Search results for "Spectroscopy"

showing 10 items of 10293 documents

Field desorption mass spectrometric characterization of thiol conjugates related to the oxidative metabolism of the anticancer drug 4′-(9-acridinylam…

1983

Conjugation products with glutathione (GSH) and other endogenous thiol derivatives related to the oxidative metabolism of the anticancer drug, 4′-(9-acridinlyamino) methanesulfon-m-anisidide (m-AMSA) were synthesized and characterized by field desorption mass spectrometry. The primary microsomal oxidation product of m-AMSA, m-AQDI, was prepared by MnO2 oxidation of the parent drug and reacted with equimolar GSH, cysteine, N-acetylcysteine and N-acetylcysteine methyl ester to form m-AMSA-(5′)-thiol conjugates linkedat the aniline ring, as major products. Field desorption mass spectra of the conjugates provided abundant [MH]plus; ions, and characteristic fragment ions by cleavage at the thioe…

AmsacrineAminoacridinesStereochemistryGlutathioneMedicinal chemistryMass SpectrometryRatsAdductchemistry.chemical_compoundAnilineLiverchemistryThioetherThiolysisAcridineAnimalsMoietyCysteamineSulfhydryl CompoundsBiotransformationSpectroscopyCysteineBiological Mass Spectrometry
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Identification of conjugation and cleavage products in the thiolytic metabolism of the anticancer drug 4'-(9-acridinylamino)methanesulfon-m-anisidide.

1981

Conjugation and cleavage products in the thiolytic metabolism of the anticancer drug 4′ -(9-acridinyl amino)methanesulfon-m-anisidide were identified primarily by high-pressure liquid chromatography in combination with field desorption mass spectrometry. The spontaneous metabolic pathway of the drug, as related to its susceptibility to nucleophilic attack by endogenous thiols at the 9-carbon atom of the acridine moiety, has been studied. Among the metabolite fraction of 4′-(9-acridinylamino)methanesulfon-m-anisidide excreted in rat bile after administration of a therapeutic dose, a conjugate was identified as the 9-acridinyl thioether of glutathione. This conjugation product and the corresp…

AmsacrineMaleStereochemistryMetaboliteAntineoplastic AgentsBiochemistryMass Spectrometrychemistry.chemical_compoundThioetherAnimalsBileSpectroscopyChromatography High Pressure LiquidAminoacridinesRats Inbred StrainsGlutathioneMetabolismGlutathioneRatsMetabolic pathwaychemistryAcridineMolecular MedicineChromatography Thin LayerCysteineConjugateBiomedical mass spectrometry
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Stirring effects in amyloid fibril formation

2014

Amyloid Shear force Spectroscopy
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Decoding vibrational states of Concanavalin A amyloid fibrils.

2015

International audience; Amyloid and amyloid-like fibrils are a general class of protein aggregates and represent a central topic in life sciences for their involvement in several neurodegenerative disorders and their unique mechanical and supramolecular morphological properties. Both their biological role and their physical properties, including their high mechanical stability and thermodynamic inertia, are related to the structural arrangement of proteins in the aggregates at molecular level. Significant variations may exist in the supramolecular organization of the commonly termed cross-β structure that constitutes the amyloid core. In this context, a fine knowledge of the structural deta…

AmyloidAbsorption spectroscopy[SDV]Life Sciences [q-bio]BiophysicsSupramolecular chemistry02 engineering and technologymacromolecular substancesProtein aggregationAntiparallel (biochemistry)FibrilSpectrum Analysis RamanBiochemistryVibrationProtein Structure Secondary03 medical and health sciencessymbols.namesakeSpectroscopy Fourier Transform InfraredConcanavalin AHumansFourier transform infrared spectroscopyRaman030304 developmental biology0303 health sciencesChemistryOrganic ChemistryIntermolecular force021001 nanoscience & nanotechnologyAmyloid FTIR RAMAN hydration water THz spectroscopy[SDV] Life Sciences [q-bio]CrystallographyFTIRTerahertz spectroscopysymbolsBiophysicsFibrils0210 nano-technologyRaman spectroscopy
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Concanavalin A aggregation and toxicity on cell cultures

2009

A number of neurodegenerative diseases are known to involve protein aggregation. Common mechanisms and structural properties of amyloids are thought to be involved in aggregation-related cytotoxicity. In this context we propose an experimental study on Concanavalin A (Con A) aggregation and use it as a model to study the relationship between cell toxicity and aggregation processes. Depending on solution conditions, Con A aggregation has been monitored by static and dynamic light scattering, Thioflavin T emission, and FTIR absorption. The morphology of different aggregate species was verified by means of Atomic Force Microscopy and Confocal Microscopy. During the aggregation pathway the nati…

AmyloidCell SurvivalBiophysicsApoptosisContext (language use)Protein aggregationMicroscopy Atomic ForceFibrilBiochemistryAnalytical Chemistrychemistry.chemical_compoundProtein structureCell Line TumorSpectroscopy Fourier Transform InfraredConcanavalin AExtracellularHumansProtein Structure QuaternaryCytotoxicityMolecular BiologyNeuronsbiologyChemistryBiochemistryConcanavalin Abiology.proteinThioflavinProtein aggregation Amyloids Citotoxicity Oligomers
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Thioflavin T Hydroxylation at Basic pH and Its Effect on Amyloid Fibril Detection

