Search results for "serum albumin"

showing 10 items of 283 documents

The deubiquitinase USP11 is a versatile and conserved regulator of autophagy

2021

Autophagy is a major cellular quality control system responsible for the degradation of proteins and organelles in response to stress and damage to maintain homeostasis. Ubiquitination of autophagy-related proteins or regulatory components is important for the precise control of autophagy pathways. Here, we show that the deubiquitinase ubiquitin-specific protease 11 (USP11) restricts autophagy and that KO of USP11 in mammalian cells results in elevated autophagic flux. We also demonstrate that depletion of the USP11 homolog H34C03.2 in Caenorhabditis elegans triggers hyperactivation of autophagy and protects the animals against human amyloid-β peptide 42 aggregation-induced paralysis. USP11…

autophagyhAβ42 human amyloid-β protein 1 to 42Lipid kinase activityPI(3)P phosphatidylinositol-3-phosphatemTORC1BiochemistryCell LineGene Knockout Techniqueschemistry.chemical_compoundubiquitinAnimalsHumansULK1 unc-51-like autophagy activating kinase 1WIPI WD-repeat domain phosphoinositide-interacting proteinPI3KC3-C1Caenorhabditis elegansCaenorhabditis elegans ProteinsmTORC1Molecular BiologyMechanistic target of rapamycinUSP11 ubiquitin-specific protease 11proteostasisAmyloid beta-PeptidesS6K S6 kinasebiologyPhosphatidylinositol 3-phosphateAutophagyDUB deubiquitinaseLFQ label-free quantificationIP immunoprecipitationNHT nonhuman targetingPI3KC3-C1 class III phosphatidylinositol 3-kinase complex ICell BiologyACN acetonitrile amyloid-βNRBF2 nuclear receptor-binding factor 2Peptide FragmentsCell biologydeubiquitinase (DUB)ProteostasischemistryProteotoxicitymTORC1 mechanistic target of rapamycin complex 1biology.proteinAutophagy-Related Protein-1 HomologBSA bovine serum albuminThiolester HydrolasesResearch ArticleJournal of Biological Chemistry
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Thermal aggregation of proteins in presence of metal ions.

2008

The study of the aggregation processes in presence of metal ions is an essential step for understanding the key role of metals in protein-protein and protein-solvent interactions. Indeed, the presence of metal ions can radically change the main features of the standard denaturation/aggregation processes and such effects result to be strongly dependent on the kind of metal and on its concentration. Metal ions have an active role in thermal aggregation and cold set gelation processes. These processes are intrinsically different, but both are based on the proteins ability to form aggregates.

beta-LactoglobulinBovine Serum AlbuminProteins aggregation processeMetal IonConformational changeSettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)
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Spectroscopic studies of water-soluble superstructured iron(III) porphyrin. Interaction with the bovine serum albumin protein

2018

Acid-base equilibrium of the “one-face”-hindered sulfonated porphyrin, α5,15-[2,2′(dodecamethyleneoxy),(5-sulfonato)diphenyl]-10,20-bis(2-hydroxy,5-sulfonatophenyl)porphyrinato iron(III), has been ...

biologyAlbumin02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesPorphyrin0104 chemical scienceslaw.inventionchemistry.chemical_compoundWater solublechemistrylawMaterials Chemistrybiology.proteinPhysical and Theoretical ChemistryBovine serum albumin0210 nano-technologyElectron paramagnetic resonanceNuclear chemistryJournal of Coordination Chemistry
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Drug Binding Properties of Tyrosine-Modified Human Serum Albumin

1978

Human serum albumin (HSA) has only a small number of specific binding sites for drugs. There are facts indicating that tyrosine residues may be involved in these binding sites. Thus we modified HSA with tetranitromethan, a reagent specific for tyrosine residues in proteins. As derived from an UV-absorption quotient three albumins with a degree of modification of two, five and eight residues per molecule were obtained. Only for the albumin with eight residues modified a small reduction of ordered secondary structure was found.

biologyChemistryAlbuminSerum albuminPlasma protein bindingHuman serum albuminBiochemistrybiology.proteinmedicineBinding siteTyrosineBovine serum albuminProtein secondary structuremedicine.drug
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Protein transport through gold-coated, charged nanopores: Effects of applied voltage

2006

The flux of bovine serum albumin and bovine hemoglobin through charged nanopores inside polymeric membranes is analysed as a function of the applied voltage to the nanopore surface, the solution ionic strength and pH. The electrostatic interaction of the protein with the nanopore surface gives low transport rates except at the protein isoelectric point and the minimum of the effective, voltage-induced nanopore charge. This electrostatic sieving effect allows for the separation of proteins with similar molecular weights.

biologyChemistryAnalytical chemistryGeneral Physics and AstronomyFluxTransport proteinNanoporeIsoelectric pointChemical engineeringIonic strengthbiology.proteinPhysical and Theoretical ChemistryBovine serum albuminPolymeric membraneVoltageChemical Physics Letters
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Surface Modification of Porous Polyethylene Implants with an Albumin-Based Nanocarrier-Release System

