Search results for "Nucleobase"

showing 10 items of 69 documents

Ultrafast dynamics of adenine following XUV ionization

2022

JPhys photonics 4, 034003 (2022). doi:10.1088/2515-7647/ac6ea5 special issue: "Focus on Nanophotonics and Biophotonics for Biomedical and Environmental Applications"

PaperSettore FIS/03ultrafastFocus on Nanophotonics and Biophotonics for Biomedical and Environmental Applicationsdynamicsdissociation530Atomic and Molecular Physics and OpticsSettore FIS/03 - Fisica Della MateriaElectronic Optical and Magnetic MaterialsXUVPhysics::Atomic and Molecular Clustersddc:530Electrical and Electronic EngineeringadeninenucleobaseJOURNAL OF PHYSICS-PHOTONICS
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A modified guanosine phosphoramidite for click functionalization of RNA on the sugar edge

2012

A propargyl containing guanosine phosphoramidite was synthesized and incorporated into siRNA, enabling click-ligation with an azido fluorophore onto the nucleobase sugar edge. Duplex stability was not affected by labeling at this new site, which allowed deconvolution of the effects of label, structure and attachment site on RNAi activity.

PhosphoramiditeFluorophoreGuanosineMolecular StructureCarbohydratesMetals and AlloysGuanosineRNAGeneral ChemistryCombinatorial chemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsNucleobasechemistry.chemical_compoundOrganophosphorus CompoundschemistryDuplex (building)PropargylMaterials ChemistryCeramics and CompositesRNASurface modificationClick ChemistryRNA Small InterferingChemical Communications
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DNA-binding and in vitro cytotoxic activity of platinum(II) complexes of curcumin and caffeine

2019

Abstract Three Pt(II) complexes containing the natural ligands curcumin and caffeine, namely [Pt(curc)(PPh3)2]Cl (1), [PtCl(curc)(DMSO)] (2) (curc = deprotonated curcumin) and trans-[Pt(caffeine)Cl2(DMSO)] (3), were synthesized and fully characterized. The data obtained suggest that, for both 1 and 2, the anion of curcumin is coordinated to the platinum ion via the oxygen atoms of the β-diketonate moiety. Spectroscopic features reveal that in 2 and 3, a DMSO molecule is S-bonded to the metal centre. For 3, all data indicate a square-planar geometry formed by a 9-N bonded caffeine, two trans chloride anions and a DMSO. The three complexes undergo changes in solution upon incubation for 24 h;…

PhotoactivationCurcuminCytotoxicityIntercalation (chemistry)chemistry.chemical_elementCaffeine; Curcumin; Cytotoxicity; DNA interaction; Natural ligands; Photoactivation; Platinum(II) complexAntineoplastic Agents010402 general chemistryLigands01 natural sciencesBiochemistryMedicinal chemistryNucleobaseInorganic Chemistrychemistry.chemical_compoundDrug StabilityCoordination ComplexesCaffeineCell Line TumorMoietyMoleculeAnimalsHumansPlatinumMolecular Structure010405 organic chemistryDNA0104 chemical sciencesDNA interactionchemistryCurcuminPlatinum(II) complexCattleCaffeine Curcumin Cytotoxicity DNA interaction Natural ligands Photoactivation Platinum(II) complexCisplatinDrug Screening Assays AntitumorSelectivityPlatinumNatural ligandsCis–trans isomerism
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Resolving the Benzophenone DNA-Photosensitization Mechanism at QM/MM Level

2015

International audience; Benzophenone, the parent of the diarylketone family, is a versatile compound commonly used as a UV blocker. It may also trigger triplet-based DNA photosensitization. Therefore, benzophenone is involved in DNA photodamage induction. In the absence of experimentally resolved structure, the mechanism of DNA damage production remains elusive. Employing a hybrid quantum mechanics/molecular mechanics approach, here we address the spin transfer mechanism between this drug and proximal thymine, that is, the DNA nucleobase most prone to suffer triplet damages.

Photosensitizing AgentsDNA PhotosensitizationDNA damageChemistryDNAMolecular Dynamics SimulationPhotochemistryMolecular mechanicsQM/MM3. Good healthThymineNucleobaseQM/MM[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryBenzophenoneschemistry.chemical_compoundMolecular dynamicsBenzophenoneEnergy TransferBenzophenoneQuantum TheoryGeneral Materials SciencePhysical and Theoretical ChemistryDNA
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Orientation, recognition, and photoreaction of nucleolipids in model membranes

1990

Amphiphiles with nucleobases and nucleosides as headgroups have been synthesized. Their surface behavior was investigated in monolayers at the air/water interface. The double chain nucleolipids form stable monolayers with nearly identical surface pressure-area diagrams, whereas the spreading behavior of the mono chain amphiphiles is dominated by the various nucleobase-headgroups. When measuring the interactions between nucleolipid monolayers and nucleobases (monomeric and polymeric ones), specific base-base effects could be observed: the complementary nucleobases solubilized in the subphase expand the monolayer more than the non-complementary ones. Photodimerization reactions of thymine-amp…

