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Query: UMLS:C0276640 (TEM)
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The two snake venom myotoxins ammodytin L and myotoxin II, purified respectively from Vipera ammodytes ammodytes and Bothrops asper, have phospholipase-like structures but lack an Asp-49 in the active site and are without normal phospholipase activity. The interaction of these proteins with different types of liposomes indicated that the myotoxins were able to provoke rapid and extensive release of the aqueous content of liposomes. Leakage was measured by two different methods: fluorescence dequenching of liposome-entrapped carboxyfluorescein and ESR measurement of intravesicular TEM-POcholine reduction by external ascorbate. The process was independent of Ca2+ and took place without any detectable phospholipid hydrolysis. Nonmyotoxic phospholipases tested under the same conditions were unable to induce liposome leakage, which could be detected only when Ca2+ was added to the medium and with the concomitant hydrolysis of phospholipids. The kinetics of Ca(2+)-dependent and Ca(2+)-independent leakage were completely different, indicating two different mechanisms of interaction with the lipid bilayer. Studies using diphenylhexatriene as a probe of lipid membrane organization indicated that the myotoxins gave rise to a profound perturbation of the arrangement of the lipid chains in the membrane interior, whereas interaction of Naja naja phospholipase A2 with the membrane surface did not affect lipid organization. On the basis of these results we suggest that a new type of cytolytic reaction mechanism is responsible for the effects of phospholipase-like myotoxins in vivo.
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PMID:Calcium ion independent membrane leakage induced by phospholipase-like myotoxins. 133 27

We have examined the epididymal (caput, corpus and cauda) and ejaculated spermatozoa of bufallo-bull (Bubalus bubalis) employing microscopic and spectroscopic techniques. Fluorescein isothiocyanate conjugated lectins namely concanavalin A (Con A), Dolichos biflorus (DBA), Maclura pomifera (MPA), peanut agglutinin (PNA), soybean agglutinin (SBA) and wheat germ agglutinin (WGA) were used to study the changes in the sperm surface carbohydrate make up as the spermatozoa mature. Quantitative analysis of the lectin binding was made flow cytometrically. 31P-NMR (nuclear magnetic resonance) spectra of the sperms obtained from different regions (head, body and tail) of the epididymis and of the ejaculate were analyzed to assess their metabolic activity. And the kinetics of spin label reduction of these samples was monitored with ESR (electron spin resonance) spectroscopy. These observations are supplemented with the electron microscopic (SEM and TEM) examination of the epididymal and ejaculated spermatozoa.
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PMID:Spectroscopic and microscopic studies of buffalo-bull (Bubalus bubalis) spermatozoa. 838 30

The mesoporous MnSBA-15 materials with different n(Si)/n(Mn) ratios of 4, 8, 20, and 50 have been synthesized, for the first time, using manganese nitrate tetrahydrate and Pluronic 123 triblock polymer [(EO)20(PO)70(EO)20] by simply adjusting the molar ratio of water to hydrochloric acid (n(H2O)/n(HCl)) under direct hydrothermal conditions. For the effect of structural and textural properties with incorporation of manganese, the MnSBA-15 has been synthesized with different synthesis temperatures at the fixed molar ratios of n(Si)/n(Mn) = 4 and n(H2O)/n(HCl) = 295 in the synthesis gel. The hydrothermal and thermal stabilities of MnSBA-15 have also been investigated. The calcined MnSBA-15 materials prepared have been characterized by ICP-AES, XRD, N2 adsorption, ESR, FE-SEM, and TEM. The ICP-AES studies show a higher amount of manganese incorporation on the silica pore walls, as MnSBA-15 with a n(Si)/n(Mn) ratio up to 2.2 can be successfully prepared at a fixed n(H2O)/n(HCl) molar ratio of 295 by adjusting the ratios of n(Si)/n(Mn) in the synthesis gel. The structural and textural properties of calcined MnSBA-15 prepared can be found by the results of XRD and N2 adsorption. The investigation of ESR results clearly describe the effect of structure and Mn species coordination on the SBA-15 silica pore walls while the uniform pore diameter and rope-like hexagonal mesoporous structure of MnSBA-15 can be identified by TEM and FE-SEM images. With increasing synthesis temperature, an increase the unit cell parameter, pore size, and pore volume and a decrease the specific surface area and pore wall thickness of MnSBA-15 can be obviously noted by the results of XRD and N2 adsorption. The hexagonal MnSBA-15 materials prepared could be tested as catalysts in epoxidation of trans-stilbene to produce trans-stilbene oxide under various optimal conditions while their catalytic properties could also be compared to the results of MnMCM-41 and ZrMnMCM-41.
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PMID:Direct synthesis of well-ordered and unusually reactive MnSBA-15 mesoporous molecular sieves with high manganese content. 1706 42

