Search results for "Molecules"

showing 10 items of 1147 documents

Immunoproteomic studies on paediatric opsoclonus-myoclonus associated with neuroblastoma

2016

We aimed to identify new cell-membrane antigens implicated in opsoclonus-myoclonus with neuroblastoma. The sera of 3 out of 14 patients showed IgG electron-microscopy immunogold reactivity on SH-SY5Y neuroblastoma cells. Immunoprecipitation experiments using rat brain synaptosomes and SH-SY5Y cells led to the identification of: (1) thirty-one nuclear/cytoplasmic proteins (including antigens HuB, HuC); (2) seven neuronal membrane proteins, including the Shaw-potassium channel Kv3.3 (KCNC3), whose genetic disruption in mice causes ataxia and generalized muscle twitching. Although cell-based assays did not demonstrate direct antigenicity, our findings point to Shaw-related subfamily of the pot…

Central Nervous SystemMale0301 basic medicineAntigenicityDatabases FactualThymomaImmunoprecipitationKCTD7Cell Adhesion Molecules NeuronalImmunologyNerve Tissue ProteinsBiologyNeuroblastoma03 medical and health sciences0302 clinical medicineAntigenCell Line TumorNeuroblastomaOpsoclonus myoclonus syndromemedicineAnimalsHumansImmunology and AllergyRats WistarChildOpsoclonus-Myoclonus SyndromeBrain NeoplasmsMembrane ProteinsNuclear ProteinsImmunogold labellingmedicine.diseaseMolecular biologyRatsHEK293 Cells030104 developmental biologyShaw Potassium ChannelsNeurologyMembrane proteinEncephalitisFemaleNeurology (clinical)030217 neurology & neurosurgerySynaptosomesJournal of Neuroimmunology
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The evolutionary history and tissue mapping of GPR123: specific CNS expression pattern predominantly in thalamic nuclei and regions containing large …

2007

The Adhesion family of G protein-coupled receptors (GPCRs) includes 33 receptors and is the second largest GPCR family. Most of these proteins are still orphans and fairly little is known of their tissue distribution and evolutionary context. We report the evolutionary history of the Adhesion family protein GPR123 as well as mapping of GPR123 mRNA expression in mouse and rat using in situ hybridization and real-time PCR, respectively. GPR123 was found to be well conserved within the vertebrate lineage, especially within the transmembrane regions and in the distal part of the cytoplasmic tail, containing a potential PDZ binding domain. The real-time PCR data indicates that GPR123 is predomin…

Central Nervous SystemMaleModels MolecularNeuronal signal transductionPDZ domainGene ExpressionContext (language use)In situ hybridizationBiologyBiochemistryReceptors G-Protein-CoupledMiceCellular and Molecular NeuroscienceAnimalsHumansTissue DistributionRNA MessengerNeural Cell Adhesion MoleculesIn Situ HybridizationPhylogenyG protein-coupled receptorReverse Transcriptase Polymerase Chain ReactionPyramidal CellsSubiculumRatsCell biologySignal transductionSequence AlignmentNeuroscienceBinding domainJournal of Neurochemistry
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The chemical bonds in CuH, Cu2, NiH, and Ni2 studied with multiconfigurational second order perturbation theory

1994

The performance of multiconfigurational second order perturbation theory has been analyzed for the description of the bonding in CuH, Cu2, NiH, and Ni2. Large basis sets based on atomic natural orbitals (ANOS) were employed. The effects of enlarging the active space and including the core‐valence correlation contributions have also been analyzed. Spectroscopic constants have been computed for the corresponding ground state. The Ni2 molecule has been found to have a 0+g ground state with a computed dissociation energy of 2.10 eV, exp. 2.09 eV, and a bond distance of 2.23 Å. The dipole moments of NiH and CuH are computed to be 2.34 (exp. 2.4±0.1) and 2.66 D, respectively. pou@uv.es ; merchan@…