Polymers and PlasticsStereochemistrytechnology industry and agricultureSynthetic membraneNucleobaseDouble chainCrystallographychemistry.chemical_compoundColloid and Surface ChemistryMonomerMembranechemistrySolubilizationMonolayerAmphiphileMaterials ChemistryPhysical and Theoretical ChemistryColloid & Polymer Science
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A bioinspired metal–organic approach to cross-linked functional 3D nanofibrous hydro- and aero-gels with effective mixture separation of nucleobases …

2020

The direct reaction between Cu(CH3COO)2 and uracil-1-acetic acid in water gives rise to the formation of a hydrogel consisting of entangled nanometric ribbons of a crystalline antiferromagnetic 1D Cu(ii) coordination polymer (CP) decorated with biocompatible uracil nucleobases. This hydrogel is the precursor for the preparation of a meso/macroporous ultralight aerogel that shows a remarkable Young's modulus. As a proof-of-concept of the molecular recognition capability of the terminal uracil moieties anchored at Cu(ii) CP chains, this material has been tested as the selective stationary phase for the separation of nucleobase derivatives in HPLC columns.

PolymersCoordination polymerNanofibersHydrogelsAerogelUracil02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesHigh-performance liquid chromatography0104 chemical sciencesNucleobaseMetalchemistry.chemical_compoundMolecular recognitionchemistryChemical engineeringMetalsvisual_artvisual_art.visual_art_mediumGeneral Materials ScienceDirect reaction0210 nano-technologyCopperNanoscale
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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
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Hydrogen bonding patterns of 7,9-dimethylguanine and its transplatinum(II) complexes

2002

Methylation at the N7 position is one of the most frequently naturally occurring modifications of guanosine. This alteration drastically changes the hydrogen bonding and acid–base properties of the guanine nucleobase. Here we show on the example of the model nucleobase 7,9-dimethylguanine that due to blockage of N7 of the purine ring, new hydrogen bonding patterns occur on the minor groove binding face of this nucleobase involving the ring nitrogen N3 and the exocyclic amino group N2H2. The free 7,9-dimethylguaninium ion and several transplatinum(II) complexes of the this ligand are presented and discussed. Methylation at N7 drastically changes the acid–base and hydrogen bonding properties …

Purine10120 Department of ChemistryTransplatinumLigandStereochemistryGuanineHydrogen bond1604 Inorganic ChemistryInorganic chemistryGuanosineRing (chemistry)Nucleobase complexeNucleobaseIonHydrogen bondsInorganic Chemistrychemistry.chemical_compoundchemistryModified nucleobaseSettore CHIM/03 - Chimica Generale E Inorganica540 ChemistryMaterials ChemistryPhysical and Theoretical Chemistry1606 Physical and Theoretical Chemistry2505 Materials Chemistry
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On the Use of Metal Purine Derivatives (M=Ir, Rh) for the Selective Labeling of Nucleosides and Nucleotides

2014

The reactions of neutral or cationic IrIII and RhIII derivatives of phenyl purine nucleobases with unsymmetrical alkynes produce new metallacycles in a predictable manner, which allows for the incorporation of either photoactive (anthracene or pyrene) or electroactive (ferrocene) labels in the nucleotide or nucleoside moiety. The reported methodology (metalation of the purine derivative and subsequent marker insertion) could be used for the postfunctionalization and unambiguous labeling of oligonucleotides.

PurineMetalationIridiumCatalysisNucleobasechemistry.chemical_compoundOrganometallic CompoundsOrganic chemistryMoietyRhodiumNucleotideNuclear Magnetic Resonance BiomolecularPurine NucleotidesAnthraceneschemistry.chemical_classificationPyrenesMolecular StructureOrganic ChemistryCationic polymerizationPurine NucleosidesGeneral ChemistryCombinatorial chemistryFerrocenechemistryAlkynesNucleosideChemistry - A European Journal
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Surface-Enhanced Raman Study of the Interactions between Tripodal Cationic Polyamines and Polynucleotides

2011

Raman and surface-enhanced Raman spectra of new DNA/RNA-binding compounds consisting of three imidazole (Im) and three pyridine (Py) rings connected by tripodal polyaminomethylene linkages were obtained by the near-infrared excitation at 1064 nm. Study of interactions of Im and Py polyamines with single-stranded RNA polynucleotides (poly A, poly G, poly C, poly U), double-stranded DNA polynucleotides (poly dAdT-poly dAdT, poly dGdC-poly dGdC) and calf thymus DNA (ct-DNA) by surface-enhanced Raman spectroscopy (SERS) reveals unambiguous enhancement of the Raman scattering from the small molecules as well as appearance of new bands in spectra associated mainly with nucleobases. The SERS exper…

PyrimidinePyridinesStereochemistryGuaninePolynucleotidesSpectrum Analysis RamanBiochemistryAnalytical ChemistryNucleobasechemistry.chemical_compoundsymbols.namesakePolyaminesElectrochemistryAnimalsEnvironmental ChemistryImidazoleSpectroscopyImidazolesAromaticityDNAsurface-enhanced Raman spectroscopy ; polyamines ; polynucleotides ; DNAchemistryPolynucleotidesymbolsRNACattleRaman spectroscopyDNA
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