Search results for "isothermal titration calorimetry"

showing 10 items of 51 documents

Mg2+ binding triggers rearrangement of the IM30 ring structure, resulting in augmented exposure of hydrophobic surfaces competent for membrane binding

2018

The "inner membrane-associated protein of 30 kDa" (IM30), also known as "vesicle-inducing protein in plastids 1" (Vipp1), is found in the majority of photosynthetic organisms that use oxygen as an energy source, and its occurrence appears to be coupled to the existence of thylakoid membranes in cyanobacteria and chloroplasts. IM30 is most likely involved in thylakoid membrane biogenesis and/or maintenance, and has recently been shown to function as a membrane fusion protein in presence of Mg2+ However, the precise role of Mg2+ in this process and its impact on the structure and function of IM30 remains unknown. Here, we show that Mg2+ binds directly to IM30 with a binding affinity of ∼1 mm …

0301 basic medicineMembrane fusion proteinChemistryPspALipid bilayer fusionIsothermal titration calorimetryMg2+Cell BiologyBiochemistry[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistry03 medical and health sciences030104 developmental biologyThylakoidMembrane biogenesisBiophysicsFourier transform IREnergy sourceMolecular BiologyMembrane biophysicsIM30BiogenesisJournal of Biological Chemistry
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Biopolymer-Targeted Adsorption onto Halloysite Nanotubes in Aqueous Media.

2017

Studies on the adsorption of biopolymers onto halloysite nanotubes (HNTs) in water were conducted. Three polymers with different charges-anionic (pectin), neutral (hydroxypropyl cellulose), and cationic (chitosan)-were chosen. The thermodynamic parameters for the adsorption of polymers onto the HNT surface were determined by isothermal titration calorimetry (ITC). The experimental data were interpreted based on a Langmuir adsorption model. The standard variations in free energy, enthalpy, and entropy of the process were obtained and discussed. Turbidimetry was used to evaluate the stability of functionalized nanoparticles in water. The ζ-potential clarified the surface charge properties of …

Materials scienceBiopolymerFunctionalized nanotube02 engineering and technologyengineering.materialHydroxypropyl cellulose010402 general chemistry01 natural sciencesHalloysitechemistry.chemical_compoundsymbols.namesakeAdsorptionEnthalpyKaoliniteLangmuir adsorption modelPolymer chemistryElectrochemistryHalloysite nanotube (HNTs)General Materials ScienceSurface chargeFree energyPolymerSpectroscopyYarn Functionalized nanoparticleHydroxypropyl celluloseLangmuir adsorption modelWaterIsothermal titration calorimetrySurfaces and InterfacesPolymer adsorptionThermal Propertie021001 nanoscience & nanotechnologyCondensed Matter PhysicsPectin0104 chemical sciencesBiomoleculeNanotubechemistryChemical engineeringengineeringsymbolsIsothermal titration calorimetryBiopolymerAdsorption0210 nano-technologySurface charge propertieThermodynamic parameter Polymers ChitosanLangmuir : the ACS journal of surfaces and colloids
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Analysis of substrate binding in individual active sites of bifunctional human ATIC

2018

Aminoimidazolecarboxamide ribonucleotide formyl transferase (AICARFT): Inosine monophosphate cyclohydrolase (IMPCH, collectively called ATIC) is a bifunctional enzyme that catalyses the penultimate and final steps in the purine de novo biosynthesis pathway. The bifunctional protein is dimeric and each monomer contains two different active sites both of which are capable of binding nucleotide substrates, this means to a potential total of four distinct binding events might be observed. Within this work we used a combination of site-directed and truncation mutants of ATIC to independently investigate the binding at these two sites using calorimetry. A single S10W mutation is sufficient to blo…

0301 basic medicineHydroxymethyl and Formyl TransferasesModels MolecularRibonucleotideStereochemistryBiophysicsBiochemistryAnalytical ChemistrySubstrate Specificity03 medical and health scienceschemistry.chemical_compoundMultienzyme ComplexesCatalytic DomainTransferaseHumansNucleotidePhosphofructokinase 2Bifunctional enzymesMolecular Biologychemistry.chemical_classification030102 biochemistry & molecular biologybiologyNucleotidesActive siteCooperative bindingIsothermal titration calorimetryXanthosine monophosphate030104 developmental biologyBiochemistrychemistryNucleotide DeaminasesMultiple binding sitesbiology.proteinIsothermal titration calorimetryProtein Binding
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Structure of SNX9 SH3 in complex with a viral ligand reveals the molecular basis of its unique specificity for alanine-containing class I SH3 motifs

