Search results for "Matrix-Assisted Laser Desorption-Ionization"

showing 10 items of 131 documents

Saliva electrophoretic protein profiles in infants: changes with age and impact of teeth eruption and diet transition.

2011

International audience; Objective : The objective of this study was to describe the changes in salivary protein profiles in infants between the ages of 3 and 6 months, and to evaluate the impact of teeth eruption and introduction of solid foods on such profiles. Design : 73 infants were followed longitudinally at 3 and 6 months of age. Their whole saliva proteins were separated by SDS–PAGE electrophoresis and semi-quantified by image analysis. Amylase activity was also measured on a sub-sample of the population (n=42 infants). Bands which abundance was significantly different between the two ages according to paired comparisons were identified by mass spectrometry techniques. Results : Out …

MaleSalivaTooth eruptionPhysiologyTooth Eruption0302 clinical medicineTandem Mass Spectrometry[SDV.IDA]Life Sciences [q-bio]/Food engineeringAmylaseLongitudinal StudiesProspective Studies0303 health scienceseducation.field_of_studybiologyChemistryinfantsGeneral MedicineInfant FormulaBiochemistryAmylasesSalivary CystatinsElectrophoresis Polyacrylamide GelFemaleInfant FoodIntroduction of solid foodamylaseSpectrometry Mass Electrospray IonizationproteomePopulationslivaWeaning03 medical and health sciencesWeaningHumans[SPI.GPROC]Engineering Sciences [physics]/Chemical and Process EngineeringCystatin AProtease InhibitorsCystatin BSalivary Proteins and PeptideseducationGeneral DentistrycystatinSerum Albumin030304 developmental biologyMilk HumanBeta-2 microglobulinSalivary CystatinsAlbuminInfant030206 dentistryCell BiologyDietSecretory ComponentOtorhinolaryngologySpectrometry Mass Matrix-Assisted Laser Desorption-Ionizationbiology.proteinproteinbeta 2-Microglobulinteeth eruptionChromatography LiquidFollow-Up StudiesArchives of oral biology
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Proteomic Analysis of Protein Components in Periodontal Ligament Fibroblasts

2005

BACKGROUND: Characterization of periodontal ligament (PDL) fibroblast proteome is an important tool for understanding PDL physiology and regulation and for identifying disease-related protein markers. PDL fibroblast protein expression has been studied using immunological methods, although limited to previously identified proteins for which specific antibodies are available. METHODS: We applied proteomic analysis coupled with mass spectrometry and database knowledge to human PDL fibroblasts. RESULTS: We detected 900 spots and identified 117 protein spots originating in 74 different genes. In addition to scaffold cytoskeletal proteins, e.g., actin, tubulin, and vimentin, we identified protein…

MaleSpectrometry Mass Electrospray IonizationAdolescentProteomeFluorescent Antibody TechniqueVimentinProteomicsPeptide Mappingperidontal ligamentproteomicsstomatognathic systemmedicineMembrane activityHumansPeriodontal fiberElectrophoresis Gel Two-DimensionalSettore BIO/06 - Anatomia Comparata E CitologiaChildDatabases ProteinFibroblastCytoskeletonCells CulturedActinbiologyperiodontal ligamentProteinsFibroblastsCell biologyCytoskeletal Proteinsmedicine.anatomical_structureSpectrometry Mass Matrix-Assisted Laser Desorption-IonizationProteomebiology.proteinPeriodonticsFibroblastFemaleIsoelectric Focusing
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A New Nuclear Function of the Entamoeba histolytica Glycolytic Enzyme Enolase: The Metabolic Regulation of Cytosine-5 Methyltransferase 2 (Dnmt2) Act…

2009

Cytosine-5 methyltransferases of the Dnmt2 family function as DNA and tRNA methyltransferases. Insight into the role and biological significance of Dnmt2 is greatly hampered by a lack of knowledge about its protein interactions. In this report, we address the subject of protein interaction by identifying enolase through a yeast two-hybrid screen as a Dnmt2-binding protein. Enolase, which is known to catalyze the conversion of 2-phosphoglycerate (2-PG) to phosphoenolpyruvate (PEP), was shown to have both a cytoplasmatic and a nuclear localization in the parasite Entamoeba histolytica. We discovered that enolase acts as a Dnmt2 inhibitor. This unexpected inhibitory activity was antagonized by…

MethyltransferaseQH301-705.5ImmunologyEnolaseProtozoan ProteinsPolymerase Chain ReactionMicrobiologyEntamoeba histolyticaTwo-Hybrid System TechniquesGenetics and Genomics/EpigeneticsVirologyGeneticsImmunoprecipitationDNA (Cytosine-5-)-MethyltransferasesMicrobiology/ParasitologyBiology (General)Molecular BiologyMolecular Biology/DNA MethylationCell Nucleuschemistry.chemical_classificationbiologyEntamoeba histolyticaInfectious Diseases/Protozoal InfectionsMethylationRC581-607biology.organism_classificationTRNA MethyltransferasesEnolase 2EnzymechemistryBiochemistryPhosphopyruvate HydrataseSpectrometry Mass Matrix-Assisted Laser Desorption-IonizationParasitologyImmunologic diseases. AllergyNuclear localization sequenceResearch ArticlePLoS Pathogens
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Identification of cryptic Candida species by MALDI-TOF mass spectrometry, not all MALDI-TOF systems are the same: focus on the C. parapsilosis specie…

2016

Data about the performance of MALDI-TOF mass spectrometry against cryptic Candida species are limited. According to our findings within the C. parapsilosis species complex, microbiologists should be aware that the choice of the instrument is critical for accurate species identification due to the risk of misidentification in the clinical setting.

