Search results for "molecular mass"

showing 10 items of 155 documents

Proteomics of tear fluid in thyroid-associated orbitopathy.

2012

Proteomics and mass spectrometry are useful tools for peptide screening in body fluids. In thyroid-associated orbitopathy (TAO), evidence for lacrimal gland involvement with altered composition of tears has been reported. Our objective was to detect and evaluate potential changes in the proteomic patterns of tear fluid in TAO.Tear fluid was collected from 45 patients with TAO and 15 healthy controls. Tear proteins were analyzed using surface-enhanced laser desorption/ionization time-of-flight mass spectrometry, and peptides were identified using matrix-assisted laser desorption/ionization time-of-flight technology.Peptides with molecular weights 3808 Dalton (Da, p=0.004), 3734 Da (p=0.034),…

AdultMaleProteomicsmedicine.medical_specialtyEndocrinology Diabetes and MetabolismDown-RegulationPeptideLacrimal glandProteomicsMass spectrometryEndocrinologyInternal medicinemedicineHumansEye ProteinsAgedchemistry.chemical_classificationMolecular massThyroidLacrimal ApparatusMiddle AgedUp-RegulationGraves OphthalmopathyMatrix-assisted laser desorption/ionizationmedicine.anatomical_structureEndocrinologychemistrySpectrometry Mass Matrix-Assisted Laser Desorption-IonizationTearsTearsSalivary CystatinsFemaleMuramidasePeptidesbeta 2-MicroglobulinThyroid : official journal of the American Thyroid Association
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Homodimeric murine interleukin-3 agonists indicate that ligand dimerization is important for high-affinity receptor complex formation.

1994

Homodimeric murine interleukin 3 (mIL-3) agonists were generated by intermolecular cystine-bonding. Steady-state binding assays and association kinetics performed at 4 degrees C using these agonists revealed specific binding to both the high- and low-affinity receptor. DSS-mediated crosslinking studies performed at 4 degrees C with agonist concentrations compatible with high-affinity receptor complex formation allowed to detect protein complexes of the alpha chain, the beta chain(s) and the high-affinity receptor complex migrating with apparent molecular weights of 90 kDa, 140 kDa, and above 180 kDa, respectively. In contrast, monomeric mIL-3 was crosslinked to the alpha chain receptor only…

AgonistReceptor complexmedicine.drug_classMacromolecular SubstancesClinical BiochemistryInterleukin-17 receptorLigandsProtein Structure SecondaryCell LineMiceEndocrinologymedicineAnimalsReceptorProtease-activated receptor 2Interleukin 3Cell Line TransformedMolecular massChemistryGranulocyte-Macrophage Colony-Stimulating FactorCell BiologyLigand (biochemistry)Receptors Interleukin-3Recombinant ProteinsKineticsBiochemistryCystineBiological AssayElectrophoresis Polyacrylamide GelInterleukin-3Interleukin-5Cell DivisionThymidineGrowth factors (Chur, Switzerland)
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Characterization and determination of poly(vinylpyrrolidone) by complexation with an anionic azo-dye and nonequilibrium capillary electrophoresis

2009

Using capillary zone electrophoresis in nonequilibrium conditions, the complexes of poly(vinylpyrrolidone) (PVP) with anionic azo-dyes dissociate following a first-order kinetics. Two peaks due to the remaining PVP-dye complexes and the equilibrium concentration of the free dye, plus an exponential region due to the dye liberated by the complexes during the electrophoretic run, are obtained. This behaviour was closely similar to that described in the literature for protein-probe and DNA-protein mixtures, upon application of the technique known as nonequilibrium capillary electrophoresis of equilibrium mixtures or NECEEM. Using Congo Red and Acid Blue 113, information about the maximal stoic…

AnionsDetergentsKineticsmacromolecular substancesBiochemistryAnalytical Chemistrychemistry.chemical_compoundCapillary electrophoresisColoring Agentschemistry.chemical_classificationChromatographyMolecular massPolymer characterizationOrganic Chemistrytechnology industry and agricultureElectrophoresis CapillaryPovidoneGeneral MedicinePolymerCongo redMolecular WeightKineticsElectrophoresischemistryCalibrationAzo CompoundsStoichiometryJournal of Chromatography A
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Comparison of outer membrane protein profiles of Vibrio vulnificus biotypes 1 and 2.