Chemical BondsGeneral Physics and AstronomyDissociation EnergyDipole MomentsPerturbation Theory ; Chemical Bonds ; Configuration Interaction ; Copper Hydrides ; Nickel Hydrides ; Copper ; Nickel ; Electron Correlation ; Core Levels ; Dissociation Energy ; Dipole Moments ; Bond Lengths ; Diatomic MoleculesCore LevelsBond LengthsNickelPhysical and Theoretical ChemistryPerturbation theory:FÍSICA::Química física [UNESCO]Nickel HydridesDiatomic MoleculesElectronic correlationChemistryConfiguration interactionBond-dissociation energyDiatomic moleculeUNESCO::FÍSICA::Química físicaBond lengthConfiguration InteractionChemical bondCopper HydridesPerturbation TheoryElectron CorrelationAtomic physicsGround stateCopper
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Coupled-cluster theory for atoms and molecules in strong magnetic fields

2015

An implementation of coupled-cluster (CC) theory to treat atoms and molecules in finite magnetic fields is presented. The main challenges for the implementation stem from the magnetic-field dependence in the Hamiltonian, or, more precisely, the appearance of the angular momentum operator, due to which the wave function becomes complex and which introduces a gauge-origin dependence. For this reason, an implementation of a complex CC code is required together with the use of gauge-including atomic orbitals to ensure gauge-origin independence. Results of coupled-cluster singles-doubles-perturbative-triples (CCSD(T)) calculations are presented for atoms and molecules with a focus on the depende…

Chemical Physics (physics.chem-ph)Physics010304 chemical physicsAtoms in moleculesBinding energyFOS: Physical sciencesGeneral Physics and Astronomy01 natural sciencesMagnetic fieldsymbols.namesakeCoupled clusterAtomic orbitalPhysics - Chemical Physics0103 physical sciencessymbolsPhysical and Theoretical ChemistryAtomic physicsAngular momentum operator010306 general physicsHamiltonian (quantum mechanics)The Journal of Chemical Physics
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HfF+ as a candidate to search for the nuclear weak quadrupole moment

2018

Nuclei with a quadrupole deformation, such as $^{177}\mathrm{Hf}$ have enhanced weak quadrupole moment which induces the tensor weak electron-nucleus interaction in atoms and molecules. Corresponding parity-non-conserving (PNC) effect is strongly enhanced in the ${}^{3}{\mathrm{\ensuremath{\Delta}}}_{1}$ electronic state of the $^{177}\mathrm{HfF}^{+}$ cation which has very close opposite parity levels mixed by this tensor interaction. In the present paper we perform relativistic many-body calculations of this PNC effect. It is shown that the tensor weak interaction induced by the weak quadrupole moment gives the dominating contribution to the PNC effects in $^{177}\mathrm{HfF}^{+}$ which s…

Chemical Physics (physics.chem-ph)PhysicsAtomic Physics (physics.atom-ph)Nuclear TheoryAtoms in moleculesFOS: Physical sciencesParity (physics)Weak interaction01 natural sciencesPhysics - Atomic Physics010305 fluids & plasmasPhysics - Chemical Physics0103 physical sciencesQuadrupoleNeutronPhysics::Atomic PhysicsAtomic physics010306 general physicsPhysical Review A
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Computer simulation of bottle-brush polymers with flexible backbone: good solvent versus theta solvent conditions.

2011

By Molecular Dynamics simulation of a coarse-grained bead-spring type model for a cylindrical molecular brush with a backbone chain of $N_b$ effective monomers to which with grafting density $\sigma$ side chains with $N$ effective monomers are tethered, several characteristic length scales are studied for variable solvent quality. Side chain lengths are in the range $5 \le N \le 40$, backbone chain lengths are in the range $50 \le N_b \le 200$, and we perform a comparison to results for the bond fluctuation model on the simple cubic lattice (for which much longer chains are accessible, $N_b \le 1027$, and which corresponds to an athermal, very good, solvent). We obtain linear dimensions of …