Microbiological Techniques0301 basic medicineMicrobiology (medical)Species complex030106 microbiologyComputational biologyBiologyMass spectrometrySensitivity and SpecificityMicrobiology[ SDV.EE.SANT ] Life Sciences [q-bio]/Ecology environment/Health03 medical and health sciencesC. parapsilosisHumans[SDV.EE.SANT] Life Sciences [q-bio]/Ecology environment/HealthSpecies identificationComputingMilieux_MISCELLANEOUSCandida[SDV.EE.SANT]Life Sciences [q-bio]/Ecology environment/HealthCandidiasisGeneral MedicineMALDI-TOF Mass Spectrometry3. Good healthInfectious DiseasesSpectrometry Mass Matrix-Assisted Laser Desorption-IonizationIdentification (biology)
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Optimization of the preanalytical steps of matrix-assisted laser desorption ionization-time of flight mass spectrometry identification provides a fle…

2012

ABSTRACT We report here that modifications of the preanalytical steps of matrix-assisted laser desorption ionization–time of flight mass spectrometry (MALDI-TOF MS) identification of yeasts, with regard to the original protocol provided by the manufacturers, appear to be efficient for the reliable routine identification of clinical yeast isolates in medical laboratories. Indeed, when one colony was sampled instead of five and the protein extraction protocol was modified, the performance of MALDI-TOF MS was superior to that of the API ID 32C method (discrepancies were confirmed by using molecular identification), allowing the correct identification of 94% of the 335 clinical isolates prospec…

Microbiology (medical)Microbiological TechniquesTime Factorsmedical laboratories[SDV]Life Sciences [q-bio]clinical yeast isolatesMatrix assisted laser desorption ionization time of flightMycologyMass spectrometrySpecimen Handlingflight mass spectrometry03 medical and health sciencesYeastsHumansionization-time030304 developmental biologyMolecular identification0303 health sciencesChromatography030306 microbiologyChemistryYeastCulture MediaIdentification (information)Mycosesmatrix-assisted laserSpectrometry Mass Matrix-Assisted Laser Desorption-Ionization[SDE]Environmental SciencesidentificationJournal of clinical microbiology
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Mixed-model of ANOVA for measurement reproducibility in proteomics

2009

This work is a statistical analysis of reproducibility of a MALDI-TOF mass spectrometry experiment. Its aim is to evaluate measurement variability and compare peak intensities from two types of MALDI-TOF platforms. We compared and commented on the abilities of Principal Component Analysis and mixed-model analysis of variance to evaluate the biological variability and the technical variability of peak intensities in different patients. The properties and hypotheses of both methods are summarized and applied to spectra from plasma of patients with Hodgkin lymphoma. Principal Component Analysis checks rapidly the balance between the two variabilities; however, a mixed-model analysis of varianc…

Mixed modelProteomicsQuality Control030213 general clinical medicine[SDV.OT]Life Sciences [q-bio]/Other [q-bio.OT]ProteomeBiophysicsAnalytical chemistryProteomicsBiochemistryMass Spectrometry03 medical and health sciences0302 clinical medicineStatisticsHumans030304 developmental biologyMathematicsMeasurement variabilityMeasurement reproducibility0303 health sciencesReproducibilityAnalysis of VariancePrincipal Component AnalysisComputersReproducibility of ResultsVariance (accounting)Blood ProteinsHodgkin DiseaseSpectrometry Mass Matrix-Assisted Laser Desorption-IonizationPrincipal component analysisAnalysis of varianceAdsorptionPeptidesSoftware
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Structure of an outer surface lipoprotein BBA64 from the Lyme disease agent Borrelia burgdorferi which is critical to ensure infection after a tick b…

2013

Lyme disease is a tick-borne infection caused by the transmission of Borrelia burgdorferi from infected Ixodes ticks to a mammalian host during the blood meal. Previous studies have shown that the expression of B. burgdorferi surface-localized lipoproteins, which include BBA64, is up-regulated during the process of tick feeding. Although the exact function of BBA64 is not known, this lipoprotein is critical for the transmission of the spirochete from the tick salivary glands to the mammalian organism after a tick bite. Since the mechanism of development of the disease and the functions of the surface lipoproteins associated with borrel­iosis are still poorly understood, the crystal structur…

Models MolecularAntigens BacterialLyme DiseasebiologyIxodesTransmission (medicine)General MedicineTickbacterial infections and mycosesbiology.organism_classificationmedicine.diseaseMicrobiologyPathogenesisLyme diseaseX-Ray DiffractionStructural BiologyBorrelia burgdorferiSpectrometry Mass Matrix-Assisted Laser Desorption-IonizationmedicineAnimalsIxodesBorrelia burgdorferiFunction (biology)LipoproteinActa crystallographica. Section D, Biological crystallography
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Structure and Function of CutC Choline Lyase from Human Microbiota Bacterium Klebsiella pneumoniae.