1993

The outer membrane proteins of 17 Vibrio vulnificus biotype 2 strains from Japanese and European eels, and 12 biotype 1 strains from clinical and environmental sources have been compared. The overall profile in both biotypes was similar, and a major protein band of molecular mass 36 kDa was detected in the majority of the strains. Differences in the minor bands allowed differentiation of strains from different origins, suggesting that outer membrane protein profiles could be useful as epidemiological markers in the species V. vulnificus. Immunoblotting with antisera to whole cells of selected strains of biotypes 1 and 2 showed a strong antigenic response to outer membrane proteins 66, 60, 4…

AntigenicityAntigens BacterialEelsStrain (chemistry)biologyMolecular massBlotting WesternVibrio vulnificusbiology.organism_classificationMicrobiologyMicrobiologyBacterial Typing TechniquesMolecular WeightMembrane proteinSpecies SpecificityVibrionaceaeGeneticsAnimalsElectrophoresis Polyacrylamide GelBacterial outer membraneMolecular BiologyBacteriaBacterial Outer Membrane ProteinsVibrioFEMS microbiology letters
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Incorporation of specific wall proteins during yeast and mycelial protoplast regeneration in Candida albicans

1994

The kinectics of incorporation of two precursor mannoproteins into the regenerating cell wall of Candida albicans protoplasts have been followed at 28°C and 37°C using two monoclonal antibodies specific for protein epitopes (MAb 1B12 and 4C12) as probes. Both molecules were secreted from the beginning of the regeneration process, and their incorporation was retarded significantly. Analysis of the secreted materials by Western immunoblotting with MAb 1B12 allowed the identification of two closely migrating bands at apparent Mr higher than 170 kDa and significant amounts of a highly polydisperse material of even greater molecular mass. Some of these mannoproteinaceous species carried both N- …

Antigens FungalFluorescent Antibody TechniqueMannoseBiochemistryMicrobiologyFungal ProteinsCell wallEpitopeschemistry.chemical_compoundCell WallCandida albicansGeneticsCandida albicansMolecular Biologychemistry.chemical_classificationMembrane GlycoproteinsMolecular massbiologyProtoplastsTemperatureAntibodies MonoclonalGeneral MedicineTunicamycinProtoplastbiology.organism_classificationMolecular WeightBiochemistrychemistryConcanavalin Abiology.proteinGlycoproteinArchives of Microbiology
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Gelchromatographie. 8. Mitt.: Vernetzte copolymere des vinylacetats

1969

Die Eigenschaften von vernetzten Copolymeren des Vinylacetats wurden in Abhangigkeit von den Herstellungsbedingungen gepruft. Als Vernetzungsmittel dienten Divinyladipat und Butandiol-(1.4)-divinylather. Mit homogen-vernetzten Gelen konnen Ausschlusmolekulargewichte bis etwa 4000 erzielt werden: zwischen dem spezifischen Gelbettvolumen und dem Ausschlusmolekulargewicht besteht eine lineare Beziehung. Die heterogen-vernetzende Copolymerisation des Vinylacetats in Gegenwart verschiedener inerter Verdunnungsmittel fuhrt zu Gelen mit Ausschlusmolekulargewichten uber 106. Die vernetzten Copolymeren wurden durch ihre scheinbare Dichte, durch die Aufnahme von Losungs- und Fallungsmitteln, durch di…

Apparent densitychemistry.chemical_compoundLinear relationshipMolecular massChemistryAdipatePolymer chemistryCopolymerVinyl acetatemedicineSwellingmedicine.symptomDie Makromolekulare Chemie
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Mark-Houwink Parameters of Biosynthetic Poly(γ-glutamic acid) in Aqueous Solution

2001

A combined viscosity–light scattering–gel permeation chromatography (GPC) study was carried out on bacterially produced poly(γ-glutamic acid) (PGGA). PGGA samples with weight-average molecular weights ranging from 8×104 up to 8×105 g·mol–1 dissolved in phosphate buffer at 0.13 M ionic strength were used. It was found that the Mark–Houwink relation is acceptably obeyed, giving K and a values of 1.84×10–6 dL·g–1 and 1.16, respectively. As expected, GPC analysis showed that PGGA does not follow the universal calibration plot and that deviations can not be avoided by modifying the ionic strength.

