crossref, 2021. http://dx.doi.org/10.34708/gstou.conf..2021.60.48.037.
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Обзорный анализ теоретических и экспериментальных известных работ показал, что ГФШ, полученный при охлаждении водой расплава с температурой 1450°С, является пористым материалом со средней плотностью 1200 кг/м3. Состоит он из трех фаз:стекло в количестве 90 - 95 %, минералы (достигает 10 %) и вредные газы (0,3 - 4 %). Благодаря повышенной гидравлической активности - ГФШ может быть использован в качестве минеральной добавки для портландцемента, одного из компонентов для шлакопортландцемента и основного компонента для шлакощелочных вяжущих с марочностью М500 и М1000 соответственно. Одновременно существуют нормативные документы, разрешающие получать вяжущие материалы без очистки и неразрешающие, если ГФШ не очищено от вредных газов. Анализ показывает необходимость применения ГФШ только в очищенном виде. The review analysis of theoretical and experimental known works showed that GPS obtained by water cooling of the melt with temperature 1450°C is a porous material with average density of 1200 kg/m3. It consists of three phases: glass in quantity 90 - 95 %, minerals (reaches 10 %) and harmful gases (0,3 - 4 %). Thanks to the increased hydraulic activity - GPS can be used as a mineral additive for Portland cement, one of the components for Portland cement slag and the basic component for slag-alkali binders with the stamps of M500 and M1000 respectively. At the same time there are normative documents allowing to receive binders without purification and unauthorized, if GPS is not purified from harmful gases. The analysis shows the necessity to use GPS only in purified form.
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Suzuki, Ken, Tomohiro Sano i Hideo Miura. "Effect of Alloying Elements on Creep and Fatigue Damage of Ni-Base Superalloy Caused by Strain-Induced Anisotropic Diffusion". W ASME 2013 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/imece2013-64314.
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In order to make clear the mechanism of the directional coarsening (rafting) of γ′ phases in Ni-base superalloys under uni-axial tensile strain, molecular dynamics (MD) analysis was applied to investigate effects of alloying elements on diffusion characteristics around the interface between the γ phase and the γ′ phase. In this study, a simple interface structure model corresponding to the γ/γ′ interface, which consisted of Ni as γ and Ni3Al as γ′ structure, was used to analyze the diffusion properties of Ni and Al atoms under tensile strain. The strain-induced anisotropic diffusion of Al atoms perpendicular to the interface between the Ni(001) layer and the Ni3Al(001) layer was observed in the MD simulation, suggesting that the strain-induced anisotropic diffusion of Al atoms in γ′ phase is one of the dominant factors of the kinetics of the rafting during creep damage. The effect of alloying elements in the Ni-base superalloy on the strain-induced anisotropic diffusion of Al atoms was also analyzed. Both the atomic radius and the binding energy with Al and Ni of the alloying element are the dominant factors that change the strain-induced diffusion of Al atoms in the Ni-base super-alloy.
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Bath, Adrian, Guido Deissmann i Stephan Jefferis. "Radioactive Contamination of Concrete: Uptake and Release of Radionuclides". W ASME 2003 9th International Conference on Radioactive Waste Management and Environmental Remediation. ASMEDC, 2003. http://dx.doi.org/10.1115/icem2003-4814.
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Concrete in nuclear installations may become contaminated by various radionuclides. Consequently, decommissioning and dismantling produce considerable quantities of potentially contaminated materials that must be managed safely and cost-effectively. In this paper we present preliminary results from a research project that aims to improve knowledge about release behaviour of radionuclides from contaminated concrete, and that proposes a scientific approach to calculating the source term for radiological dose assessment for the various management options (e.g. direct reuse, recycling, disposal of rubble). The first step is to consider which nuclides are likely to have contaminated concrete, where they might be located in concrete, and the extent to which they are chemically bound to concrete constituents. Relevant radionuclides include 60Co, 63Ni, 90Sr, 137Cs, 129I, U, Pu, Am and other actinide elements. Some nuclides are likely to be bound in specific solid phases and others are sorbed to greater or lesser degrees. The proposed modelling of releases from concrete takes into account the chemical behaviour (speciation, sorption and solubility) of the individual radionuclide contaminants and their binding to concrete phases. Other important factors that will influence release are mechanical and chemical condition of concrete, including cracking, carbonation, sulfate attack and degree of water saturation. Model calculations illustrate the potential release processes of desorption-diffusion, leaching (shrinking core model) and dissolution of discrete solid phases. For example, a scoping calculation suggests that 50-year old concrete may be contaminated with 129I to about 1 cm depth from the surface or more if the concrete is degraded, and that subsequent release will occur slowly by diffusion. Strongly sorbed or particulate nuclides such as Pu are likely to remain at the surface. Predicting the behaviour of some nuclides (e.g. Ni, U) is more uncertain because of uncertainty in the key parameters and their dependence on the local chemical conditions. Release models and source terms have been developed as the starting point for (i) the modelling of radiological consequences (i.e. dose assessments) of disposal options for building materials from nuclear installations and the optimisation of the disposal process (i.e. selection of cost-effective and reasonable disposal options), and (ii) the assessment of recycling/reuse options of slightly contaminated materials in order to reduce the amount of waste for disposal.
