Search results for "Cross-link"

showing 10 items of 99 documents

Surface molecularly imprinted silica for selective solid-phase extraction of biochanin A, daidzein and genistein from urine samples

2015

Selective molecularly imprinted silica polymer (SiO2MIP) for extraction of biochanin A, daidzein and genistein was synthesized using the surface molecular imprinting technique with the silica gel as a support. Biochanin A (BCA) was used as a template, 3-aminopropyltriethoxysilane (APTES) as a functional monomer, and tetraethoxysilicane (TEOS) as a cross-linker. Non-imprinted polymer with the sol–gel process (SiO2NIP) was also prepared for comparison. The synthesized polymers were characterized by Fourier transform infrared spectrometry (FTIR), scanning electron microscopy (SEM) and a standard Brunauer-Emett-Teller (BET) and Barret–Joyner–Halenda (BJH) analysis. The obtained results indicate…

PolymersSilica Gelmolecularly imprinted polymerBiochemistryAnalytical ChemistryBiochanin AMolecular Imprintingchemistry.chemical_compoundHumanssolid-phase extractionSolid phase extractionFourier transform infrared spectroscopyChromatographyPropylaminesChemistrySilica gelSolid Phase ExtractionOrganic ChemistryExtraction (chemistry)DaidzeinMolecularly imprinted polymerWaterGeneral MedicineSilanesSilicon DioxideGenisteinIsoflavonesurineCross-Linking ReagentsNanoparticlesFemaleMolecular imprintingPorosityJournal of Chromatography A
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Identification of ERp29, an endoplasmic reticulum lumenal protein, as a new member of the thyroglobulin folding complex.

2002

Folding and post-translational modification of the thyroid hormone precursor, thyroglobulin (Tg), in the endoplasmic reticulum (ER) of the thyroid epithelial cells is facilitated by several molecular chaperones and folding enzymes, such as BiP, GRP94, calnexin, protein disulfide isomerase, ERp72, and others. They have been shown to associate simultaneously and/or sequentially with Tg in the course of its maturation, thus forming large heterocomplexes in the ER of thyrocytes. Here we present evidence that such complexes include a novel member, an ER-resident lumenal protein, ERp29, which is present in all mammalian tissues with exceptionally high levels of expression in the secretory cells. …

Protein DenaturationProtein FoldingImmunoprecipitationmedicine.medical_treatmentBlotting WesternThyroid GlandThyrotropinBiologyEndoplasmic ReticulumLigandsBiochemistryThyroglobulinRats Sprague-DawleyCalnexinmedicineCentrifugation Density GradientAnimalsUreaSecretionProtein disulfide-isomeraseMolecular BiologyCells CulturedHeat-Shock ProteinsThyroid Epithelial CellsChromatographyEndoplasmic reticulumCell BiologyPrecipitin TestsRatsCross-Linking ReagentsBiochemistryLiverMicroscopy FluorescenceMicrosomes LiverProtein foldingThyroglobulinProtein BindingThe Journal of biological chemistry
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Self-assembly of biopolymeric structures below the threshold of random cross-link percolation

1996

Self-assembly of extended structures via cross-linking of individual biomolecules often occurs in solutions at concentrations well below the estimated threshold for random cross-link percolation. This requires solute-solute correlations. Here we study bovine serum albumin. Its unfolding causes the appearance of an instability region of the sol, not observed for native bovine serum albumin. As a consequence, spinodal demixing of the sol is observed. The thermodynamic phase transition corresponding to this demixing is the determinative symmetry-breaking step allowing the subsequent occurrence of (correlated) cross-linking and its progress up to the topological phase transition of gelation. Th…

Protein FoldingSpinodalPhase transitionProtein ConformationBiophysicsIn Vitro TechniquesInstabilityBiophysical PhenomenaBiopolymersDrug StabilityAnimalsTopological orderBovine serum albuminQuantitative Biology::BiomoleculesMolecular StructurebiologyChemistrySerum Albumin BovineCrystallographyCross-Linking ReagentsChemical physicsPercolationbiology.proteinThermodynamicsCattleProtein foldingSelf-assemblyGelsResearch Article
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Intermolecular Cystine-Bonding of Murine Interleukin 2 Indicates that Ligand Dimerization is Important for the Formation of the High-Affinity Recepto…

1992

Interleukin 2 is thought to be active as a monomeric protein. As the nonessential Cys-140 of murine interleukin 2 (mIL2) is located in the hydrophobic interface of the amphiphilic F domain it was successfully used to stabilize hydrophobic amino acid contacts between two mIL2 cores yielding biologically active cystine-bonded dimeric mIL2. (3H) thymidine incorporation assays with intermolecular cystine-bonded or monomeric mIL2 revealed almost identical median effective concentrations (EC50) and high-affinity dissociation constants (Kdh), respectively. Comparative binding and internalization assays suggest that one cystine-bonded dimeric or two monomeric mIL2 molecules bind to the high-affinit…

