Search results for "Reversible"

showing 10 items of 140 documents

Mutations in the Bacillus thuringiensis Cry1Ca toxin demonstrate the role of domains II and III in specificity towards Spodoptera exigua larvae

2004

Several mutants of the Bacillus thuringiensis Cry1Ca toxin affected with regard to specific activity towards Spodoptera exigua were studied. Alanine was used to replace single residues in loops 2 and 3 of domain II (mutant pPB19) and to replace residues 541– 544 in domain III (mutant pPB20). Additionally, a Cry1Ca mutant combining all mutations was constructed (mutant pPB21). Toxicity assays showed a marked decrease in toxicity against S. exigua for all mutants, while they retained their activity against Manduca sexta, confirming the importance of these residues in determining insect specificity. Parameters for binding to the specific receptors in BBMV (brush border membrane vesicles) of S.…

Models MolecularMutantLaboratory of Virologyaminopeptidase nmedicine.disease_causeBiochemistrybrush-border membraneToxin oligomerizationSubstrate SpecificityBacterial toxin; Manduca sexta; Mode of action; Protoxin activation; Toxin oligomerization; Toxin receptor bindingHemolysin Proteinsmanduca-sextaBacillus thuringiensisheliothis-virescensAlanine:CIENCIAS DE LA VIDA::Bioquímica [UNESCO]MicrovillibiologyPRI BioscienceBiochemistryMode of actionLarvaThermodynamicsResearch ArticleProtein BindingBacterial Toxinspink-bollwormBacillus thuringiensisSpodopteraSpodopteraBinding CompetitiveManduca sextaLaboratorium voor VirologieBacterial ProteinsExiguamedicineirreversible bindingAnimalscrystal proteinsProtoxin activationProtein Structure QuaternaryMode of actionMolecular BiologyBacillus thuringiensis ToxinsToxin receptor bindingToxininsecticidal toxinpore formationCytoplasmic VesiclesfungiUNESCO::CIENCIAS DE LA VIDA::BioquímicaBacterial toxinCell Biologybiology.organism_classificationProtein Structure TertiaryEndotoxinsManduca sextaMutationcryia delta-endotoxins
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Activation of self-renewal and meiotic genes in tumour cell lines resistant to genotoxic treatment

2014

Pašatjaunošanās un meijotisko gēnu aktivācija pēc genotoksiskas apstrādes rezistentās audzēju šūnu līnijās Šajā darbā tika pētīta iespējamā saistība starp poliploīdijas un dzimumšūnu līnijai raksturīgo gēnu indukciju pēc pretvēža apstrādes atkarībā no TP53 statusa un audzēju šūnu rezistence pret DNS bojājumu. Pirmo reizi tika atrasta un citoloģiski raksturota galveno cilmestības transkripcijas faktoru OCT4, NANOG un SOX2 ekspresijas aktivācija, kas izraisīta pārkāpjot tetraploīdo barjeru pēc DNS bojājuma TP53 mutantās, bet ne funkcionālās audzēja šūnas, kā arī galvenā mejotiskā kohezīna REC8 ekspresija somatisko audzēja šūnu līnijās, kas apstrādātas ar jonizējošo starojumu vai topoizomeraze…

Molecular Biology and Biochemistryreversible polyploidyatgriezeniska poliploīdijaembrionālo cilmes šūnu gēnilymphoma cell lineslimfomu šūnu līnijasDNA damageDzīvās dabas zinātnesBioloģijaDNS bojājumsembryonal stem cell genes
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1993

Nitroxide mediated radical polymerizationAnionic addition polymerizationPolymerizationChemistryPolymer chemistryRadical polymerizationChain transferReversible addition−fragmentation chain-transfer polymerizationPhotochemistryIonic polymerizationLiving anionic polymerizationDie Makromolekulare Chemie, Rapid Communications
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Star-Like Polymers of tert -Butyl Acrylate via Controlled Radical Polymerization - Synthesis and Properties

2011

Summary: Star polymers with different numbers and lengths of poly(tert-butyl acrylate) arms were obtained by the core-first method via atom transfer and iodine mediated radical polymerization. Multifunctional initiators with different numbers of initiating groups (from 3 to 28) were used to initiate the polymerization of tert-butyl acrylate, yielding stars with different numbers of arms. The structures of the stars were characterized by NMR and gel permeation chromatography with refractive index, multiangle laser light scattering and viscosimetric detectors.

Nitroxide mediated radical polymerizationMaterials sciencePolymers and PlasticsOrganic ChemistryRadical polymerizationChain transferCondensed Matter PhysicsPhotochemistryLiving free-radical polymerizationPolymerizationPolymer chemistryMaterials ChemistryCoordination polymerizationReversible addition−fragmentation chain-transfer polymerizationIonic polymerizationMacromolecular Symposia
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Tailored Semiconducting Polymers: Living Radical Polymerization and NLO-Functionalization of Triphenylamines

2002

This paper describes the preparation of various polymers with triarylamine side groups. High molecular weight materials were obtained by free radical polymerization utilizing the gel effect. Polymers with a marrow polydispersity and a predetermined molecular weight could be prepared by living radical polymerization. The T g could, thereby, be controlled between 50 and 140°C either by using different monomers or by varying the molecular weight. Living radical polymerization allowed in addition the preparation of block copolymers. The triarylamine side groups could be transformed into NLO-chromophores by reaction with tetracyanoethylene. This leads to the incorporation of tricyanoethylene. Th…

Nitroxide mediated radical polymerizationPolymers and PlasticsChemistryOrganic ChemistryRadical polymerizationChain transferCondensed Matter PhysicsLiving free-radical polymerizationPolymerizationPolymer chemistryMaterials ChemistryLiving polymerizationReversible addition−fragmentation chain-transfer polymerizationPhysical and Theoretical ChemistryIonic polymerizationMacromolecular Chemistry and Physics
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Cyclodextrins in Polymer Synthesis:  Free-Radical Polymerization of Methylated β-Cyclodextrin Complexes of Methyl Methacrylate and Styrene Controlled…

2000

Nitroxide mediated radical polymerizationPolymers and PlasticsChemistryOrganic ChemistryRadical polymerizationChain transