Search results for "Complex."

showing 10 items of 5824 documents

Purification of Large Cytosolic Proteases for In Vitro Assays: 20S and 26S Proteasomes

2012

Proteasomes are the main cytosolic proteases responsible for generating peptides for antigen processing and presentation in the MHC (major histocompatibility complex) class-I pathway. Purified 20S and 26S proteasomes have been widely used to study both specificity and efficiency of antigen processing. Here, we describe the purification of active human 20S and 26S proteasomes from human erythrocytes by DEAE-ion exchange chromatography, ammonium sulfate precipitation, glycerol density gradient centrifugation, and Superose-6 size exclusion chromatography and their characterization using fluorogenic substrates and specific inhibitors.

Differential centrifugationCytosolProteasesProteasomebiologyBiochemistryAntigen processingChemistrybiology.proteinMajor histocompatibility complexPolyacrylamide gel electrophoresisAmmonium sulfate precipitation
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Nuclear DNA fractions with grossly different base ratios in the genome of the marine sponge Geodia cydonium

2008

The DNA of the marine sponge Geodia cydonium (G.c.), a member of the phylogenetically old phylum Porifera, was characterized by density gradient centrifugation and by determining its genetic complexity by reassociation kinetics. At least five subcomponents were identified by curve-fit analyses of analytical density gradient centrifugation profiles of total G.c.-DNA. Four of these subcomponents were isolated from total G.c.-DNA by preparative density gradient centrifugation. The GC-contents of the subcomponents were determined to be 36.4%, 44.0%, 58.7%, and 66.1%, respectively. To our knowledge, such an extreme heterogeneity of DNA composition has never before been observed for any organism.…

Differential centrifugationchemistry.chemical_classificationGenetic complexityBase (chemistry)Geodia cydoniumBiologybiology.organism_classificationGenomeNuclear DNASpongechemistry.chemical_compoundBiochemistrychemistryBotanyDNA
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Time multiplexing super-resolved imaging without a priori knowledge of the spatial distribution of the encoding structured illumination

2021

Time multiplexing is a super-resolution technique that sacrifices time to overcome the resolution reduction obtained because of diffraction. There are many super resolution methods based on time multiplexing, but all of them require a priori knowledge of the time changing encoding mask, which is projected on the object and used to encode and decode the high-resolution information. In this paper, we present a time multiplexing technique that does not require the a priori knowledge on the projected encoding mask. First, the theoretical concept of the technique is demonstrated; then, numerical simulations and experimental results are presented.

DiffractionComputer sciencebusiness.industryResolution (electron density)02 engineering and technology021001 nanoscience & nanotechnology01 natural sciencesMultiplexingAtomic and Molecular Physics and Optics010309 opticsReduction (complexity)OpticsEncoding (memory)0103 physical sciencesA priori and a posteriori0210 nano-technologybusinessImage resolutionAlgorithmComputer Science::Information TheoryOptics Express
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Mixed valence mono- and hetero-metallic grid catenanes

2015

Multicomponent self-assembly was employed to obtain, in the solid state, a series of mixed valence mono- and hetero-metallic grid catenanes, which were characterized by single crystal X-ray diffraction.

DiffractionValence (chemistry)ChemistryCatenanestructural complexityPhysics::OpticsGeneral ChemistryGrid3. Good healthMetalCondensed Matter::Materials ScienceChemistryCatenationCrystallographycatenanesvisual_artvisual_art.visual_art_mediumCondensed Matter::Strongly Correlated Electronsta116Single crystal
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Editorial of Critical Phenomena and Diffusion in Complex Systems

2008

Diffusion in Complex Systems
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Different Sorption Behaviors for Wine Polyphenols in Contact with Oak Wood

2007

The evolution of polyphenols of enological interest- monomeric anthocyanins, (+)-catechin, (-)-epicatechin, gallic acid, and trans-resveratrol-in the presence of oak wood was investigated in aging-model conditions. Disappearance kinetics showed that, except for gallic acid, all of the wine polyphenols tend to disappear from the model wine in presence of oak wood, to reach an equilibrium after 20 days of contact. At equilibrium, the higher disappearance rates were obtained for monomeric anthocyanins and trans-resveratrol with values of 20 and 50%, respectively. For monomeric anthocyanins, the rate of disappearance seemed to be independent of their nature. In order to evaluate the contributio…

DiffusionKineticsSorption kineticsWinecomplex mixturesAnthocyaninschemistry.chemical_compoundQuercusGlucosidesPhenolsBotanyStilbenesGallic acidWineFlavonoidsChemistryExtraction (chemistry)food and beveragesPolyphenolsSorptionGeneral ChemistryWoodKineticsPolyphenolResveratrolEnvironmental chemistryAdsorptionGeneral Agricultural and Biological Sciences
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Impact of the community structure on the dynamics of complex networks

