Search results for "Tandem"

showing 10 items of 560 documents

Pressurized liquid extraction combined with capillary electrophoresis–mass spectrometry as an improved methodology for the determination of sulfonami…

2007

A new analytical method, based on capillary electrophoresis and tandem mass spectrometry (CE-MS2), is proposed and validated for the identification and simultaneous quantification of 12 sulfonamides (SAs) in pork meat. The studied SAs include sulfathiazole, sulfadiazine, sulfamethoxypyridazine, sulfaguanidine, sulfanilamide, sulfadimethoxyne, sulfapyridine, sulfachloropyridazine, sulfisoxazole, sulfasalazine, sulfabenzamide and sulfadimidine. Different parameters (i.e. separation buffer, sheath liquid, electrospray conditions) were optimized to obtain an adequate CE separation and high MS sensitivity. MS2 experiments using an ion trap as analyzer, operating in the selected reaction monitori…

Quality ControlMeatSwineFood ContaminationComplex MixturesMass spectrometryTandem mass spectrometrySensitivity and SpecificityBiochemistryCapillary electrophoresis–mass spectrometryAnalytical ChemistryCapillary electrophoresisTandem Mass SpectrometryPressuremedicineAnimalsSample preparationSulfonamidesChromatographyChemistrySulfadimidineOrganic ChemistrySelected reaction monitoringSulfabenzamideElectrophoresis CapillaryWaterGeneral MedicineCalibrationFood AnalysisChromatography Liquidmedicine.drugJournal of Chromatography A
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Plasma pharmacokinetics and tissue distribution study of cajaninstilbene acid in rats by liquid chromatography with tandem mass spectrometry

2010

Cajaninstilbene acid (CSA; 3-hydroxy-4-prenyl-5-methoxystilbene-2-carboxylic acid) is a major active constituent of pigeonpea leaves, has been proven to be effective in clinical treatment of diabetes, hepatitis, measles and dysentery. A rapid and sensitive liquid chromatography tandem mass spectrometry (LC-MS/MS) method was developed and validated for the determination of CSA in rat plasma and various tissues (brain, heart, lung, liver, spleen, small intestine and kidney) of rat for the first time. Rat plasma and tissue distribution pre-treated by protein precipitation with acetoacetate was analyzed using LC-MS/MS with an electrospray ionization (ESI) interface, and isoliquiritigenin was us…

Quality ControlTime FactorsMetabolic Clearance RateFormic acidElectrospray ionizationClinical BiochemistryCarboxylic AcidsPharmaceutical ScienceTandem mass spectrometrySensitivity and SpecificityHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundCajanusDrug StabilityPharmacokineticsTandem Mass SpectrometryLiquid chromatography–mass spectrometryFreezingStilbenesDrug DiscoveryAnimalsProtein precipitationTissue DistributionSpectroscopyChromatographyMolecular StructureTemperatureReproducibility of ResultsHalf-lifeRats Inbred StrainsReference StandardsSalicylatesRatschemistryArea Under CurveCalibrationFemaleChromatography LiquidHalf-LifeJournal of Pharmaceutical and Biomedical Analysis
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Are analysts doing method validation in liquid chromatography?

2014

International audience; Method validation is being applied in the reported analytical methods for decades. Even before this protocol was defined, authors already somehow validated their methods without full awareness. They wished to assure the quality of their work. Validation is an applied approach to verify that a method is suitable and rugged enough to function as a quality control tool in different locations and times. The performance parameters and statistical protocols followed throughout a validation study vary with the source of guidelines. Before single laboratory validation, an analytical method should be fully developed and optimized. The purpose of the validation is to confirm p…

Quality ControlValidation studyDIODE-ARRAY DETECTIONMethod validationmedia_common.quotation_subjectLiquid chromatographyValidation Studies as TopicGuidelinesBiochemistryField (computer science)Analytical Chemistry[CHIM.ANAL]Chemical Sciences/Analytical chemistrySIMPLE HPLC METHODHumansQuality (business)HUMAN PLASMATANDEM MASS-SPECTROMETRYRAT PLASMAFunction (engineering)SurveyRP-LC METHODmedia_commonProtocol (science)AnalystsChromatographyPoint (typography)ChemistryData CollectionOrganic ChemistryGeneral MedicineEvaluated validation parametersMethod developmentFully developedSOLID-PHASE EXTRACTIONESI-MS/MS METHODPHARMACEUTICAL DOSAGE FORMChromatography LiquidTHIN-LAYER-CHROMATOGRAPHY
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Unexpected metal-free synthesis of trifluoromethyl arenes via tandem coupling of dicyanoalkenes and conjugated fluorinated sulfinyl imines

2021

A novel strategy for the synthesis of policyclic trifluoromethyl arenes has been devised. It involves a DBU-promoted tandem cycloaromatization reaction of dicyanoalkenes and fluorinated conjugated sulfinyl imines. This unprecedented transformation is a metal-free and air-tolerant process that takes place from readily available starting materials under mild reaction conditions.

Reaction conditionsTrifluoromethylTandem010405 organic chemistryMetals and AlloysGeneral ChemistryConjugated system010402 general chemistry01 natural sciencesCombinatorial chemistryCatalysis0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundMetal freechemistryMaterials ChemistryCeramics and CompositesChemical Communications
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RepeatsDB in 2021: improved data and extended classification for protein tandem repeat structures

2020

The RepeatsDB database (URL: https://repeatsdb.org/) provides annotations and classification for protein tandem repeat structures from the Protein Data Bank (PDB). Protein tandem repeats are ubiquitous in all branches of the tree of life. The accumulation of solved repeat structures provides new possibilities for classification and detection, but also increasing the need for annotation. Here we present RepeatsDB 3.0, which addresses these challenges and presents an extended classification scheme. The major conceptual change compared to the previous version is the hierarchical classification combining top levels based solely on structural similarity (Class > Topology > Fold) with two new lev…

Repetitive Sequences Amino AcidAcademicSubjects/SCI00010BiologíaStatistics as TopicProtein Data Bank (RCSB PDB)Computational biologyBiologyRepetitive SequencesGene Ontology; HEK293 Cells; HeLa Cells; Humans; Proteins; Reproducibility of Results; Statistics as Topic; User-Computer Interface; Databases Protein; Repetitive Sequences Amino Acid; Tandem Repeat SequencesDatabases03 medical and health sciencesAnnotationUser-Computer InterfaceProtein structureSimilarity (network science)Tandem repeatGeneticsDatabase IssueHumansDatabases ProteinCiencias Exactasdatabase030304 developmental biology0303 health sciencesHierarchy (mathematics)Protein030302 biochemistry & molecular biologyProteinsReproducibility of Resultscomputer.file_formatProtein Data BankClass (biology)proteinsAmino AcidComputingMethodologies_PATTERNRECOGNITIONGene OntologyHEK293 CellsclassificationTandem Repeat Sequencesprotein tandem repeat structures[INFO.INFO-BI]Computer Science [cs]/Bioinformatics [q-bio.QM]computerHeLa CellsNucleic Acids Research
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REP2: A Web Server to Detect Common Tandem Repeats in Protein Sequences

2020

Ensembles of tandem repeats (TRs) in protein sequences expand rapidly to form domains well suited for interactions with proteins. For this reason, they are relatively frequent. Some TRs have known structures and therefore it is advantageous to predict their presence in a protein sequence. However, since most TRs diverge quickly, their detection by classical sequence comparison algorithms is not very accurate. Previously, we developed a method and a web server that used curated profiles and thresholds for the detection of 11 common TRs. Here we present a new web server (REP2) that allows the analysis of TRs in both individual and aligned sequences. We provide currently precomputed analyses f…

Repetitive Sequences Amino AcidWeb serverProteomeComputer scienceComputational biologycomputer.software_genreEvolution Molecular03 medical and health sciences0302 clinical medicineTandem repeatStructural BiologySequence comparisonHumansAmino Acid SequenceMolecular BiologyConserved Sequence030304 developmental biologySequence (medicine)Comparative genomicsInternet0303 health sciencesMultiple sequence alignmentBacteriaProteinsTandem Repeat SequencesProteomeUniProtSequence Alignmentcomputer030217 neurology & neurosurgeryJournal of Molecular Biology
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Tumor-Associated MUC1 Tandem-Repeat Glycopeptide Microarrays to Evaluate Serum- and Monoclonal-Antibody Specificity

