Search results for "HIF"

showing 10 items of 1515 documents

Analysis of expression of an alternative La (SS-B) cDNA and localization of the encoded N- and C-terminal peptides

1997

AbstractA deletion of an (A)-residue was detected in a cDNA encoding for the nuclear autoantigen La/SS-B. The cDNA was recently isolated from a cDNA library made from peripheral blood lymphocytes of a patient with primary Sjögren's Syndrome. The region, where the deletion occurred, represents a hot spot region in the La gene(s). It leads to a frame shift mutation and a premature stop codon eleven amino acids downstream of the deletion site within one of the protease sensitive regions of the La protein. In spite of the frame shift mutation expression of full length La protein occurred efficiently in E. coli. Full length La protein was also made in SF9 cells infected with recombinant baculovi…

DNA ComplementaryMolecular Sequence DataBiologyAutoantigensCell LineFrameshift mutationSingle-stranded binding proteinComplementary DNAEscherichia coliConsensus sequenceProtein biosynthesisHumansAmino Acid SequenceGeneMolecular BiologyBase SequencecDNA libraryCell BiologyMolecular biologyPeptide FragmentsSjogren's SyndromeRibonucleoproteinsCytoplasmMutationbiology.proteinBaculoviridaeGene DeletionBiochimica et Biophysica Acta (BBA) - Molecular Cell Research
researchProduct

Polarization-domain-wall complexes in fiber lasers

2013

To study the possible build-up of polarization-domain-walls (PDWs) in fiber laser cavities, an erbium-doped fiber ring laser was used and a wide range of vector polarization dynamics that can be selected at a given pump power, by using the degrees of freedom of two intracavity polarization controllers (PC) was investigated. A simple theoretical model that explains polarization switching in fiber ring lasers featuring a normally dispersive cavity with a typical, moderate, level of birefringence is presented. Such polarization dynamics, based on a special class of polarization-domain-wall structures, agrees qualitatively well with experimental observations. The paper stresses on the complex a…

DYNAMICSMaterials scienceChaoticPhysics::OpticsPolarization-maintaining optical fiberGraded-index fiber01 natural sciencesMolecular physicslaw.invention010309 opticsMEDIADouble-clad fiberOpticslawFiber laser0103 physical sciencesDispersion-shifted fiber010306 general physicsCircular polarizationRING LASER[PHYS.PHYS.PHYS-OPTICS]Physics [physics]/Physics [physics]/Optics [physics.optics]Polarization rotatorBirefringence[ PHYS.PHYS.PHYS-OPTICS ] Physics [physics]/Physics [physics]/Optics [physics.optics]Computer simulationbusiness.industrySingle-mode optical fiberStatistical and Nonlinear PhysicsLaserPolarization (waves)Atomic and Molecular Physics and OpticsSOLITONSbusinessring laser dynamics solitonsPhotonic-crystal fiber
researchProduct

Structure of SNX9 SH3 in complex with a viral ligand reveals the molecular basis of its unique specificity for alanine-containing class I SH3 motifs

2021

Class I SH3 domain-binding motifs generally comply with the consensus sequence [R/K]x0PxxP, the hydrophobic residue 0 being proline or leucine. We have studied the unusual 0 = Ala-specificity of SNX9 SH3 by determining its complex structure with a peptide present in eastern equine encephalitis virus (EEEV) nsP3. The structure revealed the length and composition of the n-Src loop as important factors determining specificity. We also compared the affinities of EEEV nsP3 peptide, its mutants, and cellular ligands to SNX9 SH3. These data suggest that nsP3 has evolved to minimize reduction of conformational entropy upon binding, hence acquiring stronger affinity, enabling takeover of SNX9. The R…

