Search results for "affinity"

showing 10 items of 313 documents

Unveiling species assemblage rules in gypsum plant communities

2023

Plant communities are not merely snapshots of species located in the same area. Instead, they are dynamic entities connected through complex biotic interactions. Understanding the interplay of processes that bind species within a community is vital for comprehending species maintenance and may assist us in predicting how communities respond to the perturbations of a changing world. This Ph.D. aims to unveil how abiotic conditions, plant strategies, and biotic interactions shape plant communities growing in stressful environments. Plant species can thrive in stressful environments through contrasted strategies, either showing species-specific adaptive strategies or reliance on facilitative i…

UNESCO::CIENCIAS DE LA VIDA::Biología vegetal (Botánica) ::Ecología vegetalrewiringcontrasting stressphylogenynursesgypsumgypsum affinitylimestonefacilitationneighborhoodplant communities
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Heparin-binding protein targeted to mitochondrial compartments protects endothelial cells from apoptosis.

1999

Neutrophil-borne heparin-binding protein (HBP) is a multifunctional protein involved in the progression of inflammation. HBP is stored in neutrophil granules and released upon stimulation of the cells in proximity to endothelial cells. HBP affects endothelial cells in multiple ways; however, the molecular and cellular mechanisms underlying the interaction of HBP with these cells are unknown. Affinity isolation and enzymatic degradation demonstrated that HBP released from human neutrophils binds to endothelial cell-surface proteoglycans, such as syndecans and glypican. Flow cytometry indicated that a significant fraction of proteoglycan-bound HBP is taken up by the endothelial cells, and we …

Umbilical VeinsEndotheliumCell SurvivalNeutrophilsmedia_common.quotation_subjectmedicine.medical_treatmentInflammationApoptosisBiologyFibroblast growth factorLeukotriene B4ArticleChromatography AffinityFlow cytometryParacrine CommunicationLeukocytesmedicineAnimalsHumansInternalizationCells Culturedmedia_commonInflammationmedicine.diagnostic_testHeparinMonocyteGrowth factorBiological TransportGeneral MedicineBlood ProteinsMolecular biologyRecombinant ProteinsMitochondriaN-Formylmethionine Leucyl-PhenylalanineKineticsmedicine.anatomical_structureApoptosisCommentaryTetradecanoylphorbol AcetateProteoglycansEndothelium Vascularmedicine.symptomCarrier ProteinsAntimicrobial Cationic PeptidesThe Journal of clinical investigation
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Alien flora of Europe: Species diversity, temporal trends, geographical patterns and research needs

2008

International audience; The paper provides the first estimate of the composition and structure of alien plants occurring in the wild in the European continent, based on the results of the DAISIE project (2004–2008), funded by the 6th Framework Programme of the European Union and aimed at “creating an inventory of invasive species that threaten European terrestrial, freshwater and marine environments”. The plant section of the DAISIE database is based on national checklists from 48 European countries/regions and Israel; for many of them the data were compiled during the project and for some countries DAISIE collected the first comprehensive checklists of alien species, based on primary data …

[SDE] Environmental SciencesALIEN PLANTSBIOGEOGRAPHICAL PATTERN[SDV]Life Sciences [q-bio]RESIDENCE TIMEDONOR REGIONS[SDV] Life Sciences [q-bio]biogeographical pattern; plant invasions; temporal trends; europe; habitat affinity; alien plants; naturalization; residence time; neophytes; donor regionsTEMPORAL TRENDS[SDE]Environmental SciencesHABITAT AFFINITYeuropeNATURALIZATIONPLANT INVASIONSNEOPHYTES
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Calcium, calmodulin-dependent protein phosphorylation in Neurospora crassa

1984

Abstract A calcium, calmodulin-dependent protein kinase activity has been partially purified by calmodulin-Sepharose affinity chromatography from the soluble fraction of Neurospora crassa . The phosphorylated peptide has an apparent molecular mass on SDS-polyacrylamide gel of 47 kDa. The apparent half maximal phosphorylation is obtained after 1.5 min at 30° C in the presence of calcium and calmodulin. The apparent half maximal activation of the phosphorylation is obtained at 1 μM calcium, and 0.1 or 0.2 μM calmodulin from bovine brain or Neurospora , respectively. The 32 P incorporation is enhanced about 10-fold by calmodulin.

