Search results for "Biomolecule"

showing 10 items of 666 documents

Investigation of protein folding by coarse-grained molecular dynamics with the UNRES force field.

2010

Coarse-grained molecular dynamics simulations offer a dramatic extension of the time-scale of simulations compared to all-atom approaches. In this article, we describe the use of the physics-based united-residue (UNRES) force field, developed in our laboratory, in protein-structure simulations. We demonstrate that this force field offers about a 4000-times extension of the simulation time scale; this feature arises both from averaging out the fast-moving degrees of freedom and reduction of the cost of energy and force calculations compared to all-atom approaches with explicit solvent. With massively parallel computers, microsecond folding simulation times of proteins containing about 1000 r…

Protein FoldingStaphylococcus aureusRotationMolecular Dynamics SimulationKinetic energyForce field (chemistry)Protein Structure SecondaryArticleMolecular dynamicsMiceProtein structureBacterial ProteinsComputational chemistryAnimalsStatistical physicsPhysical and Theoretical ChemistryMassively parallelQuantitative Biology::BiomoleculesPrincipal Component AnalysisModels StatisticalChemistryProteinsMicrosecondKineticsBundleSolventsThermodynamicsProtein foldingTranscriptional Elongation FactorsCarrier ProteinsAlgorithmsProtein BindingThe journal of physical chemistry. A
researchProduct

Recent Advances in Affinity MOF-Based Sorbents with Sample Preparation Purposes

2020

This review summarizes the recent advances concerning metal–organic frameworks (MOFs) modified with several biomolecules (e.g., amino acids, nucleobases, proteins, antibodies, aptamers, etc.) as ligands to prepare affinity-based sorbents for application in the sample preparation field. The preparation and incorporation strategies of these MOF-based affinity materials were described. Additionally, the different types of ligands that can be employed for the synthesis of these biocomposites and their application as sorbents for the selective extraction of molecules and clean-up of complex real samples is reported. The most important features of the developed biocomposites will be discussed thr…

ProteomicsPolymersAptamerCarbohydratesaptamersPharmaceutical ScienceBiocompatible MaterialsNanotechnologyReviewLigandsbiomoleculesAnalytical ChemistryPhysical Phenomenalcsh:QD241-441metal–organic frameworkslcsh:Organic chemistryBiomimeticsDrug DiscoveryHumansantibodiessolid-phase extractionSample preparationPhysical and Theoretical Chemistrysample treatmentMetal-Organic Frameworkschemistry.chemical_classificationamino acidsBiomoleculeSolid Phase ExtractionOrganic ChemistryfungiProteinsmolecular imprinted polymersnucleobasesChemistrychemistryChemistry (miscellaneous)Microscopy Electron ScanningMolecular MedicineMetal-organic frameworkAdsorptionProtein BindingMolecules
researchProduct

The ins and outs of proton complexation

2009

Proton complexation differs from simple protonation by the fact that the coordinated hydrogen atom is bound intramolecularly to more than one donor atom. This is usually achieved by covalent bonding supplemented by hydrogen bonding. In a few cases, however, the complexed proton is hydrogen-bound to all donor atoms, which gives rise to single well (SWHB) and low barrier (LBHB) hydrogen bonds. This tutorial review highlights a full range of proton complexes formed with chelating and "proton-sponge"-type ligands, cryptand-like macropolycycles, and molecules of topological relevance, such as rotaxanes and catenanes. The concept of proton complexation can explain how the smallest cation possible…

ProtonStereochemistryLow-barrier hydrogen bondreviewProtonation010402 general chemistry01 natural sciencescovalent bonding[ CHIM.ORGA ] Chemical Sciences/Organic chemistryMoleculePhysics::Atomic PhysicsPhysics::Chemical Physicsproton complexationNuclear ExperimentComputingMilieux_MISCELLANEOUSQuantitative Biology::Biomolecules[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistryChemistryHydrogen bondGeneral ChemistryHydrogen atomhydrogen bonding3. Good health0104 chemical sciencesCrystallographyCovalent bondIntramolecular forceChemical Society Reviews
researchProduct