Receptor complexStereochemistryMolecular Sequence DataClinical BiochemistrySuccinimidesLigandsCell LineMicechemistry.chemical_compoundEndocrinologyAnimalsAmino Acid SequenceReceptorPeptide sequencechemistry.chemical_classificationMolecular massLigandReceptors Interleukin-2Cell BiologyAmino acidDissociation constantKineticsCross-Linking ReagentsMonomerchemistryBiochemistryCystineInterleukin-2Cell DivisionGrowth Factors
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The N-terminal Amino Group of [Tyr8]Bradykinin Is Bound Adjacent to Analogous Amino Acids of the Human and Rat B2 Receptor

1996

To obtain data of the bradykinin B2 receptor's agonist binding site, we used a combined approach of affinity labeling and "immunoidentification" of receptor fragments generated by cyanogen bromide cleavage. Domain-specific antibodies to the various extracellular receptor domains were applied to detect receptor fragments with covalently attached [125I-Tyr8]bradykinin. As a cross-linker we used the homobifunctional reagent disuccinimidyl tartarate (DST), which reacts preferentially with primary amines. With this technique a [125I-Tyr8]bradykinin-labeled receptor fragment derived from the third extracellular domain was identified. The epsilon-amino group of lysine (Lys172) of the human B2 rece…

Receptor Bradykinin B2StereochemistryAffinity labelMolecular Sequence DataBradykininBradykininTransfectionBiochemistryProtein Structure SecondaryCell LineIodine Radioisotopeschemistry.chemical_compoundAnimalsHumansAmino Acid SequenceBradykinin receptorReceptorMolecular BiologyPeptide sequencechemistry.chemical_classificationBinding SitesAffinity labelingbiologyLysineReceptors BradykininAffinity LabelsCell BiologyRecombinant ProteinsRatsAmino acidCross-Linking ReagentschemistryBiochemistryCOS CellsFree fatty acid receptorbiology.proteinJournal of Biological Chemistry
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Infinite coordination polymer networks metallogelation of aminopyridine conjugates and in situ silver nanoparticle formation

2018

Herein we report silver(i) directed infinite coordination polymer network (ICPN) induced self-assembly of low molecular weight organic ligands leading to metallogelation. Structurally simple ligands are derived from 3-aminopyridine and 4-aminopyridine conjugates which are composed of either pyridine or 2,2'-bipyridine cores. The cation specific gelation was found to be independent of the counter anion, leading to highly entangled fibrillar networks facilitating the immobilization of solvent molecules. Rheological studies revealed that the elastic storage modulus (G') of a given gelator molecule is counter anion dependent. The metallogels derived from ligands containing a bipyridine core dis…

STABILIZATIONSilverCoordination polymerNanoparticleMetal Nanoparticles02 engineering and technologyorganometalliyhdisteet010402 general chemistry01 natural sciencesSilver nanoparticlePolymerizationchemistry.chemical_compoundBipyridinePyridineorganometallic compoundsMoleculePARTICLESCRYSTAL-STRUCTURES4-Aminopyridinepolymeeritta116GELSpolymersgeelitHYBRID MATERIALSta114General Chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsGELATION0104 chemical sciencesCrystallographyREDUCTIONCross-Linking ReagentschemistryPolymerizationMETALLUMINESCENCEPHASE-TRANSITIONCoordination polymerizationnanohiukkasetnanoparticles0210 nano-technologyRheologySOFT MATTER
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Non-cross-linked porcine-based collagen I-III membranes do not require high vascularization rates for their integration within the implantation bed: …

2012

There are conflicting reports concerning the tissue reaction of small animals to porcine-based, non-cross-linked collagen I-III membranes/matrices for use in guided tissue/bone regeneration. The fast degradation of these membranes/matrices combined with transmembrane vascularization within 4 weeks has been observed in rats compared with the slow vascularization and continuous integration observed in mice. The aim of the present study was to analyze the tissue reaction to a porcine-based non-cross-linked collagen I-III membrane in mice. Using a subcutaneous implantation model, the membrane was implanted subcutaneously in mice for up to 60 days. The extent of scaffold vascularization, tissue …

ScaffoldMaterials scienceBarrier membraneSus scrofaBiomedical EngineeringFibroinNeovascularization PhysiologicBiochemistryCollagen Type IBiomaterialsProsthesis ImplantationMicemedicineAnimalsBone regenerationMolecular BiologyPolytetrafluoroethyleneMembranesTissue ScaffoldsGranulation tissueMembranes ArtificialGeneral MedicineImmunohistochemistryTransmembrane proteinRatsmedicine.anatomical_structureMembraneCollagen Type IIICross-Linking ReagentsGiant cellBiophysicsMicroscopy Electron ScanningFemaleFibroinsBiotechnologyBiomedical engineeringActa biomaterialia
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Photocrosslinkable polyaspartamide/polylactide copolymer and its porous scaffolds for chondrocytes

