Search results for "Energy-transfer"

showing 10 items of 18 documents

Chlorophyll fluorescence emission spectrum inside a leaf

2008

International audience; Chlorophyll a fluorescence can be used as an early stress indicator. Fluorescence is also connected to photosynthesis so it can be proposed for global monitoring of vegetation status from a satellite platform. Nevertheless, the correct interpretation of fluorescence requires accurate physical models. The spectral shape of the leaf fluorescence free of any re-absorption effect plays a key role in the models and is difficult to measure. We present a vegetation fluorescence emission spectrum free of re-absorption based on a combination of measurements and modelling. The suggested spectrum takes into account the photosystem I and II spectra and their relative contributio…

0106 biological sciencesChlorophyllChlorophyll aSpectral shape analysisI REACTION CENTERSSPINACH THYLAKOID MEMBRANES[SDU.ASTR.EP]Sciences of the Universe [physics]/Astrophysics [astro-ph]/Earth and Planetary Astrophysics [astro-ph.EP]PHOTOSYNTHETIC MEMBRANEPhotosystem I01 natural sciencesSpectral lineHIGHER-PLANTSPROTEIN COMPLEXES03 medical and health scienceschemistry.chemical_compoundmedicineEmission spectrumPhysical and Theoretical ChemistryChlorophyll fluorescenceLIGHT-HARVESTING COMPLEX030304 developmental biologyRemote sensing0303 health sciencesPhotosystem I Protein Complex[SDU.ASTR]Sciences of the Universe [physics]/Astrophysics [astro-ph]Photosystem II Protein Complexfood and beveragesFluorescencePlant LeavesSpectrometry FluorescenceROOM-TEMPERATUREchemistryPHOTOSYSTEM-I[SDU]Sciences of the Universe [physics]Espectroscòpia de fluorescènciaARABIDOPSIS-THALIANAmedicine.symptomVegetation (pathology)ENERGY-TRANSFER010606 plant biology & botany
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Precision and accuracy of single-molecule FRET measurements-a multi-laboratory benchmark study

2018

Single-molecule Forster resonance energy transfer (smFRET) is increasingly being used to determine distances, structures, and dynamics of biomolecules in vitro and in vivo. However, generalized protocols and FRET standards to ensure the reproducibility and accuracy of measurements of FRET efficiencies are currently lacking. Here we report the results of a comparative blind study in which 20 labs determined the FRET efficiencies (E) of several dye-labeled DNA duplexes. Using a unified, straightforward method, we obtained FRET efficiencies with s.d. between +/- 0.02 and +/- 0.05. We suggest experimental and computational procedures for converting FRET efficiencies into accurate distances, and…

0301 basic medicinePHOTON DISTRIBUTIONDYNAMICSAccuracy and precisionTechnologyBiophysicsRESONANCE ENERGY-TRANSFERBiochemistryMedical and Health SciencesArticle03 medical and health sciencesBlind studySingle-molecule biophysicsALTERNATING-LASER EXCITATIONSTRUCTURAL INFORMATIONFluorescence resonance energy transferDEPENDENCEQuantitative assessmentLife ScienceFLUORESCENCEStructure determinationMolecular BiologyQCVLAGBiophysical methodsReproducibilityReproducibility of ResultsCell BiologySingle-molecule FRETDNABiological SciencesPublisher CorrectionQPSPECTROSCOPIC RULER030104 developmental biologyFörster resonance energy transferBiofysicaBenchmark (computing)Photon distributionEPSREFRACTIVE-INDEXLaboratoriesBiological systemBiotechnologyDevelopmental Biology
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DNA structure-specific sensitization of a metalloporphyrin leads to an efficient in vitro quadruplex detection molecular tool

2016

International audience; The search for convenient molecular probes for detecting DNA and RNA quadruplexes in vitro is marked by a rapid pace of progress, spurred on by the multiple roles these higher-order nucleic acid structures play in many genetic dysregulations. Here, we contribute to this search, reporting on a palladated porphyrin named Pd.TEGPy: its efficiency as quadruplex-selective fluorescent dye relies on a structural design that endows it with attractive supramolecular and electronic properties and makes it an efficient turn-on, quadruplex-selective fluorescent stain thanks to a DNA-mediated sensitization mechanism that ensures a high level of specificity.

0301 basic medicineSupramolecular chemistryNanotechnology[ CHIM ] Chemical SciencesCatalysis03 medical and health scienceschemistry.chemical_compoundenergy-transferMaterials Chemistrymedicine[CHIM]Chemical Sciencesheterocyclic compoundsrnaSensitizationComputingMilieux_MISCELLANEOUSvisualizationligandsaggregationselectivityRNAGeneral ChemistryFluorescencePorphyrindye-complexes030104 developmental biologymedicine.anatomical_structurechemistryBiophysicsNucleic acidcellsrecognitionMolecular probeporphyrinDNA
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FRET-based dynamic structural biology: Challenges, perspectives and an appeal for open-science practices.