Charge-Neutral Constant pH Molecular Dynamics Simulations Using a Parsimonious Proton Buffer

2016

In constant pH molecular dynamics simulations, the protonation states of titratable sites can respond to changes of the pH and of their electrostatic environment. Consequently, the number of protons bound to the biomolecule, and therefore the overall charge of the system, fluctuates during the simulation. To avoid artifacts associated with a non-neutral simulation system, we introduce an approach to maintain neutrality of the simulation box in constant pH molecular dynamics simulations, while maintaining an accurate description of all protonation fluctuations. Specifically, we introduce a proton buffer that, like a buffer in experiment, can exchange protons with the biomolecule enabling its…

ProtonprotonationAnalytical chemistryProtonationBuffersMolecular Dynamics Simulation010402 general chemistry01 natural sciencesBuffer (optical fiber)Molecular dynamics0103 physical sciencesPhysical and Theoretical ChemistryNuclear Experimentta116chemistry.chemical_classificationQuantitative Biology::Biomolecules010304 chemical physicspHQuantitative Biology::Molecular NetworksBiomoleculeProteinsCharge (physics)molecular dynamics simulationselectrostatic environmentHydrogen-Ion Concentration0104 chemical sciencesComputer Science ApplicationschemistryChemical physicsThermodynamicsTitrationbufferProtonsConstant (mathematics)Journal of Chemical Theory and Computation
researchProduct

Hardy-Orlicz Spaces of conformal densities

2014

We define and prove characterizations of Hardy-Orlicz spaces of conformal densities.

Pure mathematicsQuantitative Biology::BiomoleculesMathematics::Functional AnalysisHardy spacesMathematics::Complex Variables010102 general mathematicsta111Mathematics::Classical Analysis and ODEsConformal mapHardy spaceMathematics::Spectral Theoryconformal densities01 natural sciencesHardy-Orliczsymbols.namesakeMathematics - Classical Analysis and ODEs0103 physical sciencesClassical Analysis and ODEs (math.CA)FOS: Mathematicssymbols010307 mathematical physicsGeometry and Topology0101 mathematics30C35 (Primary) 30H10 (Secondary)MathematicsConformal Geometry and Dynamics
researchProduct

Biosensors for the determination of SARS-CoV-2 virus and diagnosis of COVID-19 infection

2022

Monitoring and tracking infection is required in order to reduce the spread of the coronavirus disease 2019 (COVID-19), induced by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). To achieve this goal, the development and deployment of quick, accurate, and sensitive diagnostic methods are necessary. The determination of the SARS-CoV-2 virus is performed by biosensing devices, which vary according to detection methods and the biomarkers which are inducing/providing an analytical signal. RNA hybridisation, antigen-antibody affinity interaction, and a variety of other biological reactions are commonly used to generate analytical signals that can be precisely detected using electro…

QH301-705.5immune complexSARS-CoV-2 virusBiosensing TechniquesReviewCatalysisInorganic Chemistryelectrochemical immunosensorsCOVID-19 TestingHumansSerologic TestsPhysical and Theoretical ChemistryBiology (General)Molecular BiologyQD1-999SpectroscopySARS-CoV-2bioelectrochemistryOrganic ChemistryCOVID-19General MedicineRNA analysisbiosensorsimmobilisation of biomoleculesNanostructuresComputer Science ApplicationsChemistryMolecular Diagnostic Techniquesmolecularly imprinted polymers (MIPs)antigen-antibody interactionCOVID-19 ; SARS-CoV-2 virus ; biosensors ; electrochemical immunosensors ; bioelectrochemistry ; RNA analysis ; antigen-antibody interaction ; immune complex ; immobilisation of biomolecules ; molecularly imprinted polymers (MIPs)
researchProduct

The FRET-based structural dynamics challenge -- community contributions to consistent and open science practices

