Search results for "dimers"

showing 10 items of 38 documents

D-dimer concentrations in acute urticaria in children

2021

Introduction: Urticaria is a clinical entity presenting as wheals, angioedema, or both simul-taneously. Elevated D-dimer levels were reported in the course of chronic spontaneous urticaria. Data regarding D-dimer levels in acute urticaria in children are limited. Objectives: To assess potential associations between duration of glucocorticosteroid (GCS) therapy and D-dimer concentrations in children with acute urticaria. Patients, materials, and methods: Hospital records of 106 children (59 females), aged 5.57 ± 4.91 years, hospitalized in 2014–2018 were analyzed retrospectively. The study group consisted of pediatric patients admitted to the hospital due to severe acute urticaria resistant …

MalePulmonary and Respiratory Medicinemedicine.medical_specialtypediatricsAdolescentUrticariaImmunologyD-dimersglucocorticosteroidsFibrin Fibrinogen Degradation Products03 medical and health sciences0302 clinical medicinechildrenAmbulatory careInternal medicineWhite blood cellD-dimerHumansImmunology and AllergyMedicinePlateletIn patientacute urticariaChildGlucocorticoidsRetrospective StudiesAcute urticariaAngioedemabusiness.industryDisease ManagementInfantGeneral Medicinemedicine.anatomical_structure030228 respiratory systemChild PreschoolAcute DiseaseAntihistaminic drugsFemalemedicine.symptombusinessBiomarkers030215 immunologyAllergologia et Immunopathologia
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Theoretical insight into the intrinsic ultrafast formation of cyclobutane pyrimidine dimers in UV-irradiated DNA: thymine versus cytosine.

2008

The higher formation yields measured in the ultrafast photoinduced formation of cyclobutane thymine dimers (T T) with respect to those of cytosine (C C) are explained, on the basis of ab initio CASPT2 results, by the existence in thymine of more reactive orientations and a less efficient photoreversibility, whereas in cytosine the funnel toward the photolesion becomes competitive with that mediating the internal conversion of the excited-cytosine monomer.

Models MolecularTime FactorsUltraviolet RaysAb initioPyrimidine dimerDNAInternal conversion (chemistry)PhotochemistrySurfaces Coatings and FilmsThymineCyclobutanechemistry.chemical_compoundCytosineMonomerchemistryPyrimidine DimersMaterials ChemistryNucleic Acid ConformationPhysical and Theoretical ChemistryCytosineDNAThymineDNA DamageThe journal of physical chemistry. B
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Specific detection of cyclobutane pyrimidine dimers in phytoplankton DNA by a non-radioactive assay based on T4-endonuclease V digestion.

2001

The effect of artificial and natural UV irradiation on DNA in marine phytoplankton Isochrysis galbana monoculture was investigated. The presence of cyclobutane pyrimidine dimers (CPDs) in unlabelled I. galbana DNA was detected by a non-radiometric alkaline filter elution assay after T4-endonuclease V digestion. The quantity of CPDs was estimated by alkaline agarose gel electrophoresis. Precise determination of the amount of DNA in the presence of I. galbana pigments was achieved by oxazole yellow homodimer (YOYO) dye. T4-endonuclease V-sensitive sites frequency (ESS/kb), measured after exposure to 2-40 kJ m(-2) of artificial UV light, increased in a dose-dependent manner. Twelve hours after…

Environmental EngineeringDNA RepairDNA damageDNA repairUltraviolet RaysPyrimidine dimerIsochrysis galbanachemistry.chemical_compoundPigmentDeoxyribonuclease (Pyrimidine Dimer)Viral ProteinsEnvironmental ChemistryWaste Management and DisposalEndodeoxyribonucleasesbiologyAlkaline filter elution; crude oil; DNA damage; phytoplankton; UV; sunlightbiology.organism_classificationPollutionPetroleumBiochemistrychemistryCell culturePyrimidine Dimersvisual_artAgarose gel electrophoresisPhytoplanktonvisual_art.visual_art_mediumSunlightBiological AssayDNADNA DamageThe Science of the total environment
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Protective effect of trehalose-loaded liposomes against UVB-induced photodamage in human keratinocytes

