Search results for "hydrogen bonding"

showing 10 items of 290 documents

Molecular dynamics, dynamic site mapping, and highthroughput virtual screening on leptin and the Ob receptor as anti-obesity target.

2014

Body weight control is a mechanism finely regulated by several hormonal, metabolic, and nervous pathways. The leptin receptor (Ob-R) is crucial for energy homeostasis and regulation of food uptake. Leptin is a 16 kDa hormone that is mainly secreted by fat cells into the bloodstream, and under normal circumstances, circulating levels are proportionate to the fat body mass. Sensing of elevated leptin levels by the hypothalamic neurocircutry activates a negative feedback loop resulting in reduced food intake and increased energy expenditure. Decreased concentrations lead to opposite effects. Therefore rational design of leptin agonists constitute an appealing challenge in the battle against ob…

Leptinmedicine.medical_specialtyProtein ConformationAdipose tissueDrug designBiologyMolecular Dynamics SimulationDynamic SiteMapping HTVS Leptin Molecular Dynamics Obesity Protein/protein docking Multivariate analysis Ob ReceptorCatalysisEnergy homeostasisInorganic ChemistryStructure-Activity RelationshipInternal medicinemedicineMolecular Targeted TherapyPhysical and Theoretical ChemistryReceptorVirtual screeningLeptin receptorBinding SitesMolecular StructureLeptindigestive oral and skin physiologyOrganic ChemistryHydrogen BondingSettore CHIM/08 - Chimica FarmaceuticaComputer Science ApplicationsHigh-Throughput Screening AssaysMolecular Docking SimulationEndocrinologyComputational Theory and MathematicsDocking (molecular)Drug DesignMultivariate AnalysisComputer-Aided DesignReceptors LeptinAnti-Obesity AgentsHydrophobic and Hydrophilic InteractionsProtein BindingJournal of molecular modeling
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Is the Rigidity of SARS-CoV-2 Spike Receptor-Binding Motif the Hallmark for Its Enhanced Infectivity? Insights from All-Atom Simulations

2020

The severe acute respiratory syndrome coronavirus (SARS-CoV-2) pandemic is setting the global health crisis of our time, causing a devastating societal and economic burden. An idiosyncratic trait of coronaviruses is the presence of spike glycoproteins on the viral envelope, which mediate the virus binding to specific host receptor, enabling its entry into the human cells. In spite of the high sequence identity of SARS-CoV-2 with its closely related SARS-CoV emerged in 2002, the atomic-level determinants underlining the molecular recognition of SARS-CoV-2 to the angiotensin-converting enzyme 2 (ACE2) receptor and, thus, the rapid virus spread into human body, remain unresolved. Here, multi-m…

LettervirusesAmino Acid MotifsPneumonia ViralVirus Attachment02 engineering and technologyPlasma protein bindingBiologyPeptidyl-Dipeptidase AMolecular Dynamics SimulationVirus03 medical and health sciencesBetacoronavirusViral ProteinsProtein structureViral envelopeGlobal healthHumansGeneral Materials SciencePhysical and Theoretical ChemistryReceptorProtein Structure QuaternaryPandemics030304 developmental biologyGlycoproteinschemistry.chemical_classificationGeneticsInfectivity0303 health sciencesSARS-CoV-2virus diseasesCOVID-19Hydrogen Bonding021001 nanoscience & nanotechnologySARS VirusProtein Structure TertiarySevere acute respiratory syndrome-related coronaviruschemistrySettore CHIM/03 - Chimica Generale E InorganicaQuantum TheoryAngiotensin-Converting Enzyme 20210 nano-technologyGlycoproteinCoronavirus InfectionsProtein Binding
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Halogenido ligand exchange synthesis, spectroscopic properties and thermal behaviour of the inorganic–organic hydrogen-bonded network solid [4,4′-H2b…

2014

Abstract Dark-red single crystals of 4,4′-bipyridinium triaquahydrogen(1+) hexabromidorhodate(III) [4,4′-H2bipy][H7O3][RhBr6] (1) have been synthesized by a diffusion-controlled ligand exchange process from rhodium(III) chloride trihydrate and 4,4′-bipyridine dissolved in hydrochloric and hydrobromic acid, respectively. 1 could be considered as an inorganic–organic hydrogen-bonded network solid built up from the inorganic isolated hexabromidorhodate [RhBr6]3− octahedra, organic 4,4′-bipyridinium(2+) [4,4′-H2bipy]2+ and triaquahydrogen(1+) [H7O3]+ cations with nearly symmetrical O⋯O distances. The oppositely charged components in the structure of 1 are bound together by an intricate system o…

