Search results for "Electrospray Ionization"

showing 10 items of 275 documents

Structural analysis of the lipid A isolated from Hafnia alvei 32 and PCM 1192 lipopolysaccharides[S]

2010

Hafnia alvei, a Gram-negative bacterium, is an opportunistic pathogen associated with mixed hospital infections, bacteremia, septicemia, and respiratory diseases. The majority of clinical symptoms of diseases caused by this bacterium have a lipopolysaccharide (LPS, endotoxin)-related origin. The lipid A structure affects the biological activity of endotoxins predominantly. Thus, the structure of H. alvei lipid A was analyzed for the first time. The major form, asymmetrically hexa-acylated lipid A built of beta-D-GlcpN4P-(1-->6)-alpha-D-GlcpN1P substituted with (R)-14:0(3-OH) at N-2 and O-3, 14:0(3-(R)-O-12:0) at N-2', and 14:0(3-(R)-O-14:0) at O-3', was identified by ESI-MS(n) and MALDI-tim…

Spectrometry Mass Electrospray IonizationendotoxinLipopolysaccharideAcylationOligosaccharidesQD415-436BiochemistryMicrobiologyLipid Achemistry.chemical_compoundOpportunistic pathogenEndocrinologyPalmitoylationEscherichiapalmitoylationmass spectrometryPolish Collection of MicroorganismsbiologyHafnia alveiBiological activityCell Biologybiology.organism_classificationOxygenHafnia alveiLipid AchemistrySpectrometry Mass Matrix-Assisted Laser Desorption-Ionizationlipids (amino acids peptides and proteins)BacteriaResearch ArticleJournal of Lipid Research
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Nitration of cathepsin D enhances its proteolytic activity during mammary gland remodelling after lactation

2009

Proteomic studies in the mammary gland of control lactating and weaned rats have shown that there is an increased pattern of nitrated proteins during weaning when compared with controls. Here we report the novel finding that cathepsin D is nitrated during weaning. The expression and protein levels of this enzyme are increased after 8 h of litter removal and this up-regulation declines 5 days after weaning. However, there is a marked delay in cathepsin D activity since it does not increase until 2 days post-weaning and remains high thereafter. In order to find out whether nitration of cathepsin D regulates its activity, iNOS (inducible nitric oxide synthase)−/− mice were used. The expression…

Spectrometry Mass Electrospray Ionizationmedicine.medical_specialtyImmunoblottingNitric Oxide Synthase Type IICathepsin DWeaningCathepsin DBiochemistryChromatography AffinityMice03 medical and health scienceschemistry.chemical_compoundMammary Glands Animal0302 clinical medicinePregnancyTandem Mass SpectrometryInternal medicineLactationmedicineAnimalsImmunoprecipitationLactationWeaningElectrophoresis Gel Two-DimensionalMolecular BiologyMammary gland involution030304 developmental biology0303 health sciencesNitratesbiologyReverse Transcriptase Polymerase Chain ReactionNitrotyrosineLife SciencesCell BiologyEnzyme assayRats3. Good healthNitric oxide synthaseEndocrinologymedicine.anatomical_structurechemistry030220 oncology & carcinogenesisbiology.proteinFemalePeroxynitriteChromatography LiquidBiochemical Journal
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Recognition of Li+ by a Salophen−UO2 Homodimeric Complex

2009

Self-assembly via mutual U-coordination of the salophen-UO(2) complex 1 creates a dimeric species which is shown to be useful for metal binding. Indeed, the 1 dimer has affinity for alkali metal cations and, interestingly, a marked selectivity for Li(+), determined by electrospray ionization mass spectrometry and (1)H NMR techniques. X-ray diffraction helped in the elucidation of the dimeric complex structure, which presents a crown-ether-type coordination site, in analogy to the more familiar 12-crown-4, responsible for the metal interaction. Comparison with isomer 2, and the salen derivative 3, increases the understanding of the behavior of such systems in solution and in the solid state.

StereochemistryDimerElectrospray ionizationSolid-stateAlkali metalInorganic ChemistryMetalchemistry.chemical_compoundCrystallographychemistryvisual_artProton NMRvisual_art.visual_art_mediumPhysical and Theoretical ChemistrySelectivityDerivative (chemistry)Inorganic Chemistry
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Triple bridged μ-phenoxo-bis(μ-carboxylate) and double bridged μ-phenoxo-μ1,1-azide/μ-methoxide dicopper(II) complexes: Syntheses, structures, magnet…

