Search results for "MOLECULAR RECOGNITION"

showing 10 items of 112 documents

The gold-sulfur interface at the nanoscale.

2012

Thiolate-protected gold surfaces and interfaces, relevant for self-assembled monolayers of organic molecules on gold, for passivated gold nanoclusters and for molecule-gold junctions, are archetypal systems in various fields of current nanoscience research, materials science, inorganic chemistry and surface science. Understanding this interface at the nanometre scale is essential for a wide range of potential applications for site-specific bioconjugate labelling and sensing, drug delivery and medical therapy, functionalization of gold surfaces for sensing, molecular recognition and molecular electronics, and gold nanoparticle catalysis. During the past five years, considerable experimental …

Models MolecularChemistrySurface PropertiesGeneral Chemical EngineeringNanoparticleMolecular electronicsNanotechnologyStereoisomerismGeneral ChemistryCrystallography X-RayNanoclustersMolecular recognitionDrug Delivery SystemsMonolayerSurface modificationNanotechnologyNanometreGoldSulfhydryl CompoundsNanoscopic scaleSulfurNature chemistry
researchProduct

Monoester copillar[5]arenes: synthesis, unusual self-inclusion behavior, and molecular recognition.

2012

The self-inclusion behavior of monoester copillar[5]arenes depends on the position of the ester group, which causes different guest selectivities. Monoester copillar[5]arenes bearing an acetate chain can form stable self-inclusion complexes in low- and high-concentration solution and exhibit high guest selectivity. However, a monoester copillar[5]arene bearing a butyrate chain can not form a self-inclusion complex and exhibits low guest selectivity. Thus, a new class of stable self-inclusion complexes of copillar[5]arenes was explored to improve the selectivity of molecular recognition.

Models MolecularMagnetic Resonance SpectroscopyMolecular StructureChemistryStereochemistryOrganic ChemistryMolecular ConformationGeneral ChemistryNuclear magnetic resonance spectroscopyAcetatesCrystallography X-RayCombinatorial chemistryCatalysisMolecular conformationMolecular recognitionMoleculePolycyclic CompoundsHost–guest chemistrySelectivityChemistry (Weinheim an der Bergstrasse, Germany)
researchProduct

DNA minor groove binders: an overview on molecular modeling and QSAR approaches

2007

Molecular recognition of DNA by small molecules and proteins is a fundamental problem in structural biology and drug design. Understanding of recognition in both sequence-selective and sequence neutral ways at the level of successful prediction of binding modes and site selectivity will be instrumental for improvements in the design and synthesis of new molecules as potent and selective gene-regulatory drugs. Minor groove is the target of a large number of non-covalent binding agents. DNA binding with specific sequences, mostly AT, takes place by means of a combination of directed hydrogen bonding to base pair edges, van der Waals interactions with the minor groove walls and generalized ele…

Models MolecularPharmacologyDNA minor groove binders (mGBs) in silico techniques molecular modeling ab initio methods docking molecular dynamics simulations (MDS) QSAR QSPR.Molecular modelBase pairStereochemistryChemistryIn silicoOrganic ChemistryQuantitative Structure-Activity RelationshipDNAComputational biologyBiochemistrySmall moleculechemistry.chemical_compoundMolecular recognitionPharmaceutical PreparationsStructural biologyDocking (molecular)Drug DesignDrug DiscoveryNucleic Acid ConformationMolecular MedicineDNA
researchProduct

Alkali metal mediated resorcarene capsules: An ESI-FTICRMS study on gas-phase structure and cation binding of tetraethyl resorcarene and its per-meth…

2002

AbstractElectrospray ionization Fourier transform ion cyclotron resonance mass spectrometry (ESI-FTICRMS) with additional ab initio calculations were used to examine the alkali metal cation binding selectivity (i.e., molecular recognition) and host properties of tetraethyl resorcarene (1) and its per-methylated derivative (2). The significance of intramolecular hydrogen bonding for the crown conformation was demonstrated. The presence of intramolecular flip-flop hydrogen bonding in 1 was confirmed both with calculations and in ND3-exchange experiments. All the alkali metal cations formed host–guest complexes by docking inside the cavity of the host. Complexation with the larger cations, esp…

Models MolecularSpectrometry Mass Electrospray IonizationCation bindingFourier AnalysisHydrogen bondChemistryStereochemistryElectrospray ionizationMolecular ConformationHydrogen BondingAlkaliesIon cyclotron resonance spectrometryMethylationFourier transform ion cyclotron resonanceMolecular recognitionMetalsStructural BiologyIntramolecular forcePolymer chemistryMoleculePolycyclic CompoundsSpectroscopyJournal of the American Society for Mass Spectrometry
researchProduct

Structural and physicochemical characterization of the inclusion complexes of cyclomaltooligosaccharides (cyclodextrins) with melatonin

2002

The stoichiometry, geometry, stability, and solubility of the inclusion complexes of melatonin (MLT) with native cyclomaltooligosaccharides (α-, β- or γ-cyclodextrins, CDs) are determined experimentally by high-resolution NMR spectroscopy, calorimetric and solubility measurements, and mass spectrometry. The observed differences are discussed in terms of molecular recognition expression of the host-guest (h-g) interactions within the hydrophobic CDs cavities of different size. The 1:1 h-g stoichiometry in water solution prevails at low CD concentrations; the trend to form higher order associations is observed at increasing CD concentrations. The stability order β-CD>γ-CD>α-CD for the c…

Models MolecularSpectrometry Mass Electrospray IonizationElectrospray ionizationProtonationCalorimetryCalorimetryMass spectrometryBiochemistryInclusion complexeAnalytical ChemistryExcipientsMolecular recognitionCyclodextrinSolubilityNuclear Magnetic Resonance BiomolecularMelatoninCyclodextrinsMass spectrometryChemistryOrganic ChemistryGeneral MedicineNuclear magnetic resonance spectroscopyNMRCrystallographySolubilityThermodynamicsStoichiometry
researchProduct

Modeling of the role of conformational dynamics in kinetics of the antigen-antibody interaction in heterogeneous phase.