2021

International audience; Single-molecule FRET (smFRET) has become a mainstream technique for studying biomolecular structural dynamics. The rapid and wide adoption of smFRET experiments by an ever- increasing number of groups has generated significant progress in sample preparation, measurement procedures, data analysis, algorithms and documentation. Several labs that employ smFRET approaches have joined forces to inform the smFRET community about streamlining how to perform experiments and analyze results for obtaining quantitative information on biomolecular structure and dynamics. The recent efforts include blind tests to assess the accuracy and the precision of smFRET experiments among d…

0301 basic medicineconformationOpen scienceComputer scienceStructural Biology and Molecular BiophysicsAMINOACYL-TRANSFER-RNAINTRAMOLECULAR DISTANCE DISTRIBUTIONSReview ArticleRESONANCE ENERGY-TRANSFER01 natural sciencesbiomoleculesFREELY DIFFUSING MOLECULESDocumentationFluorescence Resonance Energy TransferMainstreamstructural biologyBiology (General)General NeuroscienceQRNANO-POSITIONING SYSTEMGeneral MedicinedynamicsINTRINSICALLY DISORDERED PROTEINSSingle Molecule ImagingFLUORESCENCE CORRELATION SPECTROSCOPY[SDV.BBM.BP]Life Sciences [q-bio]/Biochemistry Molecular Biology/BiophysicsMedicinecommunitysingle-moleculeQH301-705.5ScienceAppeal[SDV.BBM.BP] Life Sciences [q-bio]/Biochemistry Molecular Biology/BiophysicsBioengineeringchemical biology010402 general chemistryGeneral Biochemistry Genetics and Molecular Biology03 medical and health sciencesALTERNATING-LASER EXCITATIONBiochemistry and Chemical Biologymolecular biophysicsbiochemistryMolecular BiologyStructure (mathematical logic)General Immunology and MicrobiologySINGLE-MOLECULE FRETTRANSITION PATH TIMESData science0104 chemical sciences030104 developmental biologyFRETPosition paperGeneric health relevanceBiochemistry and Cell BiologyeLife
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Experimental and theoretical studies on thymine photodimerization mediated by oxidatively generated DNA lesions and epigenetic intermediates.

2020

[EN] Interaction of nucleic acids with light is a scientific question of paramount relevance not only in the understanding of life functioning and evolution, but also in the insurgence of diseases such as malignant skin cancer and in the development of biomarkers and novel light-assisted therapeutic tools. This work shows that the UVA portion of sunlight, not absorbed by canonical DNA nucleobases, can be absorbed by 5-formyluracil (ForU) and 5-formylcytosine (ForC), two ubiquitous oxidatively generated lesions and epigenetic intermediates present in living beings in natural conditions. We measure the strong propensity of these molecules to populate triplet excited states able to transfer th…

DNA damagePhotochemistryUltraviolet RaysBasesGeneral Physics and AstronomyPyrimidine dimer010402 general chemistry01 natural sciencesNucleobaseEpigenesis Geneticchemistry.chemical_compoundTriplet energy-transferCytosineQUIMICA ORGANICAMoleculeEpigeneticsPhysical and Theoretical ChemistryUracil010405 organic chemistryDimer formation0104 chemical sciencesThymineDynamicsDamagePhotophysicschemistryBiophysicsNucleic acidSunlightMechanismPhotosensitizationDimerizationOxidation-ReductionDNAThymineDNA DamagePhysical chemistry chemical physics : PCCP
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Collisional Broadening, Line Shifting, and Line Mixing in the Stimulated Raman 2-v2 Q-Branch of CH4

1991

0021-9606; Self-, argon-, and helium-broadening coefficients have been measured for 13 lines in the 2v2 Raman Q branch of CH4 using stimulated inverse Raman spectroscopy. The linewidths clearly show the symmetry-state dependence characteristic of pressure broadening, and inelastic processes in general, involving spherical-top molecules. Pressure-induced line shifts have also been measured for these features in pure methane. The pressure-shift coefficients do not display the symmetry-state dependence found for the linewidths. By applying the Rosenkranz perturbation treatment to a pair of collisionally mixed lines, we have been able to obtain an estimate of individual state-to-state contribut…

DOUBLE-RESONANCETUNABLE DIODE-LASERVIBRATIONAL POLYADSSPECTROSCOPYMETHANE LINESTHEORETICAL-ANALYSISINFRAREDROTATIONAL ENERGY-TRANSFERTETRAHEDRAL MOLECULESPhysics::Atomic PhysicsRATESINELASTICLOW-TEMPERATURES
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Theory for the stationary polariton response in the presence of vibrations