2013

Abstract The work in this paper presents syntheses, characterization, crystal structures, catecholase activity, electrospray ionization mass spectroscopy (ESI-MS positive), and magnetic properties of seven triple bridged μ-phenoxo-bis(μ-carboxylate) dicopper(II) complexes [CuII2L(μ-HCOO)2](ClO4)·CH3OH (1), [CuII2L(μ-CH3COO)2](ClO4) (2), [CuII2L(μ-CCl3COO)2(H2O)](ClO4) (3), [CuII2L(μ-CH3CH2COO)2](ClO4) (4), [CuII2L(μ-CH3CH2CH2COO)2](ClO4) (5), [CuII2L(μ-PhCOO)2](ClO4)·CH3CN (6) and [CuII2L(μ-o-ClPhCOO)2](ClO4) (7), one double bridged μ-phenoxo-μ1,1-azide system [CuII2L(μ1,1-N3)(N3)2] (8) and one double bridged μ-phenoxo-μ-methoxide system [CuII2L(μ-OCH3)(NCO)2] (9), derived from a new dinucl…

StereochemistryElectrospray ionizationCrystal structureMethoxideInorganic ChemistryMetalchemistry.chemical_compoundCrystallographychemistryMagnetochemistryvisual_artMaterials Chemistryvisual_art.visual_art_mediumAzideCarboxylatePhysical and Theoretical ChemistrySpectroscopyPolyhedron
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Diphenyltin(IV) complexes of the 5-[(E)-2-(aryl)-1-diazenyl]quinolin-8-olates: Synthesis and multinuclear NMR, 119Sn Mössbauer, electrospray ionizati…

2006

Abstract A series of cis-bis{5-[(E)-2-(aryl)-1-diazenyl]quinolinolato}diphenyltin(IV) complexes have been synthesized and characterized by 1H, 13C, 119Sn NMR, ESI-MS, IR and 119mSn Mossbauer spectroscopic techniques in combination with elemental analysis. The structures of a ligand L6H (i.e., 5-[(E)-2-(4-ethoxyphenyl)-1-diazenyl]quinolin-8-ol) and three diphenyltin(IV) complexes, viz., Ph2Sn(L1)2 · (CH3)2CO (1), Ph2Sn(L4)2 (4) and Ph2Sn(L5)2 (5) (L = 5-[(E)-2-(aryl)-1-diazenyl]quinolin-8-ol: aryl = phenyl – (L1H); 4′-methylphenyl – (L4H) and 4′-bromophenyl – (L5H)) were determined by single crystal X-ray diffraction. In general, the complexes were found to adopt a distorted cis-octahedral a…

StereochemistryLigandArylElectrospray ionizationOrganic Chemistrychemistry.chemical_elementCrystal structureBiochemistryMedicinal chemistryInorganic ChemistrySolventchemistry.chemical_compoundchemistryMössbauer spectroscopyMaterials ChemistryPhysical and Theoretical ChemistryTinSingle crystalJournal of Organometallic Chemistry
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Benzyl ions from 1,1-(2,2′-dimethoxyphenyl)-substituted 2-methylpropanes under electron ionization

2006

The electron ionization (EI)-induced fragmentations of a series of 1,1-(2,2'-dimethoxyphenyl)-substituted 2-methylpropanes (1-20) in both 70 eV and mass-analyzed ion kinetic energy (MIKE) spectra have been investigated. The EI-MS spectra of these compounds are characterized by the presence of abundant benzyl ions. These ions result from competitive hydrogen migration from the 2- and 2'-methoxy groups on the carbenium center of the diphenylmethyl cations formed by benzylic cleavage of the molecular ions. The relative abundances of the benzyl ions arising from such competitive processes are discussed and rationalized. The steric effect of the 3- or 3'-substituents is the main discriminating f…

Steric effectsSpectrometry Mass Electrospray IonizationHydrogenStereochemistrychemistry.chemical_elementKinetic energyMedicinal chemistrySpectral lineAnalytical ChemistryIonPropaneBenzyl CompoundsSpectroscopyElectron ionizationCARBON DOUBLE REARRANGEMENTMASS-SPECTRAHydrocarbons HalogenatedOrganic ChemistryCleavage (crystal)HYDROGEN-CARBONDIMETHOXY AROMATIC-COMPOUNDSSPECTROMETRYchemistryALKYLBENZENESSUBSTITUTED DIPHENYLMETHYL CATIONSHydrogenRapid Communications in Mass Spectrometry
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Mononuclear rearrangement of heterocycles in zwitterionic micelles of amine oxide surfactants.