Aqueous solutionChromatographyPolymers and PlasticsMolecular massChemistryCalibration curveOrganic ChemistryMark–Houwink equationGlutamic acidPermeationCondensed Matter PhysicsIonic strengthMaterials ChemistryA valuePhysical and Theoretical ChemistryMacromolecular Chemistry and Physics
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Synthesis and characterisation of N-glycosyl amines from the reaction between 4,6-O-benzylidene-D-glucopyranose and substituted aromatic amines and a…

2001

Twelve N-glycosyl amines were synthesised using 4,6-O–benzylidene-D-glucopyranose and different substituted aromatic amines, including some diamines that resulted in bis-glycosyl amines. Another set of six N–glycosyl amines was synthesised using different hexoses and pentoses and 2–(o–aminophenyl)benzimidazole. All compounds were isolated as solid products and purified, their elemental compositions were established, and these were characterised by NMR (1H and 13C), UV–Vis, and FTIR spectroscopy, by FAB mass spectrometry (molecular-ion peaks gave molecular weights), and by their optical rotations. While the protected saccharide, 4,6-O-benzylidene-D-glucopyranose, exists as a mixture of β and…

BenzimidazoleAnomerGlycosylationOptical RotationNuclear Magnetic Resonance SpectroscopyMolecular Sequence DataPentosesSynthesis (Chemical)macromolecular substancesMass spectrometryBiochemistryMedicinal chemistryMass SpectrometryAnalytical Chemistrychemistry.chemical_compoundOrganic chemistryGlycosylFourier transform infrared spectroscopyAminesPolycyclic Aromatic HydrocarbonsNuclear Magnetic Resonance BiomolecularHexosesMolecular massChemistryChemical shiftOrganic ChemistryHydrogen BondingGeneral MedicineD-GlucopyranoseMolecular WeightGlucoseCarbohydrate Sequencelipids (amino acids peptides and proteins)BenzimidazolesCarbohydrate research
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Synthesis of a New Disulfide Affinity Adsorbent for Purification of Human Uterine Progesterone Receptor

2005

For purification of the human uterine progesterone receptor, an affinity adsorbent was synthesized in which the specific ligand (16 alpha-ethyl-3-oxo-19nor-androst-4-ene 17 beta-carboxylic acid) was bound to derivatized celulose using a disulfide-group-containing spacer. The purified receptor protein, isolated by reductive cleavage of the disulfide bond, bound the synthetic gestagen R5020 with high affinity (Kd 12.2 nmol/l). The affinity gel was highly efficient. A 24000-fold purification of progesterone receptor with a recovery of 40% could be achieved in a single step within 6 h. By means of dodecyl sulphate/polyacrylamide gel electrophoresis two main polypeptides with molecular weights o…

Binding CompetitiveBiochemistryChromatography Affinitychemistry.chemical_compoundCytosolAdsorptionPregnenedionesProgesterone receptorCentrifugation Density GradientHumansCelluloseReceptorPolyacrylamide gel electrophoresisChromatographyProgesterone CongenersMolecular massUterusDisulfide bondLigand (biochemistry)Resins SyntheticchemistryBiochemistryElectrophoresis Polyacrylamide GelFemaleAdsorptionReceptors ProgesteroneEuropean Journal of Biochemistry
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Biocompatibility of alginates for grafting: impact of alginate molecular weight.

2003

Optimising microencapsulation technology towards the effective clinical transplantation has created the need for highly biocompatible alginates. Therefore, in this study the biocompatibility of different beads prepared from alginates with varying average molecular weight was examined. In some experiments the beads were covered with a multilayer membrane surrounded by an alginate layer. First of all, we found that beads made of a lower weight average alginate elicted a much stronger fibrotic response compared to beads made of a higher weight average alginate (LV-alginate > MV-alginate). The results were confirmed by the observation that the extent of tissue fibrosis was significantly increas…

BiocompatibilityMolecular massChemistryAlginatesDrug CompoundingBiomedical EngineeringBiocompatible MaterialsGraftingBiocompatible materialFibrosisMicrospheresRatsTransplantationMolecular WeightRats Sprague-DawleyViscosityChemical engineeringImplants ExperimentalTissue fibrosisMaterials TestingMolar mass distributionAnimalsBiotechnologyBiomedical engineeringArtificial cells, blood substitutes, and immobilization biotechnology
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