2014

Trehalose, a naturally occurring non-reducing disaccharide, is known to act as a major protein stabilizer that can reduce ultraviolet B (UVB)-induced corneal damage when topically applied to the eye. However, due to the low skin permeability of trehalose, which makes the development of topical formulations difficult, its use as a skin photoprotective agent has been limited. Previous findings demonstrated that liposomes may significantly improve the intracellular delivery of trehalose. Therefore, the present study aimed to assess the protective effects of trehalose-loaded liposomes against UVB-induced photodamage using the immortalized human keratinocyte cell line, HaCaT. The effects were al…

Ultraviolet radiationKeratinocytesCienciaPyrimidine dimerBiologyPharmacologyPhotoprotective agentGeneral Biochemistry Genetics and Molecular Biologychemistry.chemical_compoundmedicineGeneral Pharmacology Toxicology and PharmaceuticsCiencias médicasLiposomeintegumentary systemGeneral NeurosciencePiel - InvestigaciónTrehaloseArticlesGeneral Medicinemedicine.diseaseTrehaloseProtein carbonylationCyclobutane pyrimidine dimersHaCaTchemistryApoptosisPhotoprotectionImmunology8-hydroxy-2'-deoxyguanosineSkin cancerBiomedical Reports
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Molecular Basis of DNA Photodimerization: Intrinsic Production of Cyclobutane Cytosine Dimers

2008

Based on CASPT2 results, the present contribution establishes for the first time that cytosine photodimer formation (CC) is mediated along the triplet and singlet manifold by a singlet-triplet crossing, (T1/S0)X, and by a conical intersection, (S1/S0)CI, respectively. The former can be accessed in a barrierless way from a great variety of photochemical avenues and exhibits a covalent single bond between the ethene C6-C6' carbon atoms of each monomer. The efficiency of the stepwise triplet mechanism, however, would be modulated by the effectiveness of the intersystem crossing mechanism. The results provide the grounds for the understanding of the potential photogenotoxicity of endogenous and…

Quantitative Biology::BiomoleculesPhotochemistryUltraviolet RaysChemistryDNAGeneral ChemistryConical intersectionPhotochemistryBiochemistryCatalysisCyclobutaneCytosinechemistry.chemical_compoundColloid and Surface ChemistryIntersystem crossingPyrimidine DimersCovalent bondExcited stateNucleic Acid ConformationSingle bondSinglet stateDimerizationCytosineDNA DamageJournal of the American Chemical Society
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Highly efficient construction of infectious viroid-derived clones

2019

[Background] Viroid research generally relies on infectious cDNA clones that consist of dimers of the entire viroid sequence. At present, those dimers are generated by self-ligation of monomeric cDNA, a strategy that presents several disadvantages: (i) low efficiency, (ii) it is a non-oriented reaction requiring tedious screenings and (iii) additional steps are required for cloning into a binary vector for agroinfiltration or for in vitro RNA production.

0106 biological sciences0301 basic medicineAgroinfiltrationIIs enzymesViroidvirusesPlant ScienceComputational biologylcsh:Plant cultureBiology01 natural sciences03 medical and health sciencesAgro-infiltrationComplementary DNAGeneticsLethal allelelcsh:SB1-1110Vector (molecular biology)Dimerslcsh:QH301-705.5CloningViroidMethodologyRNAbiology.organism_classificationRestriction enzyme030104 developmental biologylcsh:Biology (General)010606 plant biology & botanyBiotechnologyCloning
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DNA replication arrest in response to genotoxic stress provokes early activation of stress-activated protein kinases (SAPK/JNK).

2009

Abstract The impact of DNA damage-induced replication blockage for early activation of stress kinases [stress-activated protein kinase (SAPK)/c-Jun N-terminal kinase (JNK)] is largely unknown. Here, we show that induction of dual phosphorylation of SAPK/JNK by the DNA polymerase inhibitor aphidicolin was not ameliorated by additional exposure to ultraviolet (UV) light, indicating that overlapping mechanisms participate in signaling to SAPK/JNK triggered by both agents. UV-induced DNA replication blockage, cyclobutane pyrimidine dimer formation and DNA strand break induction coincided with SAPK/JNK phosphorylation at early (≤ 30 min) but not late (≥ 2 h) time points after exposure. Genotoxin…