2020

Single-molecule F\"{o}rster resonance energy transfer (smFRET) has become a mainstream technique for probing biomolecular structural dynamics. The rapid and wide adoption of the technique by an ever-increasing number of groups has generated many improvements and variations in the technique itself, in methods for sample preparation and characterization, in analysis of the data from such experiments, and in analysis codes and algorithms. Recently, several labs that employ smFRET have joined forces to try to bring the smFRET community together in adopting a consensus on how to perform experiments and analyze results for achieving quantitative structural information. These recent efforts includ…

Quantitative Biology - BiomoleculesBiological Physics (physics.bio-ph)FOS: Biological sciencesFOS: Physical sciencesBiomolecules (q-bio.BM)Physics - Biological Physics
researchProduct

4-Benzoyl-3,4-dihydro-2 H -1,4-benzoxazine-2-carbonitrile: refinement using a multipolar atom model

2009

The structural model for the title compound, C(16)H(12)N(2)O(2), was refined using a multipolar atom model transferred from an experimental electron-density database. The refinement showed some improvements of crystallographic statistical indices when compared with a conventional spherical neutral-atom refinement. The title compound adopts a half-chair conformation. The amide N atom lies almost in the plane defined by the three neighbouring C atoms. In the crystal structure, molecules are linked by weak intermolecular C-H...O and C-H...pi hydrogen bonds.

Quantitative Biology::Biomolecules010405 organic chemistryChemistryHydrogen bondStatistical indexIntermolecular forceGeneral MedicineCrystal structure010402 general chemistry01 natural sciencesGeneral Biochemistry Genetics and Molecular Biology3. Good health0104 chemical scienceschemistry.chemical_compoundCrystallographyAmideAtom[CHIM.CRIS]Chemical Sciences/CristallographyMoleculePhysics::Atomic PhysicsComputingMilieux_MISCELLANEOUSAtom model
researchProduct

2015

AbstractLight absorption can trigger biologically relevant protein conformational changes. The light-induced structural rearrangement at the level of a photoexcited chromophore is known to occur in the femtosecond timescale and is expected to propagate through the protein as a quake-like intramolecular motion. Here we report direct experimental evidence of such ‘proteinquake’ observed in myoglobin through femtosecond X-ray solution scattering measurements performed at the Linac Coherent Light Source X-ray free-electron laser. An ultrafast increase of myoglobin radius of gyration occurs within 1 picosecond and is followed by a delayed protein expansion. As the system approaches equilibrium i…

Quantitative Biology::Biomolecules0303 health sciencesMultidisciplinaryMaterials sciencePhotodissociationFree-electron laserGeneral Physics and Astronomy02 engineering and technologyGeneral ChemistryChromophore021001 nanoscience & nanotechnologyMolecular physicsGeneral Biochemistry Genetics and Molecular Biology03 medical and health scienceschemistry.chemical_compoundMyoglobinchemistryPicosecondFemtosecondRadius of gyrationsense organsPhysics::Chemical Physics0210 nano-technologyUltrashort pulse030304 developmental biologyNature Communications
researchProduct

Vibrational dephasing of νs(OH) in 2,6-dichloro-4-nitrophenol

1988

Abstract A detailed analysis of the infrared bandshape of ν s (OH) in intramolecularly hydrogen-bonded 2,6-dichloro-4-nitrophenol in a series of solvents is presented. A distinct dependence of the bandshape and relaxation parameters on the polarity of solvent molecules has been found. The band shifts to lower wavenumbers, broadens and becomes more Gaussian with increasing solvent polarity; correspondingly, the correlation function decays faster and the correlation time decreases. The results are compared with those of previously studied systems. Factors determing the bandshape are discussed.

Quantitative Biology::Biomolecules2 6 dichloro 4 nitrophenolInfraredChemistryPolarity (physics)DephasingOrganic ChemistryRelaxation (NMR)Analytical ChemistryInorganic ChemistrySolventCorrelation functionComputational chemistryPhysical chemistryMoleculePhysics::Chemical PhysicsSpectroscopyJournal of Molecular Structure
researchProduct