LigandHydrogen bondChemistryIonic bondingchemistry.chemical_elementCrystal structureRhodiumInorganic Chemistrychemistry.chemical_compoundCrystallographyOctahedronMaterials ChemistryDiffusion-controlled reaction; Hybrid materials; Hexahalogenidorhodates(III); Hydrogen bonding; Dehydration; DehydrobrominationOrganic chemistryHydrobromic acidPhysical and Theoretical ChemistryHybrid materialPolyhedron
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Excitation-Wavelength-Dependent Photocycle Initiation Dynamics Resolve Heterogeneity in the Photoactive Yellow Protein from Halorhodospira halophila

2018

Photoactive yellow proteins (PYPs) make up a diverse class of blue-light-absorbing bacterial photoreceptors. Electronic excitation of the p-coumaric acid chromophore covalently bound within PYP results in triphasic quenching kinetics; however, the molecular basis of this behavior remains unresolved. Here we explore this question by examining the excitation-wavelength dependence of the photodynamics of the PYP from Halorhodospira halophila via a combined experimental and computational approach. The fluorescence quantum yield, steady-state fluorescence emission maximum, and cryotrapping spectra are demonstrated to depend on excitation wavelength. We also compare the femtosecond photodynamics …

LightKineticsQuantum yieldMolecular Dynamics Simulation010402 general chemistryPhotochemistryPhotoreceptors Microbial01 natural sciencesBiochemistry/dk/atira/pure/sustainabledevelopmentgoals/life_below_waterStructure-Activity RelationshipBacterial Proteins0103 physical sciencesSDG 14 - Life Below Waterta116Photoactive Yellow ProteinsQuenching (fluorescence)ta114010304 chemical physicsChemistryHalorhodospira halophilaHydrogen BondingChromophoreFluorescence0104 chemical sciencesHalorhodospira halophilaFemtosecondExcitationBiochemistry
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Light-Induced Protein-Matrix Uncoupling and Protein Relaxation in Dry Samples of Trehalose-Coated MbCO at Room Temperature

2005

In humid samples of trehalose-coated carboxy-myoglobin (MbCO), thermally driven conformational relaxation takes place after photodissociation of the carbon monoxide (CO) molecule at room temperature. In such samples, because of the extreme viscosity of the external matrix, photodissociated CO cannot diffuse out of the protein and explores the whole (proximal and distal side) heme pocket, experiencing averaged protein heme pocket structures, as a result of the presence of Brownian motions. At variance, in very dry samples, a lower portion of the photodissociated CO diffuses from the distal to the proximal heme pocket side probing in nonaveraged structures. We revisit here the flash photolysi…

LightProtein ConformationBiophysicsBiochemistrychemistry.chemical_compoundProtein structureAnimalsHumansHemePhotolysisMyoglobinHydrogen bondLasersPhotodissociationRelaxation (NMR)TrehaloseHydrogen BondingCell BiologyGeneral MedicineProtein Structure TertiaryCrystallographychemistryMyoglobinFlash photolysisProtein BindingCarbon monoxideCell Biochemistry and Biophysics
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Photoactivation of Drosophila melanogaster cryptochrome through sequential conformational transitions

2019

Time-resolved x-ray scattering reveals light-induced signal transduction in insect cryptochromes.

LightProtein ConformationSpectrum AnalysisbanaanikärpänenSciAdv r-articlesfotobiologiaHydrogen BondingHydrogen-Ion ConcentrationMolecular Dynamics SimulationBiochemistryModels BiologicalCryptochromesStructure-Activity RelationshipDrosophila melanogasterCatalytic DomainAnimalsproteiinitResearch ArticlesvuorokausirytmiResearch ArticleSignal TransductionScience Advances
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On the chemiluminescence emission of luminol: protic and aprotic solvents and encapsulation to improve the properties in aqueous solution.

2020

Luminol is a popular molecule that is currently gaining further interest due to its potential role for non-invasive cancer treatments. Design of more efficient derivatives in this context would benefit from a clear knowledge on the origin of the distinct intensity and spectroscopic properties in protic and aprotic solvents observed experimentally, which are still not rationalized. By efficiently combining molecular dynamics, quantum methodologies based on density functional theory and multiconfigurational quantum chemistry and hybrid approaches, and developing herein a computational approach for accurately determining "molar negative extinction (or gain) coefficients of emission", we firstl…

LuminescencePhthalic AcidsGeneral Physics and AstronomyMolecular Dynamics Simulation010402 general chemistryPhotochemistry01 natural sciencesQuantum chemistryMolecular electronic transitionLuminollaw.inventionchemistry.chemical_compoundlaw0103 physical sciencesMoleculeDimethyl SulfoxidePhysical and Theoretical ChemistryDensity Functional TheoryChemiluminescenceAqueous solutionLuminescent Agents010304 chemical physicsWaterHydrogen Bonding0104 chemical scienceschemistryModels ChemicalSolventsDensity functional theoryLuminolLuminescencePhysical chemistry chemical physics : PCCP
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Zn(II)-coordination and fluorescence studies of a new polyazamacrocycle incorporating 1H-pyrazole and naphthalene units.

