Search results for "layer"

showing 10 items of 2667 documents

The amphipathic peptide mellitin as a tool to study the membrane-dependent activation of tissue transglutaminase

2001

The role of membrane phospholipids on the cross-linking activity of guinea pig liver (tissue) transglutaminase has been investigated using the amphipathic model peptide melittin as glutaminyl substrate and the primary amine monodansylcadaverine as extrinsic amine donor. A marked increase of transglutaminase catalytic activity was observedin vitro assays in the presence of neutral membrane phospholipids. In contrast, activation was abolished in the presence of membranes containing pure anionic lipids. Enzyme activation could be ascribed to a direct binding of the lipid to the protein as demonstrated in enzymatic assays using a non membrane-interacting peptide (Cbz-Gln-Gly). The data obtained…

chemistry.chemical_classificationbiologyTissue transglutaminaseBioengineeringPeptideBiochemistryMelittinIn vitroAnalytical ChemistryEnzyme activatorchemistry.chemical_compoundMembranechemistryBiochemistryDrug DiscoveryAmphiphilebiology.proteinMolecular Medicinelipids (amino acids peptides and proteins)Lipid bilayerLetters in Peptide Science
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Kultivierung humaner Zellen auf polymerbeschichteten Bioimplantaten?ein neues Konzept zur Verbesserung der Implantateigenschaften

2004

BACKGROUND AND PURPOSE Calcific degeneration with the resulting need for operative replacement remains the major drawback of bioprostheses. Previous studies have shown that cellular surface seeding decreases calcium uptake in vitro and in vivo, but complete coverage remains difficult to achieve. A new approach is presented, masking glutaraldehyde residues with a covalently bound polymer layer thus facilitating cell seeding. The aim of this study was to evaluate different polymers for their ability to promote surface cell adhesion and formation of complete monolayers. MATERIAL AND METHODS Ten ultrathin polymers, covalently bound to glass and exhibiting different physicochemical characteristi…

chemistry.chemical_classificationbusiness.industryCell growthScanning electron microscopeBiomaterialPolymerchemistry.chemical_compoundchemistryCovalent bondMonolayerBiophysicsMedicineGlutaraldehydeCardiology and Cardiovascular MedicineCell adhesionbusinessHerz
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Effective Removal and Mineralization of 8-Hydroxyquinoline-5-sulfonic Acid through a Pressurized Electro-Fenton-like Process with Ni−Cu−Al Layered Do…

2020

Ni−Cu−Al layered double hydroxide (Ni−Cu−Al LDH) was proposed as an electro‐Fenton‐like catalyst for 8‐hydroxyquinoline‐5‐sulfonic acid (8‐HQS) removal in water. The properties of the prepared catalysts were characterized by using X‐ray, SEM and EDAX analyses. The effect of numerous operative parameters on the removal of 8‐HQS and total organic carbon (TOC) was studied. Very high level removal of both 8‐HQS and TOC (87 and 79 %, respectively) were obtained by using a pressurized electro‐Fenton‐like process (PrEFL‐LDH) at P=10 bars, using a Ti/IrO2‐Ta2O5 anode for 6 h. The process presented good performances in a large range of pH (3–10) and gave better removals of 8‐HQS and TOC with respect…

chemistry.chemical_classificationchemistry.chemical_compoundChemistry8-hydroxyquinoline-5-sulfonic acid heterogeneous catalysis Ni−Cu−Al layered double hydroxide nitrogen heterocycles pressurized-electro-FentonElectrochemistryHydroxide8-HydroxyquinolineMineralization (soil science)Sulfonic acidSettore ING-IND/27 - Chimica Industriale E TecnologicaHeterogeneous catalysisCatalysisNuclear chemistry
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X-Ray Scattering Studies of Organic Monolayers on Electrolytic Solutions: Arachidic Acid on CdCl2

1992

The interaction between a charged monolayer of fatty acid molecules on the surface of a CdCl2 aqueous solution and the ions below has been investigated by means of X-ray Reflection and Grazing-Incidence Diffraction. A stoichiometric, localised layer of Cd++ ions forms an epitaxial 2×3 superstructure below the 2D-crystalline fatty acid monolayer.

chemistry.chemical_classificationchemistry.chemical_compoundMaterials scienceAqueous solutionchemistryMonolayerInorganic chemistryArachidic acidMoleculeFatty acidElectrolyteSuperstructure (condensed matter)Stoichiometry
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Defect-Free Chemical Functionalization of Magnetic Monolayers Based on Coordination Polymers

2018

<p>Chemical functionalization has demonstrated to be a powerful approach to tailor the physical and chemical properties of two-dimensional (2D) materials, to increase their processability and</p> <p>stability, to add new functionalities and, even, to create new 2D materials. However, this post synthetic method – which involves the anchoring of molecules on the surface of an exfoliated 2D crystal – inevitably leads to defective materials, which lack long-range structural order. If defect-free functionalized monolayers are required, a radically new approach needs to be developed. Here we present a pre-synthetic method based on coordination chemistry that affords the isolatio…

chemistry.chemical_classificationchemistry.chemical_compoundMembraneMaterials scienceFerrocenechemistryLigandMonolayerMoleculeSurface modificationNanotechnologyPolymerCoordination complex
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Solid State NMR Structure Analysis of the Antimicrobial Peptide Gramicidin S in Lipid Membranes: Concentration-Dependent Re-alignment and Self-Assemb…

