Search results for "Structural Biology."

showing 10 items of 822 documents

The conformational properties ofα,β-dehydroamino acids with aC-terminal ester group

2011

α,β-Dehydroamino acid esters occur in nature. To investigate their conformational properties, a systematic theoretical analysis was performed on the model molecules Ac-ΔXaa-OMe [ΔXaa = ΔAla, (E)-ΔAbu, (Z)-ΔAbu, ΔVal] at the B3LYP/6-311+ + G(d,p) level in the gas phase as well as in chloroform and water solutions with the self-consistent reaction field-polarisable continuum model method. The Fourier transform IR spectra in CCl(4) and CHCl(3) have been analysed as well as the analogous solid state conformations drawn from The Cambridge Structural Database. The ΔAla residue has a considerable tendency to adopt planar conformations C5 (ϕ, ψ ≈ - 180°, 180°) and β2 (ϕ, ψ ≈ - 180°, 0°), regardless…

Pharmacologychemistry.chemical_classificationDepsipeptideChloroformStereochemistryOrganic ChemistryInfrared spectroscopyGeneral MedicineBiochemistryAmino acidchemistry.chemical_compoundsymbols.namesakeFourier transformchemistryStructural BiologyDrug DiscoverysymbolsSide chainMolecular MedicinePolarMoleculeMolecular BiologyJournal of Peptide Science
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Conformational investigation of α,β-dehydropeptides. XVI. β-turn tendency in Ac-Pro-ΔXaa-NHMe: crystallographic and theoretical studies

2006

The crystal structures of two diastereomeric alpha,beta-dehydrobutyrine peptides Ac-Pro-(Z)-DeltaAbu-NHMe (I) and Ac-Pro-(E)-DeltaAbu-NHMe (II) have been determined. Both dehydropeptides adopt betaI-turn conformation characterized by the pairs of (phi(i+1), psi(i+1)) and (phi(i+2), psi(i+2)) angles as -66, -19, -97, 11 degrees for I and -59, -27, -119, 29 degrees for II. In each peptide, the betaI turn is stabilized by (i + 3) --> i intramolecular hydrogen bonds with N...O distance of 3.12 A for I and 2.93 A for II. These structures have been compared to the crystal structures of homologous peptides Ac-Pro-DeltaVal-NHMe and Ac-Pro-DeltaAla-NHMe. Theoretical analyses by DFT/B3LYP/6-31 + G** …

Pharmacologychemistry.chemical_classificationHydrogen bondStereochemistryOrganic ChemistrySubstituentPeptideGeneral MedicineCrystal structureBiochemistryPeptide ConformationTurn (biochemistry)Crystallographychemistry.chemical_compoundchemistryStructural BiologyIntramolecular forceDrug DiscoveryMolecular MedicineMolecular BiologyConformational isomerismJournal of Peptide Science
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Novel cleavable cell-penetrating peptide-drug conjugates: synthesis and characterization

2014

We report the first drug conjugate with a negatively charged amphipathic cell-penetrating peptide. Furthermore, we compare two different doxorubicin cell-penetrating peptide conjugates, which are both unique in their properties, due to their net charge at physiological pH, namely the positively charged octaarginine and the negatively charged proline-rich amphipathic peptide. These conjugates were prepared exploiting a novel heterobifunctional crosslinker to join the N-terminal cysteine residue of the peptides with the aliphatic ketone of doxorubicin. This small linker contains an activated thiol as well as aminooxy functionality, capable of generating a stable oxime bond with the C-13 carbo…

Pharmacologychemistry.chemical_classificationStereochemistryOrganic ChemistryPeptideGeneral MedicineGlutathioneBiochemistryResidue (chemistry)chemistry.chemical_compoundchemistryStructural BiologyDrug DiscoveryDrug deliveryCell-penetrating peptideMolecular MedicineMolecular BiologyLinkerConjugateCysteineJournal of Peptide Science
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The effect of β-methylation on the conformation of α, β-dehydrophenylalanine: a DFT study