2012

Abstract Rate constants for the mononuclear rearrangement (MRH) of Z -phenylhydrazones of some 5-substituted-3-benzoyl-1,2,4-oxadiazoles in water have been measured in the presence of zwitterionic micelles. The use of micellized N -tetradecyl- N , N -dimethylamineoxide (C 14 DMAO) as the reaction medium allowed to solubilize the otherwise water-insoluble oxadiazoles. Micellar rate effects were analyzed by using a simple pseudo-phase model and compared with those obtained in non-ionic micelles (Triton X-100). Evidence that both the rate of the rearrangement reaction and the binding of the substrates to the micelles are mainly governed by substrate hydrophobicity is obtained. The disagreement…

Steric effectsSpectrometry Mass Electrospray IonizationN-tetradecyl-NOctoxynolPhotochemistryMicelleMononuclear rearrangements of heterocycles (MHRs)Biomaterialschemistry.chemical_compoundSurface-Active AgentsColloid and Surface ChemistryReaction rate constantMicellar catalysiN-tetradecyl-NN-dimethylamineoxidePolymer chemistryRearrangement reactionzwitterionic micelleMicellesOxadiazolesHydrazonesSubstrate (chemistry)WaterSettore CHIM/06 - Chimica OrganicaSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsAmine oxideKineticschemistrySolubilitySolubilizationN-dimethylamineoxideThermodynamicsHydrophobic and Hydrophilic InteractionsMyristic AcidsDimethylaminesJournal of colloid and interface science
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Non-Centrosymmetric Tetrameric Assemblies of Tetramethylammonium Halides with Uranyl Salophen Complexes in the Solid State

2010

Ditopic salophen-UO(2) receptors 1-4 and 7 co-crystallize with tetramethylammonium (TMA) chloride and fluoride salts producing good quality crystals amenable for X-ray diffraction characterization. The arrangement of the receptor and salt units in the crystal lattice is such that tetrameric ball-shaped assemblies are formed, where an inner cluster of four TMA cations are surrounded by an outer shell of four UO(2)-bound anions. These elaborate architectures, which occur in all cases, regardless of a certain degree of structural modification on the receptors, lead to lattices that belong to non-centrosymmetric (NCS) space groups. Interestingly, the tetragonal symmetry of the tetrameric ball-s…

Tetramethylammonium010405 organic chemistryElectrospray ionizationInorganic chemistrySpace groupHalideCrystal structure010402 general chemistryMass spectrometry01 natural sciencesChloride0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundTetragonal crystal systemCrystallographychemistrymedicinePhysical and Theoretical Chemistrymedicine.drugInorganic Chemistry
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Determination of Fungi and Multi-Class Mycotoxins in Camelia sinensis and Herbal Teas and Dietary Exposure Assessment

2020

In this paper, a study of fungal and multi-mycotoxin contamination in 140 Camellia sinensis and 26 herbal teas marketed in Latvia is discussed. The analysis was performed using two-dimensional liquid chromatography with time-of-flight mass spectrometry (2D-LC-TOF-MS) and MALDI-TOF-MS. In total, 87% of the tea samples tested positive for 32 fungal species belonging to 17 genera, with the total enumeration of moulds ranging between 1.00 &times

Tolerable daily intakeOchratoxin ASpectrometry Mass Electrospray IonizationAflatoxinherbal teasHealth Toxicology and MutagenesisColony Count Microbiallcsh:MedicineToxicologyRisk Assessment01 natural sciencesArticleCamellia sinensisDietary Exposurechemistry.chemical_compound0404 agricultural biotechnologymycotoxinsHumansCamellia sinensis2D-LC-TOF-MSFood scienceMycotoxin<i>Camellia sinensis</i> teasTeabiologyDietary exposureCamellia sinensis teaslcsh:R010401 analytical chemistrydietary exposure assessmentfood and beverages04 agricultural and veterinary sciencesContaminationAlternariabiology.organism_classificationLatviaMALDI-TOF-MS040401 food science0104 chemical scienceschemistryConsumer Product SafetySpectrometry Mass Matrix-Assisted Laser Desorption-Ionizationfungi<i>Camellia sinensis </i>teasTeas HerbalChromatography LiquidToxins
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Synthesis and copper-mediated nuclease activity of a tetracationic tris(2,2′-bipyridine) ligand

2009

Abstract We report herein the synthesis of a novel tetracationic tris(2,2′-bipyridine) ligand 4 . We show that this ligand metalated with copper(II), and in the presence of ascorbate as a reducing agent, strongly damages pUC18 plasmid DNA. Copper complex formation was demonstrated by ESI-MS (electrospray ionization-mass spectrum) at a 1:3 ligand to metal ratio. Binding of both 4 and its copper(II) complex to CT-DNA (calf thymus DNA) was characterized by viscosimetry, thermal denaturation and fluorescence-based competition assays. The viscosimetric data indicated that 4 and its copper(II) complex bind DNA through partial intercalation and thermal denaturation studies revealed a significant i…

TrisSpectrometry Mass Electrospray IonizationDeoxyribonucleasesChemistryIntercalation (chemistry)chemistry.chemical_elementDNALigandsPhotochemistryLigand (biochemistry)BiochemistryCopper22'-BipyridineInorganic Chemistrychemistry.chemical_compound22'-DipyridylPolymer chemistryAnimalsHydroxyl radicalDNA CleavageEthidium bromideCopperDNAJournal of Inorganic Biochemistry
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