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Vinayak, Sundar Murugappan, Cecil Piya i Karthik Ramani. "Handy-Potter: Rapid 3D Shape Exploration Through Natural Hand Motions". W ASME 2012 International Design Engineering Technical Conferences and Computers and Information in Engineering Conference. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/detc2012-71427.
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We present the paradigm of natural and exploratory shape modeling by introducing novel 3D interactions for creating, modifying and manipulating 3D shapes using arms and hands. Though current design tools provide complex modeling functionalities, they remain non-intuitive and require significant training since they segregate 3D shapes into hierarchical 2D inputs, thus binding the user to stringent procedural steps and making modifications cumbersome. In addition the designer knows what to design when they go to CAD systems and the creative exploration in design is lost. We present a shape creation paradigm as an exploration of creative imagination and externalization of shapes, particularly in the early phases of design. We integrate the capability of humans to express 3D shapes via hand-arm motions with traditional sweep surface representation to demonstrate rapid exploration of a rich variety of fairly complex 3D shapes. We track the skeleton of users using the depth data provided by low-cost depth sensing camera (Kinect™). Our modeling tool is configurable to provide a variety of implicit constraints for shape symmetry and resolution based on the position, orientation and speed of the arms. Intuitive strategies for coarse and fine shape modifications are also proposed. We conclusively demonstrate the creation of a wide variety of product concepts and show an average modeling time of a only few seconds while retaining the intuitiveness of communicating the design intent.
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Angles-Cano, E., R. Pannell i V. Gurewich. "FIBRIN-BINDING STUDIES OF PRO-UROKINASE (PRO-UK) USING SOLID PHASE FIBRIN PLATES". W XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1642904.
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Pro-UK is a single chain urokinase-type plasminogen activator (scu-PA) which has fibrin selective thrombolytic properties. However, quantitative data on pro-UK binding to fibrin and on the mechanism of its fibrin enhanced activation of plasminogen have been difficult to obtain. In the present study, a well defined fibrin network constructed on glutaraldehyde-activated PVC plates (Anal. Biochem. 153 : 201-210, 1986) and highly purified pro-UK (99 % scu-PA) were used. Binding was investigated as follows : varying dilutions of pro-UK in the presence of a trace amount of I-labeled pro-UK in buffer without or with glu-plasminogen, plasmin or oC -thrombin and in urine, plasma or serum, were incubated overnight at 4°C and then 2 h at 37°C in the fibrin plates. After washing, the wells were cut out and counted in a gamma-counter. The labeled pro-UK and the effect of enzymes on scu-PA were investigated by SDS-PAGE and autoradiography. In parallel experiments, the activity of the fibrin bound and unbound products was investigated spectrophotometrically by adding glu-plasminogen and a synthetic substrate selective for plasmin. The binding of pro-UK to fibrin was 1.7 ± 0.1 % in buffer and 0.2 ± 0.08 % in plasma, as determined from isotopic and spectro-photometric measurements. This binding is similar to that of (0.13 ± 0.05%) two-chain urokinase (plasmin-transformed scu-PA), but is extremely low compared to the specific binding of tPA (68 - 4%). By contrast, in urine, 11.2 ± 4.47 % binding of pro-UK to fibrin was observed. Thrombin did not modify the binding but transformed scu-PA into a two-chain molecule which had lost activity. These data indicate that pro-UK has little affinity for fibrin under these conditions but that some binding may be induced by a co-factor which is present in urine. Confirmation that thrombin degrades scu-PA was obtained and it is suggested that this effect may help to regulate fibrinolysis.