Chemical Physics (physics.chem-ph)chemistry.chemical_classificationQuantitative Biology::BiomoleculesMaterials scienceCharacteristic lengthTheta solventFOS: Physical sciencesGeneral Physics and AstronomyBackbone chainPolymerCondensed Matter - Soft Condensed MatterPower lawCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundMolecular dynamicschemistryChemical physicsPhysics - Chemical PhysicsSide chainSoft Condensed Matter (cond-mat.soft)Physical and Theoretical ChemistrySolvent effectsThe Journal of chemical physics
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Exploring Chemical Reactivity in Enzyme Catalyzed Processes Using QM/MM Methods: An Application to Dihydrofolate Reductase

2015

Enzymes are the catalysts used by living organisms to accelerate chemical processes under physiological conditions. In this chapter, we illustrate the current view about the origin of their extraordinary rate enhancement based on molecular simulations and, in particular, on methods based on the combination of Quantum Mechanics and Molecular Mechanics potentials which provide a solution to treat the chemical reactivity of these large and complex molecular systems. Computational studies on Dihydrofolate Reductase have been selected as a conductor wire to present the evolution and difficulties to model chemical reactivity in enzymes. The results discussed here show that experimental observatio…

Chemical processQuantitative Biology::BiomoleculesbiologyChemistryProtein dynamicsMolecular mechanicsEnzyme catalysisQM/MMTransition state theoryMolecular dynamicsBiochemistryChemical physicsDihydrofolate reductasebiology.protein
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Nanostructuring Biopolymers for Improved Food Quality and Safety

2018

Abstract Food-grade biopolymers, apart from their inherent nutritional properties, can be tailored designed for improving food quality and safety, either serving as delivery vehicles for bioactive molecules, or as novel packaging components, not only improving the transport properties of biobased packaging structures, but also imparting active antibacterial and antiviral properties. In this chapter, the potential of different food-grade biopolymers (mainly proteins and carbohydrates but also some biopolyesters) to serve as encapsulating matrices for the protection of sensitive bioactives or as nanostructured packaging layers to improve transport properties and control the growth of pathogen…

ChemistryBioactive moleculesNanotechnologyPathogenic bacteria04 agricultural and veterinary sciencesAntimicrobialmedicine.disease_cause040401 food science03 medical and health sciences0404 agricultural biotechnology0302 clinical medicineFunctional food030221 ophthalmology & optometrymedicineFood quality
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Understanding the local reactivity in polar organic reactions through electrophilic and nucleophilic Parr functions

2013

[EN] Building upon our recent studies devoted to the bonding changes in polar reactions [RSC Advances, 2012, 2, 1334 and Org. Biomol. Chem., 2012, 10, 3841], we propose herein two new electrophilic, P-k(+), and nucleophilic, P-k(-), Parr functions based on the spin density distribution at the radical anion and at the radical cation of a neutral molecule. These local functions allow for the characterisation of the most electrophilic and nucleophilic centres of molecules, and for the establishment of the regio- and chemoselectivity in polar reactions. The proposed Parr functions are compared with both, the Parr-Yang Fukui functions [J. Am. Chem. Soc. 1984, 106, 4049] based on frontier molecul…

ChemistryGeneral Chemical EngineeringExchangeGeneral ChemistryMoleculesDFTBond-formationDensittyIndexNucleophileRadical ionOrganic reactionComputational chemistryDiels-alder reactionElf analysisElectrophileLocalization functionMolecular orbitalChemoselectivityMulliken population analysis13-DipolarDiels–Alder reaction
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Dimeric resorcinarene salt capsules with very tight encapsulation of anions and guest molecules

2015

Crystallization of N-cyclohexyl ammonium resorcinarene triflate from methanol results in a dimeric capsule capable of trapping two triflate anions and two methanol molecules within a 341 A3 cavity while with 1,4-dioxane as a guest it forms a new larger dimeric capsule with volume of 679 A3 encapsulating four 1,4-dioxane and four water molecules, resulting in packing coefficients of 0.75 and 0.67, respectively.

ChemistryGeneral Chemical EngineeringInorganic chemistrydimeric capsulesGeneral ChemistryResorcinarenelaw.inventionguest moleculeschemistry.chemical_compoundlawPolymer chemistryMoleculeMethanolCrystallizationta116anionsTrifluoromethanesulfonateRSC Advances
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