2021

Class I SH3 domain-binding motifs generally comply with the consensus sequence [R/K]x0PxxP, the hydrophobic residue 0 being proline or leucine. We have studied the unusual 0 = Ala-specificity of SNX9 SH3 by determining its complex structure with a peptide present in eastern equine encephalitis virus (EEEV) nsP3. The structure revealed the length and composition of the n-Src loop as important factors determining specificity. We also compared the affinities of EEEV nsP3 peptide, its mutants, and cellular ligands to SNX9 SH3. These data suggest that nsP3 has evolved to minimize reduction of conformational entropy upon binding, hence acquiring stronger affinity, enabling takeover of SNX9. The R…

DYNAMICSPROLINE-RICH PEPTIDESviruksetPROTEINSvirusesHTLV-1 GagLigandsEVOLUTIONARY CONSERVATIONalfaviruksetsrc Homology DomainsHIGH-AFFINITYretroviruksetDOMAINStructural BiologyBINDINGAnimalsHorsesMolecular Biologysoluviestintä11832 Microbiology and virologyAlanineBinding SitesPXXP MOTIFSisothermal titration calorimetrySH3solution NMR spectroscopyEEEV nsP3HIV-11182 Biochemistry cell and molecular biologyproteiinitCHEMICAL-SHIFTS3111 BiomedicinePeptidesSNX9Protein Binding
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Cytotoxic hydrophilic iminophosphorane coordination compounds of d8 metals. Studies of their interactions with DNA and HSA

2012

The synthesis and characterization of a new water-soluble N,N-chelating iminophosphorane ligand TPAN-C(O)-2-NC(5)H(4) (N,N-IM) (1) and its d(8) (Au(III), Pd(II) and Pt(II)) coordination complexes are reported. The structures of cationic [AuCl(2)(N,N-IM)]ClO(4) (2) and neutral [MCl(2)(N,N-IM)] M=Pd (3), Pt(4) complexes were determined by X-ray diffraction studies or by means of density-functional calculations. While the Pd and Pt compounds are stable in mixtures of DMSO/H(2)O over 4 days, the gold derivative (2) decomposes quickly to TPAO and previously reported neutral gold(III) compound [AuCl(2)(N,N-H)] 5 (containing the chelating N,N-fragment HN-C(O)-2-NC(5)H(4)). The cytotoxicities of co…

Circular dichroismMagnetic Resonance SpectroscopyStereochemistryPhosphoranesAntineoplastic AgentsBiochemistryMedicinal chemistryArticleCoordination complexInorganic ChemistryX-Ray DiffractionCell Line TumorSpectroscopy Fourier Transform InfraredmedicineHumansChelationSerum Albuminchemistry.chemical_classificationCisplatinLigandCircular DichroismIsothermal titration calorimetryDNANuclear magnetic resonance spectroscopyHuman serum albuminSpectrometry FluorescencechemistryMetalsCisplatinHydrophobic and Hydrophilic Interactionsmedicine.drugJournal of Inorganic Biochemistry
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Binding abilities of new cyclodextrin-cucurbituril supramolecular hosts

2015

Various combined techniques (UV–vis spectrophotometry, isothermal titration calorimetry, thermogravimetry, ESI-MS mass spectrometry, polarimetry and 1H NMR spectroscopy) were used in order to study the interaction between a new combined supramolecular host, namely a bow-tie-structured cyclodextrin–cucurbituril association solely held by non-covalent interactions, and a suitably selected guest, namely the N-(p-nitrophenyl)-1,8-diaminooctane hydrochloride. In particular, the use of different techniques highlighted the peculiar features of the possible host–guest supramolecular interactions under different concentration conditions.

chemistry.chemical_classificationcucubiturilCyclodextrinsmedicine.diagnostic_testCyclodextrinHydrochloridecucurbiturilsSupramolecular chemistryIsothermal titration calorimetryGeneral ChemistrySettore CHIM/06 - Chimica OrganicaMass spectrometrycucurbiturilThermogravimetryCrystallographychemistry.chemical_compoundcyclodextrinchemistryComputational chemistryCucurbiturilSpectrophotometrymedicinecucurbiturils; Cyclodextrins; supramolecular co-polymerssupramolecular co-polymerscyclodextrins; cucurbiturils; supramolecular co-polymers
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PAA-PAMPS Copolymers as an Efficient Tool to Control CaCO3 Scale Formation

2013

Scale formation, the deposition of certain minerals such as CaCO3, MgCO3, and CaSO4 center dot 2H(2)O in industrial facilities and household devices, leads to reduced efficiency or severe damage. Therefore, incrustation is a major problem in everyday life. In recent years, double hydrophilic block copolymers (DHBCs) have been the focus of interest in academia with regard to their antiscaling potential. In this work, we synthesized well-defined blocklike PAA-PAMPS copolymers consisting of acrylic acid (AA) and 2-acrylamido-2-methyl-propane sulfonate (AMPS) units in a one-step reaction by RAFT polymerization. The derived copolymers had dispersities of 1.3 and below. The copolymers have then b…