DYNAMICSPROLINE-RICH PEPTIDESviruksetPROTEINSvirusesHTLV-1 GagLigandsEVOLUTIONARY CONSERVATIONalfaviruksetsrc Homology DomainsHIGH-AFFINITYretroviruksetDOMAINStructural BiologyBINDINGAnimalsHorsesMolecular Biologysoluviestintä11832 Microbiology and virologyAlanineBinding SitesPXXP MOTIFSisothermal titration calorimetrySH3solution NMR spectroscopyEEEV nsP3HIV-11182 Biochemistry cell and molecular biologyproteiinitCHEMICAL-SHIFTS3111 BiomedicinePeptidesSNX9Protein Binding
researchProduct

First demonstration of active plasmonic device in true data traffic conditions: On/off thermo-optic modulation using a hybrid silicon-plasmonic asymm…

2012

We demonstrate the first system-level evaluation of an active plasmonic device in 10Gb/s data traffic conditions. Thermo-optic ON/OFF modulation with 3μs response time and 10mW power consumption is presented using an asymmetric MZI silicon-plasmonic gate.

Data trafficMaterials scienceSiliconbusiness.industrychemistry.chemical_elementSilicon on insulatorResponse timeAmplitude-shift keyingOpticschemistryPower consumptionModulationOptoelectronicsbusinessPlasmon
researchProduct

NMR chemical shift calculations within local correlation methods: the GIAO-LMP2 approach

2000

A scheme for the calculation of NMR chemical shifts using local second-order Moller–Plesset (LMP2) perturbation theory together with gauge-including atomic orbitals (GIAOs) is presented. Test calculations on the basis of a preliminary implementation within a conventional GIAO-MP2 code show that the deviations between GIAO-LMP2 and GIAO-MP2 are small, e.g., for 13C typically less than 1 ppm, and that the GIAO-LMP2 approach holds great promise for application to larger molecules.

Density matrixAtomic orbitalBasis (linear algebra)ChemistryComputational chemistryChemical shiftGeneral Physics and AstronomyMoleculeCorrelation methodPhysical and Theoretical ChemistryPerturbation theoryMolecular physicsPhysical Chemistry Chemical Physics
researchProduct

Theoretical study of isomerism in phenoxyimine-based precursors of coordinative olefin polymerization catalysts

2010

Precursors of post-metallocene olefin polymerization catalysts, unlike their predecessors, are usually octahedral transition metal complexes with multidentate ligands. Such ligands may wrap around the central atom in many ways, thus yielding several isomeric species. For a wide range of phenoxyimine (FI) ligands with different substituents, all the theoretically predicted diastereomers of group 4 and 5 complexes are available synthetically. However, only one of the isomers is usually preferred, and this is determined by the nature of the substituents in the FI ligand. The origin and mechanism of such preference has not been completely elucidated. We attempted to describe it quantitatively o…

DenticitySchiff baseLigandStereochemistryProcess Chemistry and TechnologyFI catalystSubstituentDiastereomerDFTCatalysisphenoxyimineCatalysischemistry.chemical_compoundchemistryTransition metalPolymer chemistryDensity functional theoryPhysical and Theoretical Chemistryolefin polymerizationJournal of Molecular Catalysis A-Chemical
researchProduct

A ferromagnetically coupled single hydroxido bridged tetranuclear nickel(II) Schiff base complex incorporating a Ni4O4 cubane core: Crystal structure…

2013

Abstract The new tetranuclear nickel(II) complex [Ni4(OH)(L)(HL)2(CH3OH)1.5(H2O)1.5]·9H2O (1) has been synthesised by the reaction of NiCl2·6H2O and the Schiff base ligand H3L (H3L = (CH3O)(OH)C6H3CH N–C(CH3)(CH2OH)2), prepared by the 1:1 condensation of 2-amino-2-methyl-1,3-propanediol and o-vanillin, and characterized by different physicochemical methods. Single crystal X-ray structural determination identifies a Ni4O4 cubane moiety as the central part of the complex unit. The presence of a single μ3-hydroxido bridged oxygen occupying only one vertex of the Ni4O4 cubane core is rare in Ni4O4 cubanes (ca. 5% of occurrence). Structural analysis also reveals two similar alkoxido oxygen atoms…