2008

Antimicrobial peptides can kill bacteria by permeabilizing their cell membrane, as these amphiphilicmolecules interact favourably with lipid bilayers. This mechanism of action is attributed eitherto the formation of a peptide “carpet” on the membrane surface, or to a transmembranepore. However, the structure of such a pore has not yet been resolved under relevant conditions.Gramicidin S is a symmetrical cyclic β-sheet decapeptide, which has been previouslyshown by solid state NMR to lie flat on the membrane surface at low peptide:lipid ratios (≤ 1:80).Using highly sensitive 19F-NMR, supported by 15N-labelling,we found that gramicidin S can flip into an upright transmembrane alignment at hig…

chemistry.chemical_classificationchemistry.chemical_compoundMembranechemistryPeripheral membrane proteinMembrane fluidityBiophysicsOrganic chemistryPeptideLipid bilayer phase behaviorGramicidin SModel lipid bilayerLipid bilayer
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1993

Several zwitterionic polymers were prepared by radical homopolymerization of surfactant monomers which bear diallyl, diene or vinylcyclopropane moieties. These polymer systems were complemented by alternating copolymers of appropriate zwitterionic vinyl compounds. Thus, polymers with reduced (as compared with simple vinylic homopolymers, or statistical copolymers) and well defined density of surfactant side groups are obtained. The solubilities found for these polymers are dominated by polymer geometry rather than by the balance of hydrophilic and hydrophobic fragments, thus corroborating a “main-chain spacer” model proposed recently. All water-soluble polymers exhibit characteristic featur…

chemistry.chemical_classificationchemistry.chemical_compoundMonomerDienePulmonary surfactantChemistryRadical polymerizationMonolayerPolymer chemistryCopolymerPolymerSolubilityDie Makromolekulare Chemie
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<title>Optically induced switching of dicyclohexylamino substituted azobenzene derivatives in thin ordered films</title>

2005

During the last years, there has been an increasing interest in the photoinduced switching effects. Among the objects of concern azobenzene derivatives, isomerizing under UV and visible light, occupy a prominent position. To understand the photoresponse of these materials in the condensed phase, their spectroscopic and electrical properties are studied. It is shown that the photoresponse depends on the orientation of the molecules and their packing. A number of novel azobenzene derivatives containing a N,N-dicyclohexyl sulfonamide moiety is synthesized. The derivatives differ in the length of alkyl chains between the azobenzene moiety and SH or COOH groups. The morphology and the photoinduc…

chemistry.chemical_classificationchemistry.chemical_compoundchemistryAzobenzenePhase (matter)MonolayerMoleculeMoietySelf-assembled monolayerPhotochemistryAlkylVisible spectrumSPIE Proceedings
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rac-1,1,1,6,6,6-Hexachlorohex-3-yne-2,5-diol hemihydrate

2017

The asymmetric unit of the title compound, C6H4Cl6O2·0.5H2O, contains one molecule of 1,1,1,6,6,6-hexachlorohex-3-yne-2,5-diol and half a water molecule located on a twofold rotation axis. In the crystal, pairs of hexachlorohexynediol molecules form centrosymmetric dimers connectedviapairwise O—H...O hydrogen bonds. These dimers are connected by water molecules, resulting in layers parallel to theabplane.

chemistry.chemical_classificationcrystal structurecentrosymmetric dimer010405 organic chemistryChemistryStereochemistryHydrogen bondHemihydrateDiolAlkynelayer structureCrystal structure010402 general chemistryHEXA01 natural sciences0104 chemical sciencesorganochlorine compoundCrystalCrystallographychemistry.chemical_compoundlcsh:QD901-999alkyneMoleculelcsh:CrystallographyIUCrData
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Heterogeneous salt distribution in hot snacks enhances saltiness without loss of acceptability

2013

clef UT: 000318667000026; International audience; Abstract Health issues have led worldwide organisations to encourage the food industry to reduce salt in processed foods. Therefore, different strategies for salt reduction have been investigated. Here, the effect of heterogeneous salt distribution on saltiness perception intensity was assessed to compensate for salt reduction in snack foods. Two models of hot-served baked foods were developed. One model is made of two layers that vary in composition (cream-based and cereal-based layers) and salt (NaCl) concentration; the other one is made of four cream-based layers that vary in salt concentrations. Consumer panels rated the saltiness intens…

chemistry.chemical_classificationlikingTasteFood industrybusiness.industryChemistry[ SDV.AEN ] Life Sciences [q-bio]/Food and Nutritiondigestive oral and skin physiologySalt reductionfood and beveragesSalt (chemistry)layered food productsSnack foodConsumer panelstaste enhancementFood processingheterogeneous tastant distributionFood sciencesalt reductionbusiness[SDV.AEN]Life Sciences [q-bio]/Food and NutritionFood ScienceFood Research International
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