Materials sciencePolymersPotentiometric titrationAcrylic ResinsMicroscopy Atomic Force530Calcium Carbonatelaw.inventionchemistry.chemical_compoundlawPolymer chemistryElectrochemistryCopolymerChemical PrecipitationGeneral Materials ScienceReversible addition−fragmentation chain-transfer polymerizationCrystallizationSpectroscopyAcrylic acidchemistry.chemical_classificationWaterIsothermal titration calorimetrySurfaces and InterfacesPolymerCondensed Matter PhysicsPolyelectrolytechemistrySulfonic AcidsCrystallization
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Thermodynamic analysis of binding between drugs and glycosaminoglycans by isothermal titration calorimetry and fluorescence spectroscopy

2007

The thermodynamics of the interaction of positively charged drug molecules with negatively charged glycosaminoglycans (GAGs) is investigated by isothermal titration calorimetry (ITC) and fluorescence spectroscopy. The drugs considered are propranolol hydrochloride, tacrine, and aminacrine, and the polymers used as model GAGs are dextran sulfate, chondroitin sulfate, and hyaluronic acid. The ITC results show that the interaction between drugs and GAGs is via direct binding and that GAGs bind to drugs at one set of sites. Large negative values of heat capacity change (DeltaC(p)) are observed upon binding of GAGs to drugs. Such negative DeltaC(p) is not expected for purely electrostatic intera…

CarbohydratesFluorescence spectrometryPharmaceutical ScienceCalorimetryCalorimetryFluorescence spectroscopychemistry.chemical_compoundChondroitin sulfateHyaluronic AcidFluorescent DyesGlycosaminoglycansLiaisonChemistryChondroitin SulfatesTemperatureProteinsMembranes ArtificialIsothermal titration calorimetryHydrogen-Ion ConcentrationPropranololAminacrineSpectrometry FluorescenceMembranePharmaceutical PreparationsBiochemistryDrug deliveryTacrineBiophysicsThermodynamicsIndicators and ReagentsEuropean Journal of Pharmaceutical Sciences
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Aqueous phase/nanoparticles interface: hydroxypropyl cellulose adsorption and desorption triggered by temperature and inorganic salts

2012

The study highlighted the main forces driving the adsorption of hydroxypropyl cellulose (HPC) onto clay nanoparticles with a disk-like shape (Laponite RD). Modeling the isothermal titration calorimetry data provided the key thermodynamic properties, which enabled us to discuss the microscopic aspects contributing to the energetic and the entropic changes of the polymer adsorption at the nanoparticle/liquid interface. We evidenced that the process is strongly enthalpy-driven and that the interactions lead to constraints of the HPC configuration at interface. The functionalized nanoparticles enhanced the polymer solubility in water expanding the one-phase area of the binodal curve. Temperatur…

BinodalMaterials scienceHydroxypropyl cellulosenanoparticles interface cellulose calorimetryNanoparticleIsothermal titration calorimetryGeneral ChemistryPolymer adsorptionCondensed Matter Physicschemistry.chemical_compoundAdsorptionchemistryChemical engineeringDesorptionOrganic chemistrySolubilitySettore CHIM/02 - Chimica Fisica
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Efficient stabilisation of a dihydrogenphosphate tetramer and a dihydrogenpyrophosphate dimer by a cyclic pseudopeptide containing 1,4-disubstituted …

2017

A cyclic pseudooctapeptide 2 is described containing 1,4-disubstituted 1,2,3-triazole moieties. This compound features eight converging hydrogen bond donors along the ring, namely four amide NH and four triazole CH groups, which enable 2 to engage in interactions with anions. While fully deprotonated sulfate anions exhibit only moderate affinity for 2, protonated anions such as dihydrogenpyrophosphate and dihydrogenphosphate anions are strongly bound. Complexation of the phosphate-derived anions involves sandwiching of a dihydrogenpyrophosphate dimer or a dihydrogenphosphate tetramer between two pseudopeptide rings. X-ray crystallography provided structural information, while 1H NMR spectro…

fosfaatit010405 organic chemistryStereochemistryChemistryHydrogen bondDimerTriazoleIsothermal titration calorimetryProtonationGeneral Chemistry010402 general chemistry01 natural sciencesphosphate oligomers0104 chemical sciencesoligomeeriCrystallographychemistry.chemical_compoundDeprotonationpseudopeptidesTetramerAmidestabilisationta116orgaaniset yhdisteetChemical Science
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