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Szadkowski, Rudolf, i Jan Faigl. "Neurodynamic Sensory-Motor Phase Binding for Multi-Legged Walking Robots". W 2020 International Joint Conference on Neural Networks (IJCNN). IEEE, 2020. http://dx.doi.org/10.1109/ijcnn48605.2020.9207507.
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Tartagni, Marco, Marco Crescentini, Michele Rossi, Hywel Morgan i Enrico Sangiorgi. "An AC and phase nanowire sensing for site-binding detection". W 2014 IEEE International Electron Devices Meeting (IEDM). IEEE, 2014. http://dx.doi.org/10.1109/iedm.2014.7047146.
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Vito, A. Di, A. Pecchia, M. Auf der Maur i A. Di Carlo. "Tight binding simulations of tetragonal MAPbI3 domains within orthorhombic phase". W 2021 International Conference on Numerical Simulation of Optoelectronic Devices (NUSOD). IEEE, 2021. http://dx.doi.org/10.1109/nusod52207.2021.9541453.
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Baglia, F. A., D. Sinha i P. N. Walsh. "STRUCTURAL AND FUNCTIONAL CHARACTERIZATION OF DOMAINS IN THE HEAVY CHAIN REGION OF FACTOR XI (XIa) INVOLVED IN BINDING HIGH MOLECULAR WEIGHT KININOGEN AND FACTOR IX". W XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1642804.
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Previous studies from our laboratory (J. Biol. Chem. 260:10714,1985; J. Clin. Invest. 78:1631,1986) provide evidence that a monoclonal antibody (3C1) directed against the heavy chain region of factor XIa (FXIa) recognizes an epitope near a substrate binding site for FIX and a binding site for high molecular weight kininogen (HMWK). The present studies were carried out to determine whether these two sites are identical or different. Another heavy-chain-specific murine monoclonal antibody (5F7) was found to recognize an epitope distinct from that recognized by 3C1 since 3C1 did not compete with 5F7 for binding to FXI in a solid-phase radioimmunoassay. Antibody 3C1 was a competitive inhibitor of F-XIa-catalyzed F-IX activation, assayed by the release of a 3H-labeled activation peptide from FIX, whereas 5F7 had no effect on F—IX activation by FXIa. In contrast, 5F7 (which also inhibited F-XIIa-catalyzed F-XI activation in the presence of HMWK and kaolin) completely blocked FXI binding to immobilized HMWK at concentrations 1,000-fold lower than 3C1. Finally, HMWK had no effect on F-IX activation by FXIa. We therefore conclude that two separate and distinct domains are present in the heavy-chain region of FXI, one of which is a substrate binding site for FIX and the other a binding site for HMWK. A 15,000 Mr peptide containing the HMWK binding site was isolated using cyanogen bromide digests of factor XI which were bound to and eluted from a ,5F7 antibody affinity column and further purified using high performance liquid chromatography. Gas phase sequencing studies are in progress to characterize this peptide and place its sequence within the known structure of the heavy chain of FXIa. In conclusion, our antibodies have defined two domains within the heavy chain region of FXI: one defined by 5F7 is near the HMWK binding site, whereas the other, recognized by 3C1, is a substrate binding site for FIX. Finally, a peptide domain in the heavy chain of FXI that compriaes the HMWK binding site has been identified and isolated.
Raporty organizacyjne na temat "Binding phases"
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Yermiyahu, Uri, Thomas Kinraide i Uri Mingelgrin. Role of Binding to the Root Surface and Electrostatic Attraction in the Uptake of Heavy Metal by Plants. United States Department of Agriculture, 2000. http://dx.doi.org/10.32747/2000.7586482.bard.