2012

[EN] A novel approach that may potentially be used to study biomolecular interactions including the simultaneous determination of structural and kinetic binding parameters is described in this Article for the first time. It allows a rigid distinction between the possible reaction mechanisms of biomolecular recognition, induced fit and conformational selection. The relative importance of the two pathways is determined not by comparing rate constants but the structural aspects of the interaction instead. So the exact location of antigen molecules with respect to the capture antibody is depicted experimentally, avoiding the use of X-ray crystallography. The proposed pattern is applied to study…

Models MolecularTime FactorsSimultaneous determinationsProtein ConformationRate constantsBinding processAntigen-Antibody ComplexImmunoglobulin GFragment antigen-bindingConformational dynamicsMiceStructural aspectsBiomolecular recognitionMaterials ChemistrySteric hindrancesBovine serum albuminReaction mechanismbiologyChemistryIn-situSerum Albumin BovineLigand (biochemistry)Reaction schemesSurfaces Coatings and FilmsConformationsAntigen-antibody interactionBovine serum albuminsBiomolecular interactionsMolecular recognitionBSA moleculesAlgorithmsProtein BindingStereochemistryKinetic bindingReaction intermediateAntigen bindingAntibodiesMolecular recognitionAntigenQUIMICA ANALITICAAnimalsComputer SimulationPhysical and Theoretical ChemistryAntigensHeterogeneous phaseInduced fitX ray crystallographyMoleculesSensing surfaceKineticsSilicon chipInterferometryConformational selectionImmunoglobulin Gbiology.proteinBiophysicsCattleAntigen-antibody interactionThe journal of physical chemistry. B
researchProduct

A supramolecular system that strictly follows the binding mechanism of conformational selection

2020

Induced fit and conformational selection are two dominant binding mechanisms in biology. Although induced fit has been widely accepted by supramolecular chemists, conformational selection is rarely studied with synthetic systems. In the present research, we report a macrocyclic host whose binding mechanism is unambiguously assigned to conformational selection. The kinetic and thermodynamic aspects of this system are studied in great detail. It reveals that the kinetic equation commonly used for conformational selection is strictly followed here. In addition, two mathematical models are developed to determine the association constants of the same guest to the two host conformations. A “confo…

Models Molecularconformational selectionProtein ConformationScienceSupramolecular chemistrybiological systemsGeneral Physics and Astronomy010402 general chemistryLigands01 natural sciencesGeneral Biochemistry Genetics and Molecular BiologyBiophysical PhenomenaArticlesupramolecular chemistryMolecular recognitionProtein structureProtein DomainsComputational chemistryHeterocyclic Compoundsmechanisms in biologysupramolekulaarinen kemialcsh:ScienceSelection (genetic algorithm)Multidisciplinary010405 organic chemistryMechanism (biology)QProteinsGeneral ChemistryModels Theoretical0104 chemical sciencesKineticsPhysical chemistryKinetic equationsProteins metabolismsynthetic systemsThermodynamicslcsh:Qmolecular recognitionSupramolecular chemistryProtein Binding
researchProduct

The Role of Side-Arms for Supramolecular Affinity Materials Based on 9,9′-Spirobifluorenes

2017

An eightfold functionalized D2d-symmetric 9,9' spirobifluorene was condensed with a collection of diketones with elaborated structural features to form three-dimensional supramolecular architectures with active surfaces. Gas sorption measurements by quartz crystal microbalances revealed remarkable indications about the molecular interactions for the application as affinity materials for the detection of volatile organic compounds. Single-crystal X-ray structure analysis further gave insight by packing motifs and for potential host-guest interactions.

Molecular interactionsStructure analysis010405 organic chemistryChemistryOrganic ChemistrySupramolecular chemistrySorption010402 general chemistry01 natural sciences0104 chemical sciencesCrystalMolecular recognitionComputational chemistryOrganic chemistryPhysical and Theoretical ChemistryQuartzEuropean Journal of Organic Chemistry
researchProduct

Use of Bile Acids in Pharmacological and Supramolecular Applications

2004

Bile acid-based structures have become increasingly important in different fields of chemistry over recent years, having found applications in pharmacology, supramolecular chemistry and nanoscience. Some interesting studies concerning these applications are reviewed, together with the latest developments in synthetic and analytical methods for bile acid-derived frameworks. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004)

Molecular recognitionBiochemistryBile acidmedicine.drug_classChemistryOrganic ChemistrySupramolecular chemistrymedicineNanotechnologyGeneral MedicinePhysical and Theoretical ChemistryCombinatorial chemistryChemInform
researchProduct

Self-assembly of amphiphilic calixarenes and resorcinarenes in water

2010

The calixarenes and resorcinarenes are macrocyclic phenolic molecules that can be modified “a facon” and a wide range of chemical modification strategies have been published over the last 30 years. Because of their remarkable structural properties and their relative ease of chemical modification, they represent excellent and highly versatile bases to design complex building blocks capable of self-assembly and molecular recognition. They have been widely studied for their ability to form supramolecular structures targeting a wide range of applications. The possibility to regio(rim)-selectively modify these macrocycles with different polar and apolar moieties provides synthetic chemists with …

Molecular recognitionChemistryAmphiphileCalixareneMaterials ChemistrySupramolecular chemistryChemical modificationMoleculeNanotechnologyGeneral ChemistrySelf-assemblyCatalysisNew Journal of Chemistry
researchProduct