Search results for "Self-Assembly"

showing 10 items of 438 documents

Hepatitis B core particles as a universal display model: a structure-function basis for development

1999

AbstractBecause it exhibits a remarkable capability to accept mutational intervention and undergo correct folding and self-assembly in all viable prokaryotic and eukaryotic expression systems, hepatitis B core (HBc) protein has been favored over other proposed particulate carriers. Structurally, the unusual α-helical organization of HBc dimeric units allows introduction of foreign peptide sequences into several areas of HBc shells, including their most protruding spikes. Progress toward full resolution of the spatial structure as well as accumulation of chimeric HBc-based structures has brought closer the knowledge-based design of future vaccines, gene therapy tools and other artificial par…

Hepatitis B virusGenes ViralCryo-electron microscopyMacromolecular SubstancesProtein ConformationBiophysicsComputational biologyBiologyBiochemistryMolecular displayEpitopesProtein structureStructural BiologyGeneticsProkaryotic expressionAnimalsHumansMolecular BiologyDrug CarriersBinding SitesSpatial structureViral Core ProteinsStructure functionHepatitis B core proteinvirus diseasesCell BiologyBasis (universal algebra)Self-assemblyAntigenicityVirologyBiological EvolutionHepatitis B Core Antigensdigestive system diseasesFolding (chemistry)Protein structureElectron cryomicroscopyDimerizationHepatitis b coreFEBS Letters
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Exploring the Interplay Between Ligand Derivatisation and Cation Type in the Assembly of Hybrid Polyoxometalate Mn-Andersons

2012

Herein a library of hybrid Mn-Anderson polyoxometalates anions are presented: 1, [(MnMo6 O18 )((OCH2 )3 -C-(CH2 )7 CHCH2 )2 ](3-) ; compound 2, [(MnMo6 O18 )((OCH2 )3 C-NHCH2 C16 H9 )2 ](3-) ; compound 3, [(MnMo6 O18 )((OCH2 )3 C-(CH2 )7 CHCH2 )1 ((OCH2 )3 C-NHCH2 C16 H9 )1 ](3-) ; compound 4, [(MnMo6 O18 )((OCH2 )3 C-NHC(O)CH2 CHCH2 )2 ](3-) and compounds 5-9, [(MnMo6 O18 )((OCH2 )3 C-NHC(O)(CH2 )x CH3 )2 ]), where x = 4, 10, 12, 14, and 18 respectively. The compounds resulting from the cation exchange of the anions 1-9 to give TBA (a) and DMDOA (b) salts, and additionally for compounds 1, 2 and 3, tetraphenylphosphonium (PPh4 ) (c) salts, are explored at the air/water interface using scan…

Hexagonal crystal systemChemistryLigandStereochemistrySupramolecular chemistryGeneral Chemistrypolyoxometalate AFM self-assembly thin filmsBiomaterialsCrystallographyCovalent bondPolyoxometalateGeneral Materials ScienceScanning Force MicroscopyBiotechnologySmall
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Reversible Supracolloidal Self-Assembly of Cobalt Nanoparticles to Hollow Capsids and Their Superstructures

2017

| openaire: EC/FP7/291364/EU//MIMEFUN The synthesis and spontaneous, reversible supracolloidal hydrogen bond-driven self-assembly of cobalt nanoparticles (CoNPs) into hollow shell-like capsids and their directed assembly to higher order superstructures is presented. CoNPs and capsids form in one step upon mixing dicobalt octacarbonyl (Co2CO8) and p-aminobenzoic acid (pABA) in 1,2-dichlorobenzene using heating-up synthesis without additional catalysts or stabilizers. This leads to pABA capped CoNPs (core ca. 5nm) with a narrow size distribution. They spontaneously assemble into tunable spherical capsids (d≈50-200nm) with a few-layered shells, as driven by inter-nanoparticle hydrogen bonds th…

Hydrogen bondingta221Nanoparticlechemistry.chemical_element02 engineering and technology010402 general chemistry01 natural sciencesCatalysischemistry.chemical_compoundColloidCapsidsDicobalt octacarbonylta116ta114ChemistryHydrogen bondColloidal self-assemblyGeneral ChemistryGeneral Medicine021001 nanoscience & nanotechnology0104 chemical sciencesSolventCrystallographyElectron tomographycobalt nanoparticlesMagnetic nanoparticlesnanoparticlesSelf-assembly0210 nano-technologyCobaltSuperparamagnetismAngewandte Chemie
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Capturing Hydrophobic Trifluoroiodomethane in Water into an M 4 L 6 Cage

2016

Synthetically important trifluoroiodomethane (CF3I) was trapped in water by using a metal–organic supramolecular anionic cage. Under ambient conditions, nearly 1:1 encapsulation of the hydrophobic, gaseous CF3I substrate with the cage was observed, and its binding constant was calculated by relative comparison with benzene encapsulation.