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The principal accomplishment of the research supported by BARD was progress toward a comprehensive view of cell-surface electrical effects (both in cell walls [CWs] and at plasma membrane [PM] surfaces) upon ion uptake, intoxication, and amelioration. The research confirmed that electrostatic models (e.g., Gouy-Chapman-Stern [G-C-S]), with parameter values contributed by us, successfully predict ion behavior at cell surfaces. Specific research objectives 1. To characterize the sorption of selected heavy metals (Cu, Zn, Pb, Cd) to the root PM in the presence of other cations and organic ligands (citric and humic acids). 2. To compute the parameters of a G-C-S model for heavy-metal sorption to the root PM. 3. To characterize the accumulation of selected heavy metals in various plant parts. 4. To determine whether model-computed ion binding or ion activities at root PM surfaces predict heavy-metal accumulation in whole roots, root tips, or plant shoots. 5. To determine whether measured ion binding by protoplast-free roots (i.e., root CWs) predicts heavy-metal accumulation in whole roots, root tips, or plant shoots. 6. To correlate growth inhibition, and other toxic responses, with the measured and computed factors mentioned above. 7. To determine whether genotypic differences in heavy-metal accumulation and toxic responses correlate with genotypic differences in parameters of the G-C-S model. Of the original objectives, all except for objective 7 were met. Work performed to meet the other objectives, and necessitated on the basis of experimental findings, took the time that would have been required to meet objective 7. In addition, work with Pb was unsuccessful due to experimental complications and work on Cd is still in progress. On the other hand, the uptake and toxicity of the anion, selenate was characterized with respect to electrostatic effects and the influences of metal cations. In addition, the project included more theoretical work, supported by experimentation, than was originally planned. This included transmembrane ion fluxes considered in terms of PM-surface electrical potentials and the influence of CWs upon ion concentrations at PM surfaces. A important feature of the biogeochemistry of trace elements in the rhizosphere is the interaction between plant-root surfaces and the ions present in the soil solution. The ions, especially the cations, of the soil solution may be accumulated in the aqueous phases of cell surfaces external to the PMs, sometimes referred to as the "water free space" and the "Donnan free space". In addition, ions may bind to the CW components or to the PM surface with variable binding strength. Accumulation at the cell surface often leads to accumulation in other plant parts with implications for the safety and quality of foods. A G-C-S model for PMs and a Donnan-plus-binding model for CWs were used successfully to compute electrical potentials, ion binding, and ion concentration at root-cell surfaces. With these electrical potentials, corresponding values for ion activities may be computed that are at least proportional to actual values also. The computed cell-surface ion activities predict and explain ion uptake, intoxication, and amelioration of intoxication much more accurately than ion activities in the bulk-phase rooting medium.
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Kolb, Eugenia. Does the Sustainable Urban Mobility Plan (SUMP) of the European Union guarantee successful citizen participation? Goethe-Universität, Institut für Humangeographie, marzec 2021. http://dx.doi.org/10.21248/gups.51592.
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The Sustainable Urban Mobility Plan (SUMP) is a concept of the European Union. The non-binding guidelines formulated within this framework aim to help municipalities and cities to strategically define a local and long term transport and mobility plan. From the European Union's point of view, citizen participation plays a pivotal role during all phases – from the development of the plan until its implementation. This intends to achieve greater support and acceptance from the community for the plan, and to facilitate its implementation. This paper investigates whether the planning and political SUMP approach guarantees successful participatory processes, and what conclusions can be drawn to amend the SUMP process and general transport planning practice. It discusses how citizen participation is defined in the SUMP guidelines and how these elements are reflected in the SUMP guidelines of 2013 and 2019. In a second step, this paper shows how successful citizen participation is defined in an academic context and to what extent the SUMP reflects these findings. The findings derived from the academic context are then applied to the case studies of Ghent and Limburg in order to evaluate how successfully participation procedures were implemented in these SUMP processes. Finally, the question - what conclusions can be drawn from this to improve the SUMP process and general transport planning practice - is assessed.
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Boisclair, Yves R., i Arieh Gertler. Development and Use of Leptin Receptor Antagonists to Increase Appetite and Adaptive Metabolism in Ruminants. United States Department of Agriculture, styczeń 2012. http://dx.doi.org/10.32747/2012.7697120.bard.