2019

We construct a model describing the response of a hybrid system where the electromagnetic field - in particular, surface plasmon polaritons - couples strongly with electronic excitations of atoms or molecules. Our approach is based on the input-output theory of quantum optics, and in particular it takes into account the thermal and quantum vibrations of the molecules. The latter is described within the $P(E)$ theory analogous to that used in the theory of dynamical Coulomb blockade. As a result, we are able to include the effect of the molecular Stokes shift on the strongly coupled response of the system. Our model then accounts for the asymmetric emission from upper and lower polariton mod…

DYNAMICSQuantum decoherenceFOS: Physical sciences02 engineering and technology01 natural sciencesplasmonicsvärähtelytQuantum mechanics0103 physical sciencesMesoscale and Nanoscale Physics (cond-mat.mes-hall)Polaritonhybrid quantum systemskvanttikemiaMOLECULE010306 general physicskvanttifysiikkaQuantumQuantum opticsPhysicsQuantum PhysicsCondensed Matter - Mesoscale and Nanoscale PhysicsSurface plasmonCoulomb blockade021001 nanoscience & nanotechnologySurface plasmon polaritonSURFACE-PLASMON POLARITONSpintailmiötLight emission0210 nano-technologyQuantum Physics (quant-ph)ENERGY-TRANSFERpolaritonsemissio (fysiikka)
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Collisional Broadening of Rotational Lines in the Stimulated Raman Pentad Q-Branch of CD4

1992

Self- and argon-broadening coefficients are reported for a number of Raman Q-branch transitions in the nu(1) and nu(2) + nu(4) bands of (C-12)D4 at room temperature (296 K). The coefficients display a variation with j and with C exp n (symmetry species A, E, F) that is essentially independent of collision partner and which is similar to the j- and C exp n-dependence found in previous measurements of the IR line-broadening coefficients. The rotationally inelastic collision rates previously measured by Foy et al. (1988) for (C-13)D4 (V4 = 0, 1) in collision with (C-13)D4 or Ar account for only a part of the Raman broadening rate, suggesting possibly significant contributions to the linewidths…

DephasingInelastic collision02 engineering and technologyLORENTZ WIDTH01 natural sciencesLOW-TEMPERATURESSpectral linesymbols.namesakeNuclear magnetic resonance0103 physical sciencesSPECTRAStimulated ramanPhysicsTUNABLE-DIODE-LASERRadiationSPECTROSCOPY010304 chemical physicsINFRARED DOUBLE-RESONANCESpectral bands021001 nanoscience & nanotechnologyAtomic and Molecular Physics and OpticsSymmetry (physics)METHANE LINESCM-1 REGIONsymbolsSHIFT COEFFICIENTSAtomic physics0210 nano-technologyRaman spectroscopyENERGY-TRANSFER
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Near-infrared emissive bacteriochlorin-diketopyrrolopyrrole triads: Synthesis and photophysical properties

2019

International audience; The synthesis of unprecedented energy transfer triads containing a near-infrared (NIR) emissive bacteriochlorin subunit and two diketopyrrolopyrrole (DPP) moieties linked to each other via ethynyl or zero-carbon spacers is presented. Their optical and fluorescence properties were determined in CHCl3 and toluene. These photophysical measurements highlight the ability of DPP scaffold to act as an effective energy donor, which once excited in the range 450-550 nm resulting nearly exclusively NIR emission of hydroporphyrin (ETE > 96%). Since DPP dyes are valuable structurally tunable fluorophores that may be used in the construction of high-performance multicomponent pho…

Energy-transfer triadMaterials science[CHIM.ORGA]Chemical Sciences/Organic chemistryProcess Chemistry and TechnologyGeneral Chemical EngineeringEnergy transferNear-infrared spectroscopyRational design02 engineering and technologyChromophoreFluorophore010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciences7. Clean energyFluorescence0104 chemical sciencesNearinfrared fluorescence HighlightsEffective energyExcited state0210 nano-technologyBacteriochlorinDiketopyrrolopyrrole
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Line mixing in the ν1 and 2ν2 isotropic Raman Q-branch of CO2 perturbed by argon and helium

1999

0021-9606; The shapes of the ν1 and 2ν2 isotropic Raman Q-branch of CO2 perturbed by argon and helium have been measured by Stimulated Raman Spectroscopy (SRS) or coherent anti-Stokes Raman Spectroscopy (CARS) techniques. The data have been successfully analyzed with an energy corrected sudden (ECS) approximation model based on basic rates determined independently. Finally comparison of the present data with time resolved double resonance experiments allows us to discuss the physical origin of the two empirical constants which account for the shift and broadening of the branch due to vibrational effects. (C) 1999 American Institute of Physics. [S0021-9606(99)00344-X].

INFRARED-SPECTRA1000SPECTROSCOPYGASFERMI DYADDOUBLE-RESONANCE EXPERIMENTSROTATIONAL ENERGY-TRANSFERVIBRATIONAL-RELAXATIONPRESSURENU-1/2-NU-2BAND SHAPESBAR
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