AphidicolinDNA ReplicationDNA damageUltraviolet RaysPoly ADP ribose polymeraseCell Linechemistry.chemical_compoundMiceAphidicolinStructural BiologyCricetinaeAnimalsHumansLymphocytesPhosphorylationProtein kinase AMolecular BiologyNucleic Acid Synthesis InhibitorsBRCA2 ProteinMice KnockoutbiologyKinaseCell CycleDNA replicationJNK Mitogen-Activated Protein KinasesFibroblastsMolecular biologyProliferating cell nuclear antigenDNA-Binding ProteinsEnzyme ActivationchemistryPyrimidine Dimersbiology.proteinPhosphorylationApoptosis Regulatory ProteinsDNA DamageJournal of molecular biology
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Intra- and extra-cellular DNA damage by harmine and 9-methyl-harmine

2014

It is known that b-carbolines are able to produce photosensitized damage in cell-free DNA, but there is little information on their effects on cellular DNA. Therefore, we have analyzed the DNA damage produced by harmine and 9-methyl-harmine under UVA irradiation in V79 cells, together with the associated generation of micronuclei and photocytotoxicity. The results indicate that the most frequent photoproducts generated in the cellular DNA are modified purines such as 8-oxo-7,8-dihydroguanine. Only relatively few single-strand breaks were observed. CPDs were absent, although they were generated in cell-free DNA irradiated under the same conditions. The overall extent of DNA damage in the cel…

Guanineb-carbolinesUltraviolet RaysDNA damageBiophysicsFree radical damage to DNACHO CellsMicronucleiBiologyPhototoxicitychemistry.chemical_compoundCricetulusHarmineCyclobutane pyrimidine photodimersCricetinaeAnimalsRadiology Nuclear Medicine and imagingPurine metabolismRadiationRadiological and Ultrasound TechnologyCell growthOtras Ciencias QuímicasCiencias QuímicasDNAHydrogen-Ion ConcentrationHarmineQuímica OrgánicaBiochemistrychemistryMicronucleus testBiophysicsPhotosensitizationPhototoxicityCIENCIAS NATURALES Y EXACTASDNADNA DamageJournal of Photochemistry and Photobiology B: Biology
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On the Intrinsically Low Quantum Yields of Pyrimidine DNA Photodamages: Evaluating the Reactivity of the Corresponding Minimum Energy Crossing Points

2020

The low quantum yield of photoformation of cyclobutane pyrimidine dimers and pyrimidine-pyrimidone (6-4) adducts in DNA bases is usually associated with the presence of more favorable nonreactive decay paths and with the unlikeliness of exciting the system in a favorable conformation. Here, we prove that the ability of the reactive conical intersection to bring the system either back to the absorbing conformation or to the photoproduct must be considered as a fundamental factor in the low quantum yields of the mentioned photodamage. In support of the proposed model, the one order of magnitude difference in the quantum yield of formation of the cyclobutane thymine dimer with respect to the t…

PyrimidineUltraviolet RaysQuantum yieldPyrimidine dimer010402 general chemistryPhotochemistry01 natural sciencesNucleobaseAdductCyclobutanechemistry.chemical_compound0103 physical sciencesComputer SimulationGeneral Materials SciencePhysical and Theoretical Chemistry010304 chemical physicsChemistryDNAConical intersectionPhotochemical Processes0104 chemical sciences3. Good healthThymineEstructura químicaPyrimidine DimersFisicoquímica
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Guest-Induced Folding of the N-Benzyl Substituents in an Ammonium Resorcinarene Chloride and the Formation of a Halogen-Bonded Dimer of Capsules

2016

In methanol, N-benzyl ammonium resorcinarene chloride (Bn-NARCl) crystallizes as a solvate with the benzyl groups oriented in an open flower-like manner parallel to the cation–anion seam. 1,4-Dioxane as guest triggers a “semi-closed” single-molecule capsule with two benzyl “arms” enclosing the guest. The introduction of halogen bond (XB) donor 1,4-diiodoperfluorobutane (1,4-DIOFB) additionally folds the remaining two benzyl arms thus resulting in a fully closed capsule. Two 1,4-DIOFB molecules bridge two such Bn-NARCl capsules, forming a 2:2:2 XB held dimeric assembly of single-molecule capsules. The peculiar behavior was not observed in the bromide analog under similar experimental conditi…

capsulessupramolecular self-assembly processesStereochemistryDimer010402 general chemistry01 natural sciencesChloridechemistry.chemical_compoundBromidemedicineMoleculeGeneral Materials Scienceta116halogen-bonded dimersHalogen bondta114thermodynamically disfavored conformations010405 organic chemistryGeneral ChemistryResorcinareneCondensed Matter Physics0104 chemical sciencesCrystallographychemistryHalogenSingle crystalmedicine.drugCrystal Growth & Design
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