2008

The fluorescent dye thioflavin T (ThT) is commonly used for in situ amyloid fibril detection. In this work, we focused on the spectroscopic properties and chemical stability of ThT in aqueous solution as a function of pH, temperature, and dye concentration. A reversible hydroxylation process occurs in alkaline solutions, which was characterized using a combination of UV-vis absorption spectroscopy, proton NMR, and density functional theory (DFT). On the basis of these studies, we propose a chemical structure for the hydroxylated form. Finally, by means of fluorescence spectroscopy, ThT hydroxylation effects on in situ amyloid detection have been investigated, providing new insights on the e…

AmyloidMagnetic Resonance SpectroscopyAqueous solutionTemperatureThioflavin T AmyloidHydrogen-Ion ConcentrationHydroxylationPhotochemistryFibrilFluorescenceFluorescence spectroscopySurfaces Coatings and FilmsHydroxylationKineticsThiazoleschemistry.chemical_compoundchemistryMaterials ChemistryProton NMROrganic chemistrySpectrophotometry UltravioletThioflavinChemical stabilityBenzothiazolesPhysical and Theoretical ChemistryThe Journal of Physical Chemistry B
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The Boson Peak of Amyloid Fibrils: Probing the Softness of Protein Aggregates by Inelastic Neutron Scattering

2014

Proteins and polypeptides are characterized by low-frequency vibrations in the terahertz regime responsible for the so-called "boson peak". The shape and position of this peak are related to the mechanical properties of peptide chains. Amyloid fibrils are ordered macromolecular assemblies, spontaneously formed in nature, characterized by unique biological and nanomechanical properties. In this work, we investigate the effects of the amyloid state and its polymorphism on the boson peak. We used inelastic neutron scattering to probe low-frequency vibrations of the glucagon polypeptide in the native state and in two different amyloid morphologies in both dry and hydrated sample states. The dat…

AmyloidPhysics::Biological PhysicsQuantitative Biology::BiomoleculesChemistryProtein dynamicsNeutron diffractionNeutron scatteringProtein aggregationFibrilVibrationAmyloid Protein dynamics collective motions boson peakInelastic neutron scatteringSurfaces Coatings and FilmsNeutron DiffractionMicroscopy Electron TransmissionChemical physicsMolecular vibrationSpectroscopy Fourier Transform InfraredMaterials ChemistryNative statePhysical and Theoretical ChemistryAtomic physics
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H2-Antihistaminika, 36. Mitt. Isolamtidin und Analoge

1987

Isolamtidin (9a), ein Stellungsisomer des Lamtidins (8a), sowie die analogen N3-substituierten 1-Methyl-1H-1,2,4-triazol-3,5-diamine 9e-i, k wurden durch spezifische Synthese dargestellt und am isolierten Meerschweinchenvorhof und an der histaminstimulierten Sauresekretion der narkotisierten Ratte auf H2-antagonistische Wirkung untersucht. H2-Antihistaminics, XXXVI: Isolamitidine and Analogues Isolamitidine (9a), a position isomer of lamtidine (8a), as well as the analogous N3-substituted 1-methyl-1H-1,2,4-triazole-3,5-diamines 9e-i, k were prepared and tested for H2-antagonistic activity on the isolated guinea-pig atrium and towards the histamine-stimulated acid secretion of the anaestheti…

Anaesthetized ratIsolamtidinAtrium (architecture)ChemistryStereochemistryDrug DiscoveryPharmaceutical ScienceBiological activityNuclear magnetic resonance spectroscopyArchiv der Pharmazie
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The generalized H-point standard-additions method to determine analytes present in two different chemical forms in unknown matrix samples. Part II. C…

2000

The generalized H-point standard-additions method (GHPSAM) is used in order to obtain the total Cr(VI) and chromate concentration in water samples whose matrices are completely unknown. Moreover, a new methodology, which is a modification of the GHPSAM, is proposed for the simultaneous determination of the two major chemical forms of Cr(VI) present in the sample. The method is based on the location of spectral intervals where the behaviour of the interferent absorbance can be considered as linear. From these intervals, the analyte concentration free from bias error can be estimated. Spiked samples of dig and harbour water measured in the UV–visible spectral region have been tested to check …

AnalyteAbsorption spectroscopyChromate conversion coatingChemistryAnalytical chemistryBiochemistryAnalytical ChemistryChemometricsAbsorbanceMatrix (mathematics)Standard additionElectrochemistryEnvironmental ChemistryQuantitative analysis (chemistry)SpectroscopyThe Analyst
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Apparent content curves: description and analytical applications. Resolution of binary mixtures

1992

The apparent content curves and their analytical applications are described. Basing on these curves a mathematical method, which permits the identification of the interfering component present in a binary mixture as well as the determination of the contents of both constituents, is proposed. The existence of considerable interaction coefficients is not an impediment for its application. Besides, the analyte contents in the mixture can be obtained without the use of standard interference solutions. The proposed procedure is applied to the analysis of mixtures of dyes with overlapping absorption spectra.

AnalyteAbsorption spectroscopyResolution (mass spectrometry)ChemistryComponent (thermodynamics)Content (measure theory)Analytical chemistryBinary numberInterference (wave propagation)Biological systemBiochemistryAnalytical ChemistryFresenius' Journal of Analytical Chemistry
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