[SDE] Environmental SciencesCalmodulin[SDV]Life Sciences [q-bio]Biophysicschemistry.chemical_elementCalciumBiochemistryNeurosporaProtein kinaseNeurospora crassa03 medical and health sciencesAffinity chromatographyCalmodulinStructural BiologyGenetics[SDV.BV]Life Sciences [q-bio]/Vegetal BiologyProtein phosphorylation[SDV.BV] Life Sciences [q-bio]/Vegetal BiologyProtein kinase AMolecular BiologyComputingMilieux_MISCELLANEOUS030304 developmental biology0303 health sciencesbiologyNeurospora crassa030306 microbiologyCell Biologybiology.organism_classification[SDV] Life Sciences [q-bio]chemistryBiochemistry[SDE]Environmental Sciencesbiology.proteinPhosphorylationCalcium
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Actin in Allomyces arbuscula

1991

International audience; A 42 kDa protein was isolated by affinity chromatography on DNAse I-Sepharose from 24-h-old mycelia of Allomyces arbuscula. It was identified as actin by immunoblots with monoclonal antibody probe against a chicken gizzard actin. This fungal actin has a pI of 5.9 and separates into two spots on two-dimensional polyacrylamide gel electrophoresis, suggesting its dual nature. It can polymerize into 8-10 nm filaments visualized by electron microscopy.

[SDE] Environmental Sciencesmedicine.drug_classAllomyces[SDV]Life Sciences [q-bio]Plant Sciencemacromolecular substancesMonoclonal antibodylaw.invention03 medical and health sciencesAffinity chromatographylawGeneticsmedicine[SDV.BV]Life Sciences [q-bio]/Vegetal Biology[SDV.BV] Life Sciences [q-bio]/Vegetal BiologyPolyacrylamide gel electrophoresisEcology Evolution Behavior and SystematicsActin030304 developmental biologyGel electrophoresis0303 health sciencesbiology030306 microbiologybiology.organism_classificationMolecular biologyActina[SDV] Life Sciences [q-bio]Biochemistry[SDE]Environmental SciencesElectron microscopeBiotechnology
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Reinforcing willingness to buy and to pay due to consumer affinity towards a foreign country

2014

International audience; In a tense economic environment where consumers are encouraged to favor local rather than imported products, multinational companies (MNEs) need leverage to enhance their offer regarding local products. This research suggests a consideration of consumer affinity towards a foreign country as a means to reinforce both willingness to buy (WTB) and willingness to pay (WTP). An experiment was conducted with 170 French consumers (non-students). Respondents were asked about their WTB and their WTP for products for which the country of origin varied in a within-subject design based on 1) the level of the respondent's sense of affinity towards the product’s country of origin …

[SHS.GESTION]Humanities and Social Sciences/Business administrationconsumer affinitywillingness to buy[SHS.GESTION] Humanities and Social Sciences/Business administrationinternational marketing[ SHS.GESTION ] Humanities and Social Sciences/Business administrationwillingness to paycountry-image
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A factor derived from chick embryo retina which inhibits DNA synthesis of retina itself.

1992

Chick embryo retinas contain a peptide factor that inhibits DNA synthesis in explants of chick embryo retina. The inhibitory factor, obtained by acid/ethanol extraction from 15-day-old chick embryo retinas, was partially purified by affinity chromatography on heparin-sepharose CL-6B and gel filtration on Sephadex G-100. The inhibitor reduced DNA synthesis with maximal effects observed in retinal explants from 7 to 8-day-old chick embryos. The inhibitory effect became apparent after 10 h of incubation and reached the maximum levels after 16 h. DNA-inhibiting activity was heat and acid-stable and was destroyed by trypsin and alkaline treatments. The inhibitory effect was observed in retinal e…

animal structuresChick EmbryoBiologyBiochemistryChromatography AffinityRetinaCellular and Molecular Neurosciencechemistry.chemical_compoundBiological Factorsinhibits DNA synthesisAffinity chromatographyCulture TechniquesmedicineAnimalsRetinaDNA synthesisTissue ExtractsEmbryogenesisEmbryoGeneral MedicineDNATrypsinMolecular biologymedicine.anatomical_structureBiochemistrychemistrySephadexembryonic structuresChromatography GelThymidineCell Divisionmedicine.drugThymidineNeurochemical research
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Expression and purification of polyhistidine-tagged firefly luciferase in insect cells

