Search results for "nucleotides"

showing 10 items of 297 documents

An isocratic high-pressure liquid chromatographic purification method for radioactively labeled deoxyribonucleoside triphosphates.

1976

Abstract A method is described for the rapid purification of radioactively labeled deoxyribonucleoside tri­phosphates from their spontaneously emerging hydrolysis products deoxyribonucleoside diphosphate, deoxyribonucleoside monophosphate, and deoxyribonucleoside. The separations which are finished within 3 min or less are carried out on a 0.1X5 cm column filled with LiChrosorb-NH2 , using isocratic elution with 0.025 м potassium phosphate, pH 6 .8 , in a high-pressure liquid chromatograph at room temperature and a flow rate of 30 ml · h-1(flow velocity 63.7 cm·min-1).

Deoxyribonucleosidechemistry.chemical_compoundHydrolysisIsocratic elutionChromatographychemistryPotassium phosphateHigh pressureDeoxyribonucleotidesPurification methodsGeneral Biochemistry Genetics and Molecular BiologyChromatography High Pressure LiquidZeitschrift fur Naturforschung. Section C, Biosciences
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Insights into how nucleotide supplements enhance the peroxidase-mimicking DNAzyme activity of the G-quadruplex/hemin system

2012

Since the initial discovery of the catalytic capability of short DNA fragments, this peculiar enzyme-like property (termed DNAzyme) has continued to garner much interest in the scientific community because of the virtually unlimited applications in developing new molecular devices. Alongside the exponential rise in the number of DNAzyme applications in the last past years, the search for convenient ways to improve its overall efficiency has only started to emerge. Credence has been lent to this strategy by the recent demonstration that the quadruplex-based DNAzyme proficiency can be enhanced by ATP supplements. Herein, we have made a further leap along this path, trying first of all to deci…

DeoxyribozymeNanotechnologyBiology010402 general chemistryG-quadruplex01 natural sciencesCatalysischemistry.chemical_compoundAdenosine TriphosphateGeneticsNucleotideCatalytic efficiencyComputingMilieux_MISCELLANEOUSchemistry.chemical_classificationSupplementary data010405 organic chemistryNucleotides[CHIM.CATA]Chemical Sciences/CatalysisDNADNA Catalytic0104 chemical sciences[SDV.BBM.BP]Life Sciences [q-bio]/Biochemistry Molecular Biology/BiophysicsG-QuadruplexesCatalytic cyclechemistryBiochemistryPeroxidasesSynthetic Biology and ChemistryHeminOverall efficiencyHeminNucleic Acids Research
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Dip Pen Lithography of oligonucleotides on flexible substrates for point-of-care malaria disease testing

2015

The first step for prevention and treatment of diseases is the accurate diagnosis. However, proper diagnostic technologies are not available in developing countries due to the lack of reliable electrical power, refrigeration and trained personnel. For this reason, there is an urgent need of low cost, rapid assays not requiring any external support. By coupling such technologies to communication infrastructures, healthcare in areas without access to medical personnel would be possible. “Paper” like substrates are ideal for fabricating such devices since they are cheap, easy to degradate after use and compatible with most of existing printing technologies [1]. We had previously shown the poss…

Dip Pen Lithography oligonucleotides flexible substrates malaria
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Pharmacokinetics of oligodeoxynucleotides encapsulated in liposomes: effect of lipid composition and preparation method

2000

1. The effect of the method employed to prepare liposomes and their lipid composition were evaluated in terms of the encapsulation efficiency and pharmacokinetic features of two oligodeoxynucleotides of a 21 mer: the normal (N-Odn) and the phosphorothioate (S-Odn) oligodeoxynucleotide. 2. Liposomes were prepared by the classical method of multilamellar vesicles (MV) and by the dehydration-rehydration method (DR). Two lipid mixtures were used to prepare liposomes--the predominant lipid being phosphatidylcholine (PC) and sphingomyelin (SM) respectively. 3. The DR method for liposome preparation provided the highest encapsulation efficiency, regardless of liposome lipid composition and the typ…