2009

Repetitive Sequences Amino Acidmedicine.drug_classMolecular Sequence DataMonoclonal antibodyCatalysisMiceTandem repeatAntibody SpecificityNeoplasmsmedicineAnimalsAmino Acid SequencePeptide sequenceMUC1biologyMicroarray analysis techniquesChemistryImmune SeraMucin-1GlycopeptidesAntibodies MonoclonalGeneral MedicineGeneral ChemistryMicroarray AnalysisMolecular biologyGlycopeptideBiochemistrybiology.proteinAntibodyDNA microarrayAngewandte Chemie International Edition
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2014

In the resurging field of RNA modifications, quantification is a bottleneck blocking many exciting avenues. With currently over 150 known nucleoside alterations, detection and quantification methods must encompass multiple modifications for a comprehensive profile. LC–MS/MS approaches offer a perspective for comprehensive parallel quantification of all the various modifications found in total RNA of a given organism. By feeding 13C-glucose as sole carbon source, we have generated a stable isotope-labeled internal standard (SIL-IS) for bacterial RNA, which facilitates relative comparison of all modifications. While conventional SIL-IS approaches require the chemical synthesis of single modif…

Response factorAbsolute quantificationRNABiologyTandem mass spectrometryPseudouridineIsotopomerschemistry.chemical_compoundchemistryBiochemistryGeneticsCalibrationBiological systemNucleosideNucleic Acids Research
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Metabolomic Analysis of the Effect of Postnatal Hypoxia on the Retina in a Newly Born Piglet Model

2013

The availability of reliable biomarkers of brain injury secondary to birth asphyxia could substantially improve clinical grading, therapeutic intervention strategies, and prognosis. In this study, changes in the metabolome of retinal tissue caused by profound hypoxia in an established neonatal piglet model were investigated using an ultra performance liquid chromatography - quadrupole time of flight mass spectrometry (UPLC-QTOFMS) untargeted metabolomic approach, which included Partial Least Squares - Discriminant Analysis (PLSDA) multivariate data analysis. The initial identification of a set of discriminant metabolites from UPLC-QTOFMS data was confirmed by target UPLC-MS/MS and allowed t…

ResuscitationSwinelcsh:MedicineBrain damageBioinformaticsBiochemistryPediatricsRetinachemistry.chemical_compoundMetabolomicsDiagnostic MedicinePregnancyTandem Mass SpectrometryPathologyMetabolomemedicineAnimalsMetabolomicsEye ProteinsHypoxialcsh:ScienceBiologyLiquid ChromatographyAsphyxiaChromatographyMultidisciplinarybusiness.industrylcsh:RObstetrics and GynecologyRetinalHypoxia (medical)Pregnancy ComplicationsChemistryMetabolismAnimals NewbornchemistrySmall MoleculesMedicineBiomarker (medicine)lcsh:QMetabolic PathwaysNeonatologymedicine.symptombusinessBiomarkersResearch ArticleGeneral PathologyChromatography LiquidPLoS ONE
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Metabolomic changes in the rat retina after optic nerve crush.

2013

Purpose To identify metabolic pathways and metabolites affected by optic nerve crush that can act as predictors of the disease or therapeutic targets. Methods The left optic nerve of adult rats was intraorbitally crushed and retinas were dissected 24 hours or 14 days after the lesion (n = 10 per group). Metabolic profiling analysis was carried out by Metabolon, Inc. A total of 195 metabolites were unambiguously detected. Data were normalized and the regulated metabolites were identified after comparing the different conditions. Metabolite concentration changes were analyzed using single and multivariate statistical analysis to detect discriminatory metabolites. Functional clustering and met…

Retinal Ganglion CellsNerve CrushMetaboliteProtein Array AnalysisApoptosisPharmacologymedicine.disease_causeGas Chromatography-Mass SpectrometryRetinaLesionRats Sprague-Dawleychemistry.chemical_compoundMetabolomicsTandem Mass SpectrometrymedicineAnimalsMetabolomicsAmino AcidsChemistryLipid metabolismAxotomyOptic NerveLipid MetabolismAxonsRatsMetabolic pathwayOxidative StressOptic nerveCarbohydrate MetabolismFemaleMetabolonmedicine.symptomOxidative stressChromatography LiquidSignal TransductionInvestigative ophthalmologyvisual science
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