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Objectives The original project had 2 major objectives: (1) To determine the effects of centrally administered leptin antagonist on appetite and adaptive metabolism in the sheep; (2) To develop and prepare second-generation leptin antagonists combining high binding affinity and prolonged in vivo half-life. Background Periods of suboptimal nutrition or exaggerated metabolic activity demands lead to a state of chronic energy insufficiency. Ruminants remain productive for a surprisingly long period of time under these circumstances by evoking adaptations sparing available energy and nutrients. The mechanism driving these adaptations in ruminant remains unknown, but could involve a reduction in plasma leptin, a hormone acting predominantly in the brain. In laboratory animals, reduced leptin signaling promotes survival during nutritional insufficiency by triggering energy sparing adaptations such as reduced thyroid hormone production and insulin resistance. Our overall hypothesis is that similar adaptations are triggered by reduced leptin signaling in the brain of ruminants. Testing of this hypothesis in ruminants has not been possible due to inability to block the actions of endogenous leptin and access to ruminant models where leptin antagonistic therapy is feasible and effective. Major achievements and conclusions The Israeli team had previously mutated 3 residues in ovine leptin, with no effect on receptor binding. This mutant was renamed ovine leptin antagonist (OLA) because it cannot activate signaling and therefore antagonizes the ability of wild type leptin to activate its receptor. To transform OLA into an effective in vivo antagonist, the Israeli made 2 important technical advances. First, it incorporated an additional mutation into OLA, increasing its binding affinity and thus transforming it into a super ovine leptin antagonist (SOLA). Second, the Israeli team developed a method whereby polyethylene glycol is covalently attached to SOLA (PEG-SOLA) with the goal of extending its half-life in vivo. The US team used OLA and PEG-SOLA in 2 separate animal models. First, OLA was chronically administered directly into the brain of mature sheep via a cannula implanted into the 3rdcerebroventricule. Unexpectedly, OLA had no effect of voluntary feed intake or various indicators of peripheral insulin action but reduced the plasma concentration of thyroid hormones. Second, the US team tested the effect of peripheral PEG-SOLA administration in an energy sensitive, rapidly growing lamb model. PEG-SOLA was administered for 14 consecutive days after birth or for 5 consecutive days before sacrifice on day 40 of life. Plasma PEG-SOLA had a half-life of over 16 h and circulated in 225- to 288-fold excess over endogenous leptin. PEG-SOLA administration reduced plasma thyroid hormones and resulted in a higher fat content in the carcass at slaughter, but had no effects on feed intake, body weight, plasma glucose or insulin. These results show that the team succeeded in developing a leptin antagonist with a long in vivo half-life. Moreover, in vivo results show that reduced leptin signaling promotes energy sparing in ruminants by repressing thyroid hormone production. Scientific and agricultural implications The physiological role of leptin in ruminants has been difficult to resolve because peripheral administration of wild type leptin causes little effects. Our work with leptin antagonists show for the first time in ruminants that reduced leptin signaling induces energy sparing mechanisms involving thyroid hormone production with little effect on peripheral insulin action. Additional work is needed to develop even more potent leptin antagonists, to establish optimal administration protocols and to narrow down phases of the ruminant life cycle when their use will improve productivity.
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Vouros, Paul, i Terrance Black. Solid Phase Peptide Synthesis of Antimicrobial Peptides for cell Binding Studies: Characterization Using Mass Spectrometry. Fort Belvoir, VA: Defense Technical Information Center, listopad 2002. http://dx.doi.org/10.21236/ada412571.
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Gurevitz, Michael, Michael E. Adams, Boaz Shaanan, Oren Froy, Dalia Gordon, Daewoo Lee i Yong Zhao. Interacting Domains of Anti-Insect Scorpion Toxins and their Sodium Channel Binding Sites: Structure, Cooperative Interactions with Agrochemicals, and Application. United States Department of Agriculture, grudzień 2001. http://dx.doi.org/10.32747/2001.7585190.bard.
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Integrated pest management in modern crop protection may combine chemical and biological insecticides, particularly due to the risks to the environment and livestock arising from the massive use of non-selective chemicals. Thus, there is a need for safer alternatives, which target insects more specifically. Scorpions produce anti-insect selective polypeptide toxins that are biodegradable and non-toxic to warm-blooded animals. Therefore, integration of these substances into insect pest control strategies is of major importance. Moreover, clarification of the molecular basis of this selectivity may provide valuable information pertinent to their receptor sites and to the future design of peptidomimetic anti-insect specific substances. These toxins may also be important for reducing the current overuse of chemical insecticides if they produce a synergistic effect with conventional pesticides. Based on these considerations, our major objectives were: 1) To elucidate the three-dimensional structure and toxic-site of scorpion excitatory, "depressant, and anti-insect alpha toxins. 2) To obtain an initial view to the sodium channel recognition sites of the above toxins by generating peptide decoys through a phage display system. 3) To investigate the synergism between toxins and chemical insecticides. Our approach was to develop a suitable expression system for toxin production in a recombinant form and for elucidation of toxin bioactive sites via mutagenesis. In parallel, the mode of action and synergistic effects of scorpion insecticidal toxins with pyrethroids were studied at the sodium channel level using electrophysiological methods. Objective 1 was achieved for the alpha toxin, LqhaIT Zilberberg et al., 1996, 1997; Tugarinov et al., 1997; Froy et al., 2002), and the excitatory toxin, Bj-xtrIT (Oren et al., 1998; Froy et al., 1999; unpublished data). The bioactive surface of the depressant toxin, LqhIT2, has been clarified and a crystal of the toxin is now being analyzed (unpublished). Objective 2 was not successful thus far as no phages that recognize the toxins were obtained. We therefore initiated recently an alternative approach, which is introduction of mutations into recombinant channels and creation of channel chimeras. Objective 3 was undertaken at Riverside and the results demonstrated synergism between LqhaIT or AaIT and pyrethroids (Lee et al., 2002). Furthermore, negative cross-resistance between pyrethroids and scorpion toxins (LqhaIT and AaIT) was demonstrated at the molecular level. Although our study did not yield a product, it paves the way for future design of selective pesticides by capitalizing on the natural competence of scorpion toxins to distinguish between sodium channels of insects and vertebrates. We also show that future application of anti-insect toxins may enable to decrease the amounts of chemical pesticides due to their synergism.