2009

Dehydroamino acids are non-coded amino acids that offer unique conformational properties. Dehydrophenylalanine (ΔPhe) is most commonly used to modify bioactive peptides to constrain the topography of the phenyl ring in the side chain, which commonly serves as a pharmacophore. The Ramachandran maps (in the gas phase and in CHCl3 mimicking environments) of ΔPhe analogues with methyl groups at the β position of the side chain as well as at the C-terminal amide were calculated using the B3LYP/6-31 + G** method. Unexpectedly, β-methylation alone results in an increase of conformational freedom of the affected ΔPhe residue. However, further modification by introducing an additional methyl group a…

Pharmacologychemistry.chemical_classificationSteric effectsStereochemistryOrganic ChemistryGeneral MedicineDihedral angleBiochemistryAmino acidchemistry.chemical_compoundchemistryStructural BiologyAmideDrug DiscoverySide chainMolecular MedicineMolecular BiologyConformational isomerismRamachandran plotMethyl groupJournal of Peptide Science
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Time scale of protein aggregation dictated by liquid-liquid demixing

2003

The growing impact of protein aggregation pathologies, together with the current high need for extensive information on protein structures are focusing much interest on the physics underlying the nucleation and growth of protein aggregates and crystals. Sickle Cell Hemoglobin (HbS), a point-mutant form of normal human Hemoglobin (HbA), is the first recognized and best-studied case of pathologically aggregating protein. Here we reanalyze kinetic data on nucleation of deoxy-HbS aggregates by referring them to the (concentration-dependent) temperature Ts characterizing the occurrence of the phase transition of liquid-liquid demixing (LLD) of the solution. In this way, and by appropriate scalin…

Phase transitionSpinodalProtein ConformationChemistryHemoglobin SickleTemperatureNucleationProtein aggregationBiochemistryChemical kineticsKineticsCrystallographyProtein structureSolubilityStructural BiologyChemical physicsHumansProtein crystallizationMolecular BiologyScalingProteins: Structure, Function, and Genetics
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Regulation of Phenotypic Switching and Heterogeneity in Photorhabdus luminescens Cell Populations.

2019

Phenotypic heterogeneity in bacterial cell populations allows genetically identical organisms to different behavior under similar environmental conditions. The Gram-negative bacterium Photorhabdus luminescens is an excellent organism to study phenotypic heterogeneity since their life cycle involves a symbiotic interaction with soil nematodes as well as a pathogenic association with insect larvae. Phenotypic heterogeneity is highly distinct in P. luminescens. The bacteria exist in two phenotypic forms that differ in various morphologic and phenotypic traits and are therefore distinguished as primary (1°) and secondary (2°) cells. The 1 cells are bioluminescent, pigmented, produce several sec…

Phenotypic switchingBacterial Physiological Phenomena03 medical and health sciences0302 clinical medicineSymbiosisBacterial ProteinsStructural BiologyPhotorhabdus luminescensSymbiosisMolecular BiologyOrganism030304 developmental biologyGenetics0303 health sciencesLife Cycle StagesbiologyGenetic heterogeneityPigmentationQuorum SensingPhenotypic traitGene Expression Regulation Bacterialbiology.organism_classificationPhenotypeNematodePhenotypeBiological Variation PopulationPhotorhabdus030217 neurology & neurosurgeryJournal of molecular biology
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Modulation of neuronal phospholipase D activity under depolarizing conditions

1999

Neuronal phospholipase D (PLD) activity was hypothesized to be involved in vesicle trafficking and endocytosis and, possibly, transmitter release. We here report that prolonged depolarization of rat hippocampal slices by potassium chloride (KCl) or 4-aminopyridine inhibited PLD activity. Similarly, PLD activity in rat cortical synaptosomes was significantly inhibited by depolarizing agents including veratridine and ouabain. Inhibition of calcium/calmodulin kinase II (CaMKII) which positively modulates synaptosomal PLD activity [Sarri et al. (1998) FEBS Lett. 440, 287-290] by KN-62 caused a further reduction of PLD activity in depolarized synaptosomes. Depolarization-induced inhibition of PL…