A technology, microwave-assisted photocatalysis on TiO(2) nanotubes, which can be applied to degrade atrazine rapidly and completely, was investigated. TiO(2) nanotubes were prepared, and confirmed by XRD, TEM and ESR. Microwave-assisted photocatalytic degradation of atrazine in aqueous solution was investigated. The result indicates that atrazine is completely degraded in 5min and the mineralization efficiency is 98.5% in 20min, which is obviously more efficient than that by the traditional photocatalytic degradation methods. It may be attributed to the intense UV radiation generated by electrodeless discharge lamps under microwave irradiation, the increased number of OH, additional defect sites on TiO(2) under the irradiation of microwave and larger specific surface area of TiO(2) nanotubes which could adsorb more organic substances to degrade than TiO(2) nanoparticles. Along with the degradation of atrazine, the concentrations of Cl(-) and NO(3)(-) increase gradually. In 20min [Cl(-)] and [NO(3)(-)] are 3, 27.8mg/L, respectively, which are close to their stoichiometric values. The major intermediates of atrazine were identified by HPLC/MS and possible degradation pathways of atrazine in microwave-assisted photocatalysis on TiO(2) nanotubes were proposed.
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PMID:Microwave assisted rapid and complete degradation of atrazine using TiO(2) nanotube photocatalyst suspensions. 1718 29

Micelle formation induced by disproportionation was attained for a diblock copolymer containing 2,2,6,6-tetramethylpyperidine-1-oxyl (TEMPO). Poly(4-vinylbenzyloxy-TEMPO)-block-polystyrene (PVTEMPO-b-PSt) showed no self-assembly in 1,4-dioxane, a nonselective solvent. Light scattering studies demonstrated that the copolymer self-assembled into micelles in this solvent with the addition of hydrochloric acid (HCl). The hydrodynamic diameter of the copolymer was estimated to be ca. 55 nm based on the cumulant analysis of the complete micellization. A UV analysis confirmed that the micellizarion proceeded through the disproportionation of the TEMPO into the oxoaminium chloride and the hydroxylamine by the reaction with HCl, because the absorption based on the oxoaminium chloride increased with an increase in the amount of HCl. ESR verified that the radical concentration of the TEMPO decreased with an increase in the HCl. Before the addition of HCl, the PVTEMPO-b-PSt copolymer showed broad signals based on the random orientation. As the amount of HCl increased, the broad signals changed to the typical triplet of TEMPO, accompanied by a decrease in the signal intensity. The g values had a negligible change throughout the micellization. Finally, 40% of the TEMPO remained unreacted when the micellization was completed. The micellization prevented the dispropotionation of the TEMPO, because the PVTEMPO blocks formed the micellar cores which were covered with the micellar coronas of the PSt blocks. TEM observations demonstrated that PVTEMPO-b-PSt formed spherical micelles through the dispropotionation-induced micellization.
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PMID:Micelle formation induced by disproportionation of stable nitroxyl radicals supported on a diblock copolymer. 1789 95

Nanoparticles of Zn1-xCuxS with Cu concentrations of x=0.0, 0.1, 0.2, 0.3 and 0.4 were prepared by a co-precipitation reaction method from homogeneous solutions of zinc and copper salts. Both the ZnS and ZnS:Cu nanoparticles excited at about 370 nm exhibits a broad green emission band peaking around 491 nm, which confirms the characteristic feature of Zn2+ as well as Cu2+ ions as luminescent centers in the lattice. The TEM micrographs showed spherical morphology for ZnS nanocrystals and the average size of the particles was estimated to be around 8.5 nm. At liquid nitrogen temperature, ESR signal characteristic of Cu2+ ions was observed in samples of all concentrations. ESR spectra analysis also indicated that Cu2+ ions enter the host lattice by replacing Zn2+ ions with distorted tetrahedral site symmetry.
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PMID:ESR and photoluminescence properties of Cu doped ZnS nanoparticles. 1860 63