2010

The synthesis and Zn(2+) coordination properties of a new macrocycle (L1) obtained by dipodal (2 + 2) condensation of the polyamine 3-(naphthalen-2-ylmethyl)pentane-1,5-diamine with 1H-pyrazole-3,5-dicarbaldehyde are reported. pH-metric studies show that L1 bears five measurable protonation steps in the 2.0-11.0 pH range. Fluorescence emission studies indicate that the removal of the first proton from the H(5)L1(5+) species leads to a significant decrease in the emission due to a photoinduced electron transfer process. Addition of Zn(2+) promotes a boat-like conformation that approaches both fluorophores and facilitates the formation of an excimer which reaches its highest emission for a 1 …

Macrocyclic CompoundsMolecular ConformationProtonationPyrazoleNaphthalenesPhotochemistryExcimerPhotoinduced electron transferFluorescenceInorganic Chemistrychemistry.chemical_compoundOrganometallic CompoundsPolyaminesMoietyFluorescent DyesMolecular StructureChemistryHydrogen bondHydrogen BondingElectrochemical TechniquesHydrogen-Ion ConcentrationFluorescenceZincPyrazolesDensity functional theoryProtonsCopperDalton transactions (Cambridge, England : 2003)
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Guest exchange in dimeric capsules formed by tetra-urea calix[4]arenes

2008

Ten tetra-urea calix[4]arene derivatives with different ether residues (methyl, pentyl, benzyl, all combinations of methyl and pentyl, 1,3-dibenzyl-2,4-dipentyl), including also the tetrahydroxy compound and the 1,3-dipentyl ether, were synthesised. Their urea groups were substituted with a lipophilic residue to ensure sufficient solubility in cyclohexane. Thus, kinetics for the exchange of the included guest (benzene) against the solvent (cyclohexane) could be followed by 1H NMR spectroscopy. The apparent first order rate constants decrease with increasing size of the ether residues from methyl to benzyl by more than three orders of magnitude. This can be understood by a decreasing flexibi…

Magnetic Resonance SpectroscopyCyclohexaneEtherBiochemistryMedicinal chemistrychemistry.chemical_compoundPhenolsCyclohexanesCalixareneUreaMoleculeOrganic chemistryPhysical and Theoretical ChemistrySolubilityMolecular StructureHydrogen bondOrganic ChemistryBenzeneHydrogen BondingNuclear magnetic resonance spectroscopySolventKineticschemistryCalixarenesDimerizationEthersOrganic & Biomolecular Chemistry
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Conformational Properties of Oxazole-Amino Acids: Effect of the Intramolecular N–H···N Hydrogen Bond

2014

Oxazole ring occurs in numerous natural peptides, but conformational properties of the amino acid residue containing the oxazole ring in place of the C-terminal amide bond are poorly recognized. A series of model compounds constituted by the oxazole-amino acids occurring in nature, that is, oxazole-alanine (L-Ala-Ozl), oxazole-dehydroalanine (ΔAla-Ozl), and oxazole-dehydrobutyrine ((Z)-ΔAbu-Ozl), was investigated using theoretical calculations supported by FTIR and NMR spectra and single-crystal X-ray diffraction. It was found that the main feature of the studied oxazole-amino acids is the stable conformation β2 with the torsion angles φ and ψ of -150°, -10° for L-Ala-Ozl, -180°, 0° for ΔAl…

Magnetic Resonance SpectroscopyDouble bondNitrogenSurface PropertiesStereochemistryMolecular Conformation010402 general chemistry01 natural scienceschemistry.chemical_compoundSpectroscopy Fourier Transform InfraredMaterials ChemistryPeptide bondAmino AcidsPhysical and Theoretical ChemistryOxazolesOxazolechemistry.chemical_classificationAlanine010405 organic chemistryHydrogen bondAminobutyratesHydrogen BondingNuclear magnetic resonance spectroscopyModels Theoretical0104 chemical sciencesSurfaces Coatings and FilmsAmino acidNMR spectra databasechemistryIntramolecular forceSolventsThermodynamicsHydrogenThe Journal of Physical Chemistry B
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