Phosphatidylinositol 45-DiphosphateTime FactorsBiophysicschemistry.chemical_elementCalciumHippocampusBiochemistryOuabainMembrane PotentialsPotassium Chloridechemistry.chemical_compoundStructural BiologyCa2+/calmodulin-dependent protein kinaseSynaptosomeElectrochemistryPhospholipase DGeneticsmedicineAnimalsPhospholipase D activityEnzyme InhibitorsRats WistarMolecular BiologyProtein Kinase CProtein Synthesis InhibitorsSynaptosomePhospholipase DCalcium/calmodulin-dependent protein kinase IINeomycinDepolarizationPhosphatidylinositol-45-bisphosphateCell BiologyRatsCell biologyenzymes and coenzymes (carbohydrates)chemistryCalcium-Calmodulin-Dependent Protein KinasesDepolarizationlipids (amino acids peptides and proteins)VeratridineSynaptosomesmedicine.drugFEBS Letters
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PRK1 phosphorylates MARCKS at the PKC sites: serine 152, serine 156 and serine 163

1996

AbstractThe 80kDa Myristolated Alanine-Rich C-Kinase Substrate (MARCKS) in a major in vivo substrate of protein kinase C (PKC). Here we report that MARCKS is a major substrate for the lipid-activated PKC-related kinase (PRK1) in cell extracts. Furthermore, PRK1 is shown to phosphorylate MARCKS on the same sites as PKC in vitro. Thus, control of MARCKS phosphorylation on these previously identified ‘PKC’ sites may be regulated under certain circumstances by PRK as well as PKC mediated signalling pathways. The implications for MARCKS as a marker of PKC activation and as a point of signal convergence are discussed.

PhosphopeptidesMARCKSPRKRecombinant Fusion ProteinsMolecular Sequence DataBiophysicsKidneyBiochemistryCell-free systemCell LineSerineStructural BiologyProtein kinase CGeneticsAnimalsAmino Acid SequenceBinding siteMARCKSPKCPhosphorylationMyristoylated Alanine-Rich C Kinase SubstrateMolecular BiologyProtein kinase CGlutathione TransferaseBinding SitesCell-Free SystemKinaseChemistryIntracellular Signaling Peptides and ProteinsMembrane ProteinsProteinsCell BiologyHaplorhiniPeptide FragmentsBiochemistryPhosphorylationElectrophoresis Polyacrylamide GelSignal transductionSequence AnalysisSignal TransductionFEBS Letters
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Biocomposite PBAT/lignin blown films with enhanced photo-stability.

2022

Lignin can be obtained as a byproduct during cellulose-rich pulp fibers production and it is habitually treated as waste or intended for low-value destinations. However, due to UV absorption and mechanical properties, lignin can contribute to the fabrication of biodegradable blown films with superior performances. In this study, it was established the suitability of lignin for manufacturing biocomposite PBAT blown films with higher stiffness and photo-oxidation resistance. The effect of the filler concentration on the melt rheological behavior in non-isothermal elongational flow was investigated. The results allowed us to choose the correct filler concentration for producing films through a…

Photo-oxidative resistanceSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialiStructural BiologyElastic ModulusPBATGeneral MedicineCelluloseMolecular BiologyBiochemistryLigninBiocomposite blown filmInternational journal of biological macromolecules
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Unveiling the timescale of the R-T transition in human hemoglobin.

2010

Time-resolved wide-angle X-ray scattering, a recently developed technique allowing to probe global structural changes of proteins in solution, was used to investigate the kinetics of R-T quaternary transition in human hemoglobin and to systematically compare it to that obtained with time-resolved optical spectroscopy under nearly identical experimental conditions. Our data reveal that the main structural rearrangement associated with the R-T transition takes place approximately 2 mus after the photolysis of hemoglobin at room temperature and neutral pH. This finding suggests that the 20-mus step observed with time-resolved optical spectroscopy corresponds to a small and localized structural…

PhotochemistryProtein ConformationKineticsMethemoglobinHemoglobinsStructural BiologyHumansScattering RadiationSpectroscopyMolecular BiologyallosteryScatteringChemistryProtein dynamicsSpectrum AnalysisPhotodissociationhemoglobinHydrogen-Ion ConcentrationSettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)CrystallographyKineticsStructural changeChemical physicshemoglobin; allostery; protein dynamicsprotein dynamicssense organsHemoglobinJournal of molecular biology
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