The cross-linked polyurea support EnCat 30, its related macromolecular complex Pd(II)/EnCat 30 and its related Pd(0)/EnCat 30NP nanocomposite are thoroughly investigated with SEM, TEM, ISEC and ESR in the solid state (SEM and TEM) and swollen state in THF (ISEC and ESR). Pd(II)/EnCat 30 and its related Pd(0)/EnCat 30NP are obtained by microencapsulation of palladium acetate in a polyurea framework, which is formed upon hydrolysis/condensation of mixtures of multi-functional oligo-arylisocyanates in dichloroethane. Most remarkably, both Pd(II)/EnCat and Pd(0)/EnCat 30NP turn out to be far more (nano)porous and swellable materials than the blank polyurea matrix (EnCat 30). It is proposed that there is a strong nanostructural effect exerted by Pd(II) species due to its interaction with functional groups (amines stemming from the hydrolysis of the isocyanato groups or ureido groups belonging to the polymer chains) during the growth of the cross-linked polymer framework. As a consequence, the catalytic species in both Pd(II)/EnCat 30 and Pd(0)/EnCat 30NP are much more accessible to molecules diffusing from liquid phases in contact with the materials and, hence, are better catalysts than expected from the morphology of blank polyurea EnCat 30.
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PMID:Cross-linked polyvinyl polymers versus polyureas as designed supports for catalytically active M(0) nanoclusters. Part III. Nanometer scale structure of the cross-linked polyurea support EnCat 30 and of the Pd(II)/EnCat 30 and Pd(0)/EnCat 30NP catalysts. 1944 Jun 37

F-Si-co-modified TiO(2) (FST) samples with different ratios of fluorine to titanium (R(F)) and silica to titanium (R(x)), were successfully synthesized by ultrasound-assisted hydrolysis. The structure and properties of the as-prepared codoped titania were characterized by means of XRD, TEM, XPS, BET, UV-Vis diffuse reflectance spectra and ESR. XRD analysis showed that Si and F atoms prevented phase transition of anatase to rutile and suppressed the growth of titania crystalline. ESR results showed that the concentration of the active species (.OH) on 1%-FST(R(x)=10%) was higher than that on other FST samples and P25 titania. The improvement in photocatalytic activity relative to titania can be achieved by co-modifying fluorine and silica to fabricate FST composite material. The photocatalytic activity of FST powders for decomposition of methyl orange was affected by the content of fluorine and the content of silica. When the ratios of R(F) and R(x) were 1 and 10%, respectively, 1%-FST(R(x)=10%) shows the best among photocatalytic activity, which is much superior to P25 under UV-Vis irradiation. The possible reasons for the high photocatalytic activity of the FST powders were proposed in the paper. In addition, the stability of the FST powders in photocatalytic process was confirmed based on the XPS analysis.
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PMID:Enhanced photocatalytic activity for titanium dioxide by co-modifying with silica and fluorine. 1986 60

This work represents a new method to synthesis of ZnO and/or Zn nanoparticles by means of microwave plasma whose electrons are the reducing agents. Glass quadratic slides sized 2.5 x 2.5 cm were coated by ZnO and/or Zn particles whose sizes ranged from a few micrometers to approximately 20 nm. The size of the particles can be controlled by the type of the precursor and its concentration. In the current paper, the mechanism of the reactions of ZnO and/or Zn formation was proposed. Longer plasma irradiation and lower precursor concentration favor the fabrication of metallic Zn nanoparticles. The nature of the precursor's ion (acetate, nitrate, or chloride) is also of importance in determining the composition of the product. The glass slides coated by ZnO and/or Zn nanoparticles were characterized by HR-SEM, HR-TEM, AFM, XRD, ESR, contact angle and diffuse reflectance spectroscopy (DRS).
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PMID:Synthesis of ZnO and Zn nanoparticles in microwave plasma and their deposition on glass slides. 2033 10

With a view to investigate the structural, electronic and magnetic properties of Ni (5%) doped SnO(2) diluted magnetic semiconductor nanorods prepared by a PEG-6000 assisted wet chemical route, a systematic investigation has been carried out. The micro structural properties were investigated by Rietveld refinement of XRD data, AFM, TEM, EDS, SAED, FTIR, Raman scattering and XPS measurements. These studies revealed that Sn0.95Ni0.05O2 nanorods have a polycrystalline single phase tetragonal rutile structure without any detectable impurity phases and the aspect ratios of the nanorods are in the range 2.85-10.2. The deconvoluted XPS core level Ni 2p spectral studies determined the oxidation state of Ni as +2. The nanosize effects and local defects are found to influence the local electronic structure of materials. From M-H, M-T, magnetic force microscopy (MFM) and ESR studies, all the samples are found to exhibit clear room temperature ferromagnetism without any metallic clusters. The magnetization behaviour is found to depend on the overlap of percolated bound magnetic polarons and their interactions with dopant induced defects. The magnetic exchange interactions are found to depend on the aggregation behaviour of nanorods, exchange media, the surface diffusion behaviour of randomly distributed Ni ions and the modification of electronic structure.
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PMID:Structural, electronic and magnetic properties of Sn0.95Ni0.05O2 nanorods. 2113 72


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