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Meidan, Rina, i Robert Milvae. Regulation of Bovine Corpus Luteum Function. United States Department of Agriculture, marzec 1995. http://dx.doi.org/10.32747/1995.7604935.bard.
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The main goal of this research plan was to elucidate regulatory mechanisms controlling the development, function of the bovine corpus luteum (CL). The CL contains two different sterodigenic cell types and therefore it was necessary to obtain pure cell population. A system was developed in which granulosa and theca interna cells, isolated from a preovulatory follicle, acquired characteristics typical of large (LL) and small (SL) luteal cells, respectively, as judged by several biochemical and morphological criteria. Experiments were conducted to determine the effects of granulosa cells removal on subsequent CL function, the results obtained support the concept that granulosa cells make a substaintial contribution to the output of progesterone by the cyclic CL but may have a limited role in determining the functional lifespan of the CL. This experimental model was also used to better understand the contribution of follicular granulosa cells to subsequent luteal SCC mRNA expression. The mitochondrial cytochrome side-chain cleavage enzyme (SCC), which converts cholesterol to pregnenolone, is the first and rate-limiting enzyme of the steroidogenic pathway. Experiments were conducted to characterize the gene expression of P450scc in bovine CL. Levels of P450scc mRNA were higher during mid-luteal phase than in either the early or late luteal phases. PGF 2a injection decreased luteal P450scc mRNA in a time-dependent manner; levels were significantly reduced by 2h after treatment. CLs obtained from heifers on day 8 of the estrous cycle which had granulosa cells removed had a 45% reduction in the levels of mRNA for SCC enzymes as well as a 78% reduction in the numbers of LL cells. To characterize SCC expression in each steroidogenic cell type we utilized pure cell populations. Upon luteinization, LL expressed 2-3 fold higher amounts of both SCC enzymes mRNAs than SL. Moreover, eight days after stimulant removal, LL retained their P4 production capacity, expressed P450scc mRNA and contained this protein. In our attempts to establish the in vitro luteinization model, we had to select the prevulatory and pre-gonadotropin surge follicles. The ratio of estradiol:P4 which is often used was unreliable since P4 levels are high in atretic follicles and also in preovulatory post-gonadotropin follicles. We have therefore examined whether oxytocin (OT) levels in follicular fluids could enhance our ability to correctly and easily define follicular status. Based on E2 and OT concentrations in follicular fluids we could more accurately identify follicles that are preovulatory and post gonadotropin surge. Next we studied OT biosynthesis in granulosa cells, cells which were incubated with forskolin contained stores of the precursor indicating that forskolin (which mimics gonadotropin action) is an effective stimulator of OT biosynthesis and release. While studying in vitro luteinization, we noticed that IGF-I induced effects were not identical to those induced by insulin despite the fact that megadoses of insulin were used. This was the first indication that the cells may secrete IGF binding protein(s) which regonize IGFs and not insulin. In a detailed study involving several techniques, we characterized the species of IGF binding proteins secreted by luteal cells. The effects of exogenous polyunsaturated fatty acids and arachidonic acid on the production of P4 and prostanoids by dispersed bovine luteal cells was examined. The addition of eicosapentaenoic acid and arachidonic acid resulted in a dose-dependent reduction in basal and LH-stimulated biosynthesis of P4 and PGI2 and an increase in production of PGF 2a and 5-HETE production. Indomethacin, an inhibitor of arachidonic acid metabolism via the production of 5-HETE was unaffected. Results of these experiments suggest that the inhibitory effect of arachidonic acid on the biosynthesis of luteal P4 is due to either a direct action of arachidonic acid, or its conversion to 5-HETE via the lipoxgenase pathway of metabolism. The detailed and important information gained by the two labs elucidated the mode of action of factors crucially important to the function of the bovine CL. The data indicate that follicular granulosa cells make a major contribution to numbers of large luteal cells, OT and basal P4 production, as well as the content of cytochrome P450 scc. Granulosa-derived large luteal cells have distinct features: when luteinized, the cell no longer possesses LH receptors, its cAMP response is diminished yet P4 synthesis is sustained. This may imply that maintenance of P4 (even in the absence of a Luteotropic signal) during critical periods such as pregnancy recognition, is dependent on the proper luteinization and function of the large luteal cell.