DenticitySchiff baseStereochemistryLigandchemistry.chemical_elementCrystal structureInorganic Chemistrychemistry.chemical_compoundNickelCrystallographychemistryOctahedronCubaneMaterials ChemistryPhysical and Theoretical ChemistrySingle crystalPolyhedron
researchProduct

A dinuclear rhodium(III) complex with the N,N′-ethylenebis(salicylideneiminato) (salen) ligand in a bridging bis-bidentate mode of coordination. Crys…

1990

In this communication we describe the synthesis and crystal structure of the complex [{Rh(η 2 -(C 6 H 4 )PPh 2 )(η 2 -P(o-ClC 6 H 4 )Ph 2 )} 2 (salen)]-(SbF 6 ) 2 , showing the bridging configuration of the salen ligand

DenticitySchiff baseStereochemistrychemistry.chemical_elementCrystal structureRhodiumInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryMetal salen complexesSalen ligandX-ray crystallographyMaterials ChemistryMoleculePhysical and Theoretical ChemistryInorganica Chimica Acta
researchProduct

Co-existence of ferro- and antiferromagnetic interactions in a hexanuclear mixed-valence CoIII2MnII2MnIV2 cluster sustained by a multidentate Schiff …

2019

The successful utilization of the “direct synthesis” approach yielded the unprecedented hexanuclear complex of formula [Co2MnII2MnIV2(L1)4Cl2(μ3-O)2(dmf)4]·2dmf (1) (H3L is the Schiff base derived from the condensation of salicylaldehyde and 3-aminopropane-1,2-diol). Single crystal X-ray analysis revealed that 1 crystallizes in the monoclinic system P21/c and it contains a rare mixed-valence {CoIII2MnII2MnIV2(μ2-O)8(μ3-O)2} core where all metal ions are linked through the phenolato and alkoxo groups of the L3− ligand. Besides the charge balance resulting from the X-ray structure, the oxidation state of the metal ions has been confirmed by XPS spectroscopy. Cryomagnetic studies indicate the …

DenticitySchiff baseValence (chemistry)Materials scienceSpin states010405 organic chemistryMetal ions in aqueous solution010402 general chemistry01 natural sciences0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryOxidation state[CHIM]Chemical SciencesAntiferromagnetism[CHIM.COOR]Chemical Sciences/Coordination chemistryComputingMilieux_MISCELLANEOUSMonoclinic crystal systemDalton Transactions
researchProduct

Designing dicyanamide bridged 1D molecular architecture from a mononuclear copper(II) Schiff base precursor: Syntheses, structural variations and mag…

2009

International audience; A new tridentate N2O donor Schiff base ligand [(C6H5C(OH)CHC(CH3)NCH2C5H4N)LH] was obtained by 1:1 condensation of benzoylacetone with 2-picolylamine and has been used to synthesise a mononuclear [CuLCl] (1) and an end-to-end dicyanamide bridged polynuclear {[Cu2(μ-L)2(μ2-1,5-(CN)2N)]ClO4}n (2) copper(II) complexes. The ligand, 1 and 2 were clearly characterised by elemental analysis, FT-IR, 1H NMR, UV–Vis spectral studies, electrochemical studies and in addition single crystal X-ray diffraction studies were performed for 1 and 2. The Schiff base ligand [LH] shows a significant variation in its coordination behaviour with copper(II) ion in absence and in presence of …

DenticityStereochemistrychemistry.chemical_element010402 general chemistry01 natural sciencesInorganic ChemistrySchiff basechemistry.chemical_compoundDeprotonationDicyanamide bridged polymerMagnetic properties[CHIM.CRIS]Chemical Sciences/CristallographyMaterials Chemistry[CHIM]Chemical SciencesPhysical and Theoretical ChemistryDicyanamideSchiff base010405 organic chemistryLigandMagnetic susceptibilityCopper0104 chemical sciencesCrystallography[CHIM.POLY]Chemical Sciences/PolymerschemistryMononuclear precursorProton NMRCopper(II) complexes2-Picolylamine and benzoylacetonePolyhedron
researchProduct