Drug CompoundingHealth Toxicology and MutagenesisLipid compositionMultilamellar vesiclesToxicologyBiochemistryPreparation methodMicechemistry.chemical_compoundPharmacokineticsPhosphatidylcholineAnimalsPharmacologyPlasma clearanceLiposomeChromatographyChemistryhemic and immune systemsGeneral MedicineThionucleotidesrespiratory systemLipidsOligodeoxyribonucleotidesBiochemistryInjections IntravenousLiposomesSphingomyelinXenobiotica
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A novel approach for analysis of oligonucleotide-cisplatin interactions by continuous elution gel electrophoresis coupled to isotope dilution inducti…

2008

In this work we present a novel approach for in vitro studies of cisplatin interactions with 8-mer oligonucleotides. The approach is based on the recently developed coupling of continuous elution gel electrophoresis (GE) to an inductively coupled plasma-sector field mass spectrometer (ICP-SFMS) with the aim of monitoring the interaction process between this cytostatic drug and the nucleotides. In contrast to existing methods, the electrophoretic separation conditions used here allow both the determination of the reaction kinetics in more detail as well as the observation of dominant intermediates. Two different nucleotides sequences have been investigated for comparison purposes, one contai…

ElectrophoresisChromatographyProtein mass spectrometryElutionChemistryClinical BiochemistryAnalytical chemistryOligonucleotidesAntineoplastic AgentsMass spectrometryBiochemistryCapillary electrophoresis–mass spectrometrySample preparation in mass spectrometryAnalytical ChemistrySurface-enhanced laser desorption/ionizationMatrix-assisted laser desorption/ionizationKineticsSpectrometry Mass Matrix-Assisted Laser Desorption-IonizationCisplatinInductively coupled plasma mass spectrometryElectrophoresis
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Function of RAR? and RAR?2 at the initiation of retinoid signaling is essential for avian embryo survival and for distinct events in cardiac morphoge…

2003

Avian embryogenesis requires retinoid receptor activation by the vitamin A active form, retinoic acid (RA), during neurulation. We conducted loss-of-function analysis in quail embryos by nutritional deprivation of RA and by blocking generation of retinoid receptors. Here we identify a distinct role for RARα2 in cardiac inflow tract morphogenesis and for RARγ in cardiac left/right orientation and looping morphogenesis. Blocking normal embryos with antisense oligonucleotides to RARα2 or RXRα diminishes GATA-4 transcripts, while blocking RARγ or RXRα diminishes nodal and Pitx2 transcripts; the expression of these genes in the heart forming region resembles that of the vitamin A-deficient embry…

Embryo NonmammalianTime Factorsanimal structuresCell SurvivalReceptors Retinoic Acidmedicine.drug_classMorphogenesisRetinoic acidRetinoid receptorCoturnixBiologyRetinoidschemistry.chemical_compoundmedicineAnimalsRNA MessengerRetinoidIn Situ HybridizationHomeodomain ProteinsGeneticsRetinoid X receptor alphaPITX2MyocardiumRetinoic Acid Receptor alphaGene Expression Regulation DevelopmentalOligonucleotides AntisenseGATA4 Transcription FactorCell biologyDNA-Binding ProteinsPhenotypeRetinoid X ReceptorschemistrySignal transductionNODALSignal TransductionTranscription FactorsDevelopmental BiologyDevelopmental Dynamics
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Endoribonuclease IV. A poly(A)-specific ribonuclease from chick oviduct. 1. Purification of the enzyme.

1976

A new endoribonuclease, termed endoribonuclease IV, has been described. This enzyme has been isolated from chick oviducts and purified 15 000-fold in a 25% yield nearly to homogeneity. The nuclease, which specifically degrades poly(A), forms oligonucleotides of an average chain length of 10. These (A)-10 fragments are terminated by 3'-hydroxyl and 5'-phosphate groups. The enzyme has a pH optimum at 8.7, requires Mn2+ or Mg2+ as a cofactor, and has a molecular weight of about 45 000.

EndoribonucleaseOviductsBiologyBiochemistryCofactorStructure-Activity RelationshipRibonucleasesAnimalsMagnesiumchemistry.chemical_classificationNucleaseManganeseOligoribonucleotidesOligonucleotideEndoribonuclease IVEndonucleasesMolecular biologyEnzyme ActivationMolecular WeightKineticsEnzymeBiochemistrychemistryYield (chemistry)biology.proteinOviductFemalePoly AChickensEuropean journal of biochemistry
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Analysis of the TK enzyme complex induced by HSV types 1 and 2 by means of isoelectric focusing and polyacrylamide gel electrophoresis.