2023

Networks are everywhere. We encounter them daily in our lives, through our social interactions, how we come up with decisions in our brain, to having phone calls, conducting financial transactions, and traveling from one place to another. Individual actions are influenced by their environment, which is, in turn, influenced by the network's topology. Notably, individuals may change their actions, ideas, or opinions to conform to the aspirations of a particular social group. In the same vein, the spread of a virus can take a certain course if the network's structure induces specific pathways for expansion. In such scenarios, communities substantially impact the evolution of the dynamics. They…

Diffusion[INFO.INFO-NI] Computer Science [cs]/Networking and Internet Architecture [cs.NI]CommunautésRéseaux complexesCommunitiesComplex networksCentralityCentralitéTopologieInfluential nodesTopologyNœuds influents
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A polymeric two-dimensional mixed-metal network. Crystal structure and magnetic properties of {[P(Ph)4][MnCr(ox)3]}

1994

Abstract The mixed-metal ferromagnet {[P(Ph) 4 ][MnCr(ox) 3 ]} n , where Ph is phenyl and ox is oxalate, has been prepared and a two-dimensional network structure, extended by Mn(II)-ox-Cr(III) bridges, has been determined from single crystal X-ray data. Crystal data: space group R 3 c , a = b =18.783(3), c =57.283(24) A, α=β=90, γ=120°, Z =24 (C 30 H 20 O 12 PCrMn). The magnetic susceptibility data obey the Curie-Weiss law in the temperature range 260–20 K with a positive Weiss constant of 10.5 K. The temperature dependence of the molar magnetization exhibits a magnetic phase transition at T c =5.9 K. The structure is discussed in relation to the strategy for preparing molecular based ferr…

Dinuclear complexesChemistryStereochemistryMagnetismMagnetismCrystal structureAtmospheric temperature rangeMagnetic susceptibilityInorganic ChemistryMagnetizationCrystallographyChromium complexesFerromagnetismddc:540Crystal structuresX-ray crystallographyMaterials ChemistryPhysical and Theoretical ChemistrySingle crystalManganese complexesInorganica Chimica Acta
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Antiferromagnetic Interactions in Copper(II) µ-Oxalato Dinuclear Complexes: The Role of the Counterion

2018

We report the preparation, crystal structure determination, magnetic properties and DFT calculations of five oxalato-bridged dicopper(II) complexes of formula [Cu-2(bpy)(2-)(H2O)(2)(C2O4)](CF3SO3)(2) (1), [Cu-2(bpy)(2)(C2O4)](PF6)(2) (2), [Cu-2(bpy)(2)(C2O4)](ClO4)(2) (3), [Cu-2(bpy)(2)Cl-2(C2O4)]center dot H2O (4) and [Cu-2(bpy)(2)(NO2)(2)(C2O4)] (5) (bpy = 2,2'-bipyridine and C2O42-= oxalate). Compounds 1, 2, 4 and 5 crystallize in the monoclinic system and 3 crystallizes in the triclinic system. The oxalate ligands in 1-5 adopt the bis-bidentate coordination mode and the two bpy molecules act as terminal ligands. The coordination of the counterions and the surroundings of the copper(II) …

Dinuclear complexesMatériauxFerromagnetismechemistry.chemical_elementCrystal structure[CHIM.INOR]Chemical Sciences/Inorganic chemistryTriclinic crystal system010402 general chemistry01 natural sciencesOxalateInorganic Chemistrychemistry.chemical_compoundOxalatoMagnetic propertiesAntiferromagnetismMolecule[CHIM.COOR]Chemical Sciences/Coordination chemistryGénie des procédéschemistry.chemical_classificationCoure010405 organic chemistryPropietats magnètiquesCopper0104 chemical sciences3. Good healthCrystallographyDensity functional calculationschemistryFerromagnetismCounterionCopperMonoclinic crystal system
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Complexes of diorganotin(IV) with aminoacids and a dipeptide. Synthesis and structural investigations.

2008

The aim of this work is to synthesize complexes of Arginine, effector of recognition, with organotin(IV) ions (R2Sn2+, R =Me, nBu) which are known to possess antitumour, antimicrobial, anti-inflammatory activities. The complexes were investigated by FT-IR and 119Sn Můssbauer.While identical stoichiometries are present for Me2Sn(Arg)2 and Me2Sn(Boc-Arg)2 complexes, 119Sn Můssbauer spectra give a clear evidence of different coordination modes. L-Arginine appears to behave as a chelating ligand through carboxylate and a-NH2 groups in the former, while in Nα-Boc-L-Arginine complex, the Nα-protected amino group being exempted from coordination, only the carboxylate groups are effectors of bondin…

Diorganotin (IV) complexes aminoacids and dipeptideSettore CHIM/03 - Chimica Generale E Inorganica
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