2021

Background: Porous polyethylene (PPE) implants are used for the reconstruction of tissue defects but have a risk of rejection in case of insufficient ingrowth into the host tissue. Various growth factors can promote implant ingrowth, yet a long-term gradient is a prerequisite for the mediation of these effects. As modification of the implant surface with nanocarriers may facilitate a long-term gradient by sustained factor release, implants modified with crosslinked albumin nanocarriers were evaluated in vivo. Methods: Nanocarriers from murine serum albumin (MSA) were prepared by an inverse miniemulsion technique encapsulating either a low- or high-molar mass fluorescent cargo. PPE implants …

biologyChemistryQH301-705.5release kineticsSerum albuminbiomaterialMedicine (miscellaneous)Biomaterialfluorescence microscopyGeneral Biochemistry Genetics and Molecular BiologyArticlematerial scienceMiniemulsionTissue engineeringIn vivoporous polyethylenetissue engineeringbiology.proteinSurface modificationImplantNanocarriersBiology (General)dorsal skinfold chamberalbumin nanocarriersBiomedical engineeringBiomedicines
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Action de la chlorhexidine sur l'expression de la virulence de

1999

Abstract Candida albicans is an opportunistic yeast. Its pathogenicity is linked to the susceptibility of the host surface as well as to particular factors of the strain: adhesion, filamentous growth and secretion of proteolytic enzymes. Chlorhexidine digluconate is an antiseptic with fungicidal properties. The action of the antiseptic on the growth of the yeast shows a minimal inhibitory concentration (MIC) at 50 μg·mL−1 and a minimal fungicidal concentration (MFC) at 100 μg·mL−1. The consequences of antiseptic treatment are studied using two indicators of pathogenicity: filamentation and the secretion of acid proteinase. Concerning the morphological indicator, a complete inhibition of fil…

biologymedicine.drug_classChlorhexidineProteolytic enzymesbiology.organism_classificationYeastMicrobiologyMinimum inhibitory concentrationAntisepticBiochemistryCaseinmedicinebiology.proteinBovine serum albuminCandida albicansEcology Evolution Behavior and Systematicsmedicine.drugCryptogamie Mycologie
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Joint Aqueous Solutions of Dextran and Bovine Serum Albumin: Coexistence of Three Liquid Phases

2014

The phase diagram of the system water/dextran (DEX)/BSA was measured as well as modeled. On the experimental side, cloud points were determined and the coexisting phases were analyzed. The theoretical calculations use an approach capable of describing solutions of chain polymers and of globular proteins with the same formalism. The required thermodynamic input comes from experiments concerning the binary subsystems, except for the polymer blend for which one interaction parameter had to be adjusted. Both sources of information yield the same essential features: the existence of a large composition area of immiscibility, starting from the subsystem DEX/BSA and extending well into the region …

chemistry.chemical_classificationAqueous solutionbiologyPolymersGlobular proteinAnalytical chemistryDextransSerum Albumin BovineSurfaces and InterfacesPolymerFlory–Huggins solution theoryCondensed Matter PhysicsSolutionschemistry.chemical_compoundDextranchemistryElectrochemistrybiology.proteinAnimalsCattleGeneral Materials SciencePolymer blendBovine serum albuminSpectroscopyPhase diagramLangmuir
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Liquid/Gas and Liquid/Liquid Phase Equilibria of the System Water/Bovine Serum Albumin

2013

The thermodynamic behavior of the system H2O/BSA was studied at 25 °C within the entire composition range: vapor pressure measurements via head space sampling gas chromatography demonstrate that the attainment of equilibria takes more than one week. A miscibility gap was detected via turbidity and the coexisting phases were analyzed. At 6 °C the two phase region extends from ca. 34 to 40 wt % BSA; it shrinks upon heating. The polymer rich phase is locally ordered, as can be seen under the optical microscope using crossed polarizers. The Flory-Huggins theory turns out to be inappropriate for the modeling of experimental results. A phenomenological expression is employed which uses three adju…

chemistry.chemical_classificationChromatography GasChemistrySpinodal decompositionVapor pressureLiquid gasAnalytical chemistryWaterSerum Albumin BovinePolymerPolarizerSurfaces Coatings and Filmslaw.inventionOptical microscopelawPhase (matter)Materials ChemistryAnimalsThermodynamicsCattleGas chromatographyPhysical and Theoretical ChemistryThe Journal of Physical Chemistry B
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Selective extraction of small proteins from biological samples using a novel restricted access column with cation exchange properties

2000

The determination of proteins utilising a polymer-based restricted access suppor material with ion exchange properties (IERAM) is outlined. Solid phase extraction coupled on-line with a mincrobore reversed phase HPLC system for the quantitation of small marker proteins is demonstrated. The cation-exchange restricted access packings were characterised with respect to their adsorption and desorption kinetics. The IERAM material was also investigated by capacity, selectivity, and biocompatibility determinations when applied to the quantification of small molecular weight proteins such as cytochrome C, Lysozyme, Ribonuclease A, Myoglobin, Insulin, human serum albumin, and a Tryptic inhibitor.

chemistry.chemical_classificationChromatographyIon exchangebiologyChemistryOrganic ChemistryClinical BiochemistryExtraction (chemistry)PolymerReversed-phase chromatographyHuman serum albuminBiochemistryAnalytical ChemistryMatrix-assisted laser desorption/ionizationmedicinebiology.proteinPancreatic ribonucleaseSolid phase extractionmedicine.drug
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