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Sebesta, F., J. John i A. Motl. Phase 2 report on the evaluation of polyacrylonitrile (PAN) as a binding polymer for absorbers used to treat liquid radioactive wastes. Office of Scientific and Technical Information (OSTI), maj 1996. http://dx.doi.org/10.2172/231361.
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Levy, Avraham A., i Virginia Walbot. Regulation of Transposable Element Activities during Plant Development. United States Department of Agriculture, sierpień 1992. http://dx.doi.org/10.32747/1992.7568091.bard.
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We have studied the regulation of the maize Ac and MuDR transposable elements activities during plant development. Ac was studied in an heterologous system (transgenic tobacco plants and cell suspensions) while MuDR was studied in the native maize background. The focus of this study was on the transcriptional regulation of Ac and MuDR. For Ac, the major achievements were to show that 1-It is autoregulated in a way that the Ac-encoded transposase can repress the activity of its own promoter; 2-It is expressed at low basal level in all the plant organs that were studied, and its activity is stronger in dividing tissues -- a behaviour reminiscent of housekeeping genes; 3- the activity of Ac promoter is cell cycle regulated -- induced at early S-phase and increasing until mitosis; 4- host factor binding sites were identified at both extremities of Ac and may be important for transposition. For MuDR, It was shown that it encodes two genes, mudrA and mudrB, convergently transcribed from near-identical promoters in the terminal inverted repeats. Distinct 5' start sites, alternative splicing, production of antisense RNA and tissue specificity were all shown to be involved in the regulation of MuDR.
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Barg, Rivka, Erich Grotewold i Yechiam Salts. Regulation of Tomato Fruit Development by Interacting MYB Proteins. United States Department of Agriculture, styczeń 2012. http://dx.doi.org/10.32747/2012.7592647.bard.
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Background to the topic: Early tomato fruit development is executed via extensive cell divisions followed by cell expansion concomitantly with endoreduplication. The signals involved in activating the different modes of growth during fruit development are still inadequately understood. Addressing this developmental process, we identified SlFSM1 as a gene expressed specifically during the cell-division dependent stages of fruit development. SlFSM1 is the founder of a class of small plant specific proteins containing a divergent SANT/MYB domain (Barg et al 2005). Before initiating this project, we found that low ectopic over-expression (OEX) of SlFSM1 leads to a significant decrease in the final size of the cells in mature leaves and fruits, and the outer pericarp is substantially narrower, suggesting a role in determining cell size and shape. We also found the interacting partners of the Arabidopsis homologs of FSM1 (two, belonging to the same family), and cloned their tomato single homolog, which we named SlFSB1 (Fruit SANT/MYB–Binding1). SlFSB1 is a novel plant specific single MYB-like protein, which function was unknown. The present project aimed at elucidating the function and mode of action of these two single MYB proteins in regulating tomato fruit development. The specific objectives were: 1. Functional analysis of SlFSM1 and its interacting protein SlFSB1 in relation to fruit development. 2. Identification of the SlFSM1 and/or SlFSB1 cellular targets. The plan of work included: 1) Detailed phenotypic, histological and cellular analyses of plants ectopically expressing FSM1, and plants either ectopically over-expressing or silenced for FSB1. 2) Extensive SELEX analysis, which did not reveal any specific DNA target of SlFSM1 binding, hence the originally offered ChIP analysis was omitted. 