Hydrophobic Trifluoroiodomethane010405 organic chemistrywaterSupramolecular chemistrychemistry010402 general chemistryPhotochemistry01 natural sciencesBinding constant0104 chemical sciencesCondensed Matter::Soft Condensed MatterInorganic ChemistryHydrophobic effectmetal–organic frameworkschemistry.chemical_compoundchemistryPhysics::Atomic and Molecular ClustersTrifluoroiodomethaneSelf-assemblyPhysics::Chemical PhysicsBenzeneCageHost–guest chemistryta116European Journal of Inorganic Chemistry
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Raman study of self-assembled InAs/InP quantum wire stacks with varying spacer thickness

2008

http://link.aip.org/link/?JAPIAU/104/033523/1

III-V semiconductorsMaterials sciencePhononAnnealing (metallurgy)General Physics and AstronomyCritical pointsDielectricAnnealingCondensed Matter::Materials Sciencesymbols.namesake:FÍSICA [UNESCO]Indium compoundsCondensed matter physicsQuantum wireUNESCO::FÍSICAAnnealing ; Critical points ; III-V semiconductors ; Indium compounds ; Phonons ; Raman spectra ; Self-assembly ; Semiconductor quantum wiresSelf-assemblyCondensed Matter::Mesoscopic Systems and Quantum Hall EffectMolecular vibrationSemiconductor quantum wiressymbolsPhononsRaman spectraRaman spectroscopyExcitationRaman scatteringJournal of Applied Physics
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Oscillator strength reduction induced by external electric fields in self-assembled quantum dots and rings

2007

We have carried out continuous wave and time resolved photoluminescence experiments in self-assembled In(Ga)As quantum dots and quantum rings embedded in field effect structure devices. In both kinds of nanostructures, we find a noticeable increase of the exciton radiative lifetime with the external voltage bias that must be attributed to the field-induced polarizability of the confined electron hole pair. The interplay between the exciton radiative recombination and the electronic carrier tunneling in the presence of a stationary electric field is therefore investigated and compared with a numerical calculation based on the effective mass approximation.

III-V semiconductorsOscillator strengthRadiative lifetimesTime resolved spectraTunnellingSelf assembledCondensed Matter::Materials ScienceGallium arsenideIndium compoundsElectric fieldQuantum mechanicsSemiconductor quantum dotsNetwork of excellenceEuropean commissionPhotoluminescenceQuantum tunnellingPhysicsSelf-assemblyCondensed Matter::Mesoscopic Systems and Quantum Hall EffectCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsQuantum dotEffective massElectron hole recombinationElectron-hole recombinationPhysical Review B
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Mutilation of RNA phage Qβ virus-like particles: from icosahedrons to rods

2000

Icosahedral virus-like particles (VLPs) of RNA phage Qbeta are stabilized by four disulfide bonds of cysteine residues 74 and 80 within the loop between beta-strands F and G (FG loop) of the monomeric subunits, which determine the five-fold and quasi-six-fold symmetry contacts of the VLPs. In order to reduce the stability of Qbeta VLPs, we mutationally converted the amino acid stretch 76-ANGSCD-81 within the FG loop into the 76-VGGVEL-81 sequence. It led to production in Escherichia coli cells of aberrant rod-like Qbeta VLPs, along with normal icosahedral capsids. The length of the rod-like particles exceeded 4-30 times the diameter of icosahedral Qbeta VLPs.

Icosahedral symmetryvirusesGenetic VectorsMolecular Sequence DataBiophysicsBiologymedicine.disease_causecomplex mixturesBiochemistryVirus-like particleStructural BiologyGeneticsmedicineAmino Acid SequenceCysteineMolecular BiologyEscherichia coliPeptide sequenceIcosahedronAlloleviviruschemistry.chemical_classificationSequence Homology Amino AcidRod-like structureVirionvirus diseasesRNASelf-assemblyCell Biologybiochemical phenomena metabolism and nutritionAmino acidCrystallographyCapsidchemistryMutagenesis Site-DirectedRNA ViralRNA phage QβVirus-like particleCysteineFEBS Letters
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Polymer/metal hybrid multilayers modified Schottky devices

2013

Insulating, polymethylmethacrylate (PMMA), and semiconducting, poly(3-hexylthiophene) (P3HT), nanometer thick polymers/Au nanoparticles based hybrid multilayers (HyMLs) were fabricated on p-Si single-crystal substrate. An iterative method, which involves, respectively, spin-coating (PMMA and P3HT deposition) and sputtering (Au nanoparticles deposition) techniques to prepare Au/HyMLs/p-Si Schottky device, was used. The barrier height and the ideality factor of the Au/HyMLs/p-Si Schottky devices were investigated by current-voltage measurements in the thickness range of 1-5 bilayers. It was observed that the barrier height of such hybrid layered systems can be tuned as a function of bilayers …

Ideality factorMaterials sciencePhysics and Astronomy (miscellaneous)Layered systemNanoparticleSilicon GoldNanotechnologySingle-crystal substrates DepositionSubstrate (electronics)Poly-3-hexylthiopheneSettore ING-INF/01 - ElettronicaSettore FIS/03 - Fisica Della MateriaNanoparticleSputteringPolymer; Au nanoparticles; Schottky devicePolymerHybrid multilayerConductive polymerSpin coatingbusiness.industryBarrier heightSchottky diodeSputter depositionCurrent-voltage measurementSemiconducting siliconSchottky deviceOptoelectronicsSelf-assemblybusinessAu nanoparticles
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One‐pot synthesis of [2+2]‐helicate‐like macrocycle and 2+4‐μ 4 ‐oxo tetranuclear open frame complexes: Chiroptical properties and asymmetric oxidati…

2020

Inorganic Chemistry010405 organic chemistryChemistryPolymer chemistryFrame (networking)One-pot synthesisOxidative coupling of methaneGeneral ChemistrySelf-assembly010402 general chemistry01 natural sciences0104 chemical sciencesApplied Organometallic Chemistry
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Self-assembly of a M4L6 complex with unexpected S4 symmetry

2014

In a one-pot reaction 1,4-diaminobenzene and 2-formylpyridine, as the reacting subcomponents, self-assemble to a small supramolecular M4L6 pseudo-tetrahedron with unexpected S4 symmetry in the presence of Fe(ii) ions.

Inorganic ChemistryCrystallography010405 organic chemistryChemistryLigandSelf-assemblySymmetry (geometry)010402 general chemistryta11601 natural sciences3. Good health0104 chemical sciencesIonDalton Trans.
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