2017

With the aim to produce, by a simple and reproducible technique, porous scaffolds potentially employable for tissue engineering purposes, in this work, we have synthesized a methacrylate (MA) copolymer of α,β-poly(N-2-hydroxyethyl)-dl-aspartamide (PHEA) and polylactic acid (PLA). PHEA-PLA-MA has been dissolved in organic solvent at different concentrations in the presence of NaCl particles with different granulometry, and through UV irradiation and further salt leaching technique, various porous scaffolds have been prepared. Obtained samples have been characterized by scanning electron microscopy and their porosity has been evaluated as well as their degradation profile in aqueous medium in…

ScaffoldMaterials scienceSwineScanning electron microscopePolyestersBioengineering02 engineering and technology010402 general chemistryMethacrylate01 natural sciencesCartilage regeneration; Photocrosslinking; Porous scaffolds; αβ-poly(N-2-hydroxyethyl)-DL-aspartamideBiomaterialschemistry.chemical_compoundChondrocytesPorous scaffoldTissue engineeringPolylactic acidPolymer chemistryCopolymerAnimalsPorosityPhotocrosslinkingαβ-poly(N-2-hydroxyethyl)-DL-aspartamideTissue EngineeringTissue Scaffoldstechnology industry and agriculturePhotochemical Processes021001 nanoscience & nanotechnology0104 chemical sciencesCross-Linking ReagentschemistryChemical engineeringCartilage regenerationSettore CHIM/09 - Farmaceutico Tecnologico ApplicativoMechanics of MaterialsCattleLeaching (metallurgy)0210 nano-technologyPorosityMaterials Science and Engineering: C
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Bioactive glass ions induce efficient osteogenic differentiation of human adipose stem cells encapsulated in gellan gum and collagen type I hydrogels

2019

Abstract Background Due to unmet need for bone augmentation, our aim was to promote osteogenic differentiation of human adipose stem cells (hASCs) encapsulated in gellan gum (GG) or collagen type I (COL) hydrogels with bioactive glass (experimental glass 2-06 of composition [wt-%]: Na2O 12.1, K2O 14.0, CaO 19.8, P2O5 2.5, B2O3 1.6, SiO2 50.0) extract based osteogenic medium (BaG OM) for bone construct development. GG hydrogels were crosslinked with spermidine (GG-SPD) or BaG extract (GG-BaG). Methods Mechanical properties of cell-free GG-SPD, GG-BaG, and COL hydrogels were tested in osteogenic medium (OM) or BaG OM at 0, 14, and 21 d. Hydrogel embedded hASCs were cultured in OM or BaG OM fo…

SerumAdipose stem cellCompressive StrengthAdipose tissueCell Count02 engineering and technologySpectrum Analysis Raman01 natural sciencesMineralization (biology)Hydrogel Polyethylene Glycol Dimethacrylatelaw.inventionchemistry.chemical_compoundOsteogenesislawOsteogenic differentiationBioactive glassMineralsTissue ScaffoldsbiologyStem CellsPolysaccharides Bacterialbioactive glassCell DifferentiationMiddle Aged021001 nanoscience & nanotechnologyGellan gumCross-Linking ReagentsAdipose TissueMechanics of MaterialsBioactive glassSelf-healing hydrogelsOsteocalcinFemaleStem cellimplantit0210 nano-technologyMaterials scienceCell SurvivalOsteocalcinosteogenic differentiationchemistry.chemical_elementBioengineeringmacromolecular substancesCalciumta3111010402 general chemistryCollagen Type ICollagen type I hydrogelBiokemia solu- ja molekyylibiologia - Biochemistry cell and molecular biologylasiBiomaterialsCalcification Physiologicbiologinen aktiivisuusgellan gum hydrogelAnimalsHumansta217Ionsgeelitta1182adipose stem cellkantasolutRats0104 chemical sciencesDurapatiteGene Expression RegulationchemistryBiophysicsbiology.proteinGlassGellan gum hydrogelluukudoksetcollagen type I hydrogelBiomarkersMaterials Science and Engineering: C
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Urinary collagen cross-links to evaluate hyperparathyroidism in kidney transplant patients

2008

INTRODUCTION AND AIMS: One of most common complication following kidney transplantation is reappearance of hyperparathyroidism (HP) some months after normal serum levels. An early diagnosis represents the best prophylaxis measures to prevent worsening of osteodystrophy and potential damage to the graft and vascular tissue.The aim to our study was to evaluate, beyond the common HP markers, if the urinary cross-links of the collagen PYD (pyridinoline) and DPD (Deoxypyridinoline) are useful markers able to show increasing levels of parathormone. METHODS: We evaluated 50 stable kidney transplanted patients divided into 2 group (A: 38 pts and B: 12 pts) dependent on the type of their immunosuppr…

Settore MED/18 - Chirurgia Generaleurinary cross-links kidney trasplant patients
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