3) Genome-wide transcriptional impact of gain- and loss- of SlFSM1 and SlFSB1 function by Affymetrix microarray analyses. This part is still in progress and therefore results are not reported, 4) Search for additional candidate partners of SlFSB1 revealed SlMYBI to be an alternative partner of FSB1, and 5) Study of the physical basis of the interaction between SlFSM1 and SlFSB1 and between FSB1 and MYBI. Major conclusions, solutions, achievements: We established that FSM1 negatively affects cell expansion, particularly of those cells with the highest potential to expand, such as the ones residing inner to the vascular bundles in the fruit pericarp. On the other hand, FSB1 which is expressed throughout fruit development acts as a positive regulator of cell expansion. It was also established that besides interacting with FSM1, FSB1 interacts also with the transcription factor MYBI, and that the formation of the FSB1-MYBI complex is competed by FSM1, which recognizes in FSB1 the same region as MYBI does. Based on these findings a model was developed explaining the role of this novel network of the three different MYB containing proteins FSM1/FSB1/MYBI in the control of tomato cell expansion, particularly during fruit development. In short, during early stages of fruit development (Phase II), the formation of the FSM1-FSB1 complex serves to restrict the expansion of the cells with the greatest expansion potential, those non-dividing cells residing in the inner mesocarp layers of the pericarp. Alternatively, during growth phase III, after transcription of FSM1 sharply declines, FSB1, possibly through complexing with the transcription factor MYBI serves as a positive regulator of the differential cell expansion which drives fruit enlargement during this phase. Additionally, a novel mechanism was revealed by which competing MYB-MYB interactions could participate in the control of gene expression. Implications, both scientific and agricultural: The demonstrated role of the FSM1/FSB1/MYBI complex in controlling differential cell growth in the developing tomato fruit highlights potential exploitations of these genes for improving fruit quality characteristics. Modulation of expression of these genes or their paralogs in other organs could serve to modify leaf and canopy architecture in various crops.
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Gershoni, Jonathan M., David E. Swayne, Tal Pupko, Shimon Perk, Alexander Panshin, Avishai Lublin i Natalia Golander. Discovery and reconstitution of cross-reactive vaccine targets for H5 and H9 avian influenza. United States Department of Agriculture, styczeń 2015. http://dx.doi.org/10.32747/2015.7699854.bard.
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Research objectives: Identification of highly conserved B-cell epitopes common to either H5 or H9 subtypes of AI Reconstruction of conserved epitopes from (1) as recombinantimmunogens, and testing their suitability to be used as universal vaccine components by measuring their binding to Influenza vaccinated sera of birds Vaccination of chickens with reconstituted epitopes and evaluation of successful vaccination, clinical protection and viral replication Development of a platform to investigate the dynamics of immune response towards infection or an epitope based vaccine Estimate our ability to focus the immune response towards an epitope-based vaccine using the tool we have developed in (D) Summary: This study is a multi-disciplinary study of four-way collaboration; The SERPL, USDA, Kimron-Israel, and two groups at TAU with the purpose of evaluating the production and implementation of epitope based vaccines against avian influenza (AI). Systematic analysis of the influenza viral spike led to the production of a highly conserved epitope situated at the hinge of the HA antigen designated “cluster 300” (c300). This epitope consists of a total of 31 residues and was initially expressed as a fusion protein of the Protein 8 major protein of the bacteriophagefd. Two versions of the c300 were produced to correspond to the H5 and H9 antigens respectively as well as scrambled versions that were identical with regard to amino acid composition yet with varied linear sequence (these served as negative controls). The recombinantimmunogens were produced first as phage fusions and then subsequently as fusions with maltose binding protein (MBP) or glutathioneS-transferase (GST). The latter were used to immunize and boost chickens at SERPL and Kimron. Furthermore, vaccinated and control chickens were challenged with concordant influenza strains at Kimron and SEPRL. Polyclonal sera were obtained for further analyses at TAU and computational bioinformatics analyses in collaboration with Prof. Pupko. Moreover, the degree of protection afforded by the vaccination was determined. Unfortunately, no protection could be demonstrated. In parallel to the main theme of the study, the TAU team (Gershoni and Pupko) designed and developed a novel methodology for the systematic analysis of the antibody composition of polyclonal sera (Deep Panning) which is essential for the analyses of the humoral response towards vaccination and challenge. Deep Panning is currently being used to monitor the polyclonal sera derived from the vaccination studies conducted at the SEPRL and Kimron.