2015

CutC choline trimethylamine-lyase is an anaerobic bacterial glycyl radical enzyme (GRE) that cleaves choline to produce trimethylamine (TMA) and acetaldehyde. In humans, TMA is produced exclusively by the intestinal microbiota, and its metabolite, trimethylamine oxide, has been associated with a higher risk of cardiovascular diseases. Therefore, information about the three-dimensional structures of TMA-producing enzymes is important for microbiota-targeted drug discovery. We have cloned, expressed, and purified the CutC GRE and the activating enzyme CutD from Klebsiella pneumoniae, a representative of the human microbiota. We have determined the first crystal structures of both the choline-…

Models MolecularKlebsiella pneumoniaeMetaboliteTrimethylamineLyasesmacromolecular substancesBiologydigestive systemBiochemistryMicrobiologyCholinechemistry.chemical_compoundBacterial ProteinsCatalytic DomainCholineChymotrypsinHumansMolecular Biologychemistry.chemical_classificationChymotrypsinMicrobiotaCell Biologybiology.organism_classificationLyaseEnzyme structureProtein Structure TertiaryKlebsiella pneumoniaeEnzymechemistryBiochemistrySpectrometry Mass Matrix-Assisted Laser Desorption-IonizationProtein Structure and Foldingbiology.proteinChromatography GelElectrophoresis Polyacrylamide GelProtein MultimerizationThe Journal of biological chemistry
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Hydrogen-bond-mediated self-assembly of 26-membered diaza tetraester crowns of 3,5-disubstituted 1 h -pyrazole. Dimerization study in the solid state…

2011

By using an improved synthetic method reported earlier, the cyclic stannoxanes obtained from RN-diethanolamine (R = Me, Bu) and dibutyltin oxide have been reacted with 1H-pyrazole-3,5-dicarbonyl dichloride to afford 26-membered diaza tetraester crowns (1, R = Me; 3, R = Bu) and 39-membered triaza hexaester crowns (2, R = Me; 4, R = Bu). The new structures were identified from their analytical and spectroscopic (1H and 13C NMR, FAB-MS, and/or ESI-MS) data. Both diaza tetraester crowns (1 and 3), containing two 1H-pyrazole units, self-assemble into dimeric species through the formation of four hydrogen bonds involving the two NH pyrazole groups and the two tertiary amine groups of both crowns…

Models MolecularMagnetic Resonance SpectroscopyMolecular modelTertiary amineSolid-statePyrazoleCrystallography X-RayMedicinal chemistrychemistry.chemical_compoundOrganotin CompoundsAminesDibutyltin oxideHydrogen bondOrganic ChemistryEstersHydrogen BondingCarbon-13 NMRDeuteriumCrown CompoundsSolutionschemistryCyclizationEthanolaminesMolecular ProbesSpectrometry Mass Matrix-Assisted Laser Desorption-IonizationPyrazolesChloroformSelf-assemblyDimerization
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Mapping the fluorophilicity of a hydrophobic pocket: synthesis and biological evaluation of tricyclic thrombin inhibitors directing fluorinated alkyl…

2006

In the completion of our fluorine scan of tricyclic inhibitors to map the fluorophilicity/fluorophobicity of the thrombin active site, a series of 11 new ligands featuring alkyl, alkenyl, and fluoroalkyl groups was prepared to explore fluorine effects on binding into the hydrophobic proximal (P) pocket, lined by Tyr 60A and Trp 60D, His 57, and Leu 99. The synthesis of the tricyclic scaffolds was based on the 1,3-dipolar cycloaddition of azomethine ylides, derived from L-proline and 4-bromobenzaldehyde, with N-(4-fluorobenzyl)maleimide. Introduction of alkyl, alkenyl, and partially fluorinated alkyl residues was achieved upon substitution of a sulfonyl group by mixed Mg/Zn organometallics f…

Models MolecularMagnetic Resonance SpectroscopySpectrophotometry InfraredStereochemistrySubstituentCrystallography X-RayBiochemistryAntithrombinschemistry.chemical_compoundDrug DiscoveryNon-covalent interactionsGeneral Pharmacology Toxicology and PharmaceuticsMaleimideAlkylPharmacologychemistry.chemical_classificationSulfonylNucleophilic additionbiologyMolecular StructureOrganic ChemistryActive siteFluorineCycloadditionchemistrySpectrometry Mass Matrix-Assisted Laser Desorption-Ionizationbiology.proteinMolecular MedicineChemMedChem
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