2001

The coleopteran firefly, Photinus pyralis, luciferase was produced in lepidopteran Trichoplusia ni insect cells using a baculovirus expression vector. The recombinant protein was equipped with a polyhistidine affinity tag at the carboxyl terminus and purified by immobilized metal-ion affinity chromatography in combination with an expanded bed adsorption system. This approach enabled an efficient, one-step purification protocol of a genetically modified luciferase with properties similar to those of the authentic counterpart. According to light emission measurements, the final yield of highly purified protein was 23 mg l−1 of cell culture. In addition, no specific interaction of interfering …

aviationRecombinant Fusion ProteinsBioengineeringMothsProtein EngineeringApplied Microbiology and Biotechnologychemistry.chemical_compoundAffinity chromatographyPhotinus pyralisAnimalsLuciferaseHistidinePolyhistidine-tagLuciferasesbiologyExpanded bed adsorptionGeneral Medicinebiology.organism_classificationFusion proteinMolecular biologyColeopteraaviation.aircraft_modelchemistryBiochemistryLight emissionLampyridaePeptidesBiotechnologyJournal of Biotechnology
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Identification of glucan-mannoprotein complexes in the cell wall of Candida albicans using a monoclonal antibody that reacts with a (1,6)- -glucan ep…

1995

The use of a novel monoclonal antibody (mAb) that reacts with (1,6)-beta-glucan has permitted the study of the different covalent linkages between glucan and mannoproteins in the cell wall of Candida albicans. The mAb JRR1 was originally raised by immunization with Zymolyase extracts from C. albicans cell walls, but it soon became apparent that it reacted with a (1,6)-beta-glucan epitope. By using this antibody, we show the existence of glucan-mannoprotein complexes between the (1,6)-beta-glucan epitope recognized by the antibody and cell wall mannoproteins. The topology of the (1,6)-beta-glucan in the cell wall of C. albicans has also been studied.

beta-Glucansmedicine.drug_classFluorescent Antibody Techniquemacromolecular substancesMonoclonal antibodyBinding CompetitiveMicrobiologyChromatography AffinityEpitopeMicrobiologyFungal ProteinsMannansCell wallEpitopesAntigenCell WallPolysaccharidesCandida albicansmedicineCandida albicansGlucansGlucanchemistry.chemical_classificationMembrane GlycoproteinsbiologyTunicamycinAntibodies Monoclonalbiology.organism_classificationCorpus albicanscarbohydrates (lipids)stomatognathic diseaseschemistrybiology.proteinAntibodyMicrobiology
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Chemical Proteomics-Guided Identification of a Novel Biological Target of the Bioactive Neolignan Magnolol

2019

Understanding the recognition process between bioactive natural products and their specific cellular receptors is of key importance in the drug discovery process. In this outline, some potential targets of Magnolol, a natural bioactive compound, have been identified by proteomic approaches. Among them, Importin-β1 has been considered as the most relevant one. A direct binding between Magnolol and this nuclear chaperone has been confirmed by DARTS and molecular docking, while its influence on Importin-β1 translocation has been evaluated by in vitro assays.

bioactive neolignans02 engineering and technologyComputational biology010402 general chemistryProteomics01 natural scienceslcsh:Chemistrychemistry.chemical_compoundchemical proteomicsdrug affinity responsive target stabilityOriginal Researchbioactive neolignans; chemical proteomics; drug affinity responsive target stability; molecular docking; nuclear importbiologyChemistryDrug discoveryIn vitro toxicologyGeneral Chemistrymolecular docking021001 nanoscience & nanotechnologynuclear importMagnololBioactive compound0104 chemical sciencesChemistrylcsh:QD1-999Biological targetChaperone (protein)Direct bindingbiology.protein0210 nano-technologyFrontiers in Chemistry
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