1982

Recently we have described that the Herpes simplex virus (HSV)-induced thymidine kinase (TK) induces AMP- and ADP-dThd-5'-phosphotransferase activities. We now demonstrate the heterogeneity of the described activities in isoelectric focusing experiments and polyacrylamide gel electrophoresis. A TK--mutant of HSV type 1 fails to induce these activities. The activities of the type 1 enzyme complex was neutralized by an anti-HSV-serum. The TK-enzyme complex expressed in LTK--cells transformed to a TK+-phenotype by sheared HSV-1 DNA was compared with the wild type TK complex in isoelectric focusing experiments. Additionally we demonstrate that the HSV type 1 enzyme complex has thymidylate kinas…

Enzyme complexvirusesThymidylate kinase activityBiologymedicine.disease_causeThymidine KinaseFeedbackchemistry.chemical_compoundViral ProteinsVirologymedicineSimplexvirusThymine NucleotidesPolyacrylamide gel electrophoresisIsoelectric focusingWild typeGeneral MedicineVirologyMolecular biologyHerpes simplex virusBiochemistrychemistryThymidine kinaseElectrophoresis Polyacrylamide GelIsoelectric FocusingDNAArchives of virology
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General Principles for the Detection of Modified Nucleotides in RNA by Specific Reagents.

2021

Epitranscriptomics heavily rely on chemical reagents for the detection, quantification, and localization of modified nucleotides in transcriptomes. Recent years have seen a surge in mapping methods that use innovative and rediscovered organic chemistry in high throughput approaches. While this has brought about a leap of progress in this young field, it has also become clear that the different chemistries feature variegated specificity and selectivity. The associated error rates, e.g., in terms of false positives and false negatives, are in large part inherent to the chemistry employed. This means that even assuming technically perfect execution, the interpretation of mapping results issuin…

False positives and false negativesBiomedical Engineering[SDV.BBM.BM] Life Sciences [q-bio]/Biochemistry Molecular Biology/Molecular biology01 natural sciencesGeneral Biochemistry Genetics and Molecular Biology570 Life sciencesBiomaterialsReaction rate03 medical and health sciences[SDV.BBM.GTP]Life Sciences [q-bio]/Biochemistry Molecular Biology/Genomics [q-bio.GN]Reactivity (chemistry)NucleotideRNA Processing Post-TranscriptionalComputingMilieux_MISCELLANEOUS030304 developmental biologychemistry.chemical_classification0303 health sciences010405 organic chemistryNucleotidesRNA[SDV.BBM.BM]Life Sciences [q-bio]/Biochemistry Molecular Biology/Molecular biology0104 chemical scienceschemistryReagent[SDV.BBM.GTP] Life Sciences [q-bio]/Biochemistry Molecular Biology/Genomics [q-bio.GN]RNAIndicators and ReagentsRibonucleosidesBiological systemSelectivity570 BiowissenschaftenAdvanced biology
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Molecular recognition of nucleotides in water by scorpiand-type receptors based on nucleobase discrimination.

2014

Abstract: The detection of nucleotides is of crucial impor-tance because they are the basic building blocks of nucleicacids. Scorpiand-based polyamine receptors functionalizedwith pyridine or anthracene units are able to form stablecomplexes with nucleotides in water, based on coulombic,p–p stacking, and hydrogen-bonding interactions. This be-havior has been rationalized by means of an explorationwith NMR spectroscopy and DFT calculations. Binding con-stants were determined by potentiometry. Fluorescencespectroscopy studies have revealed the potential of these re-ceptors as sensors to effectively and selectively distinguishguanosine-5’-triphosphate (GTP) from adenosine-5’-triphos-phate (ATP…

GTP'StereochemistryStackingSupramolecular chemistrysensorsCatalysissupramolecular chemistryNucleobaseMolecular recognitionAdenosine TriphosphateMoleculeNucleotidescorpiandsNuclear Magnetic Resonance Biomolecularchemistry.chemical_classificationMolecular StructureNucleotidesOrganic ChemistryWaterHydrogen BondingGeneral ChemistryNuclear magnetic resonance spectroscopyModels TheoreticalSpectrometry Fluorescencechemistrymolecular recognitionGuanosine TriphosphateChemistry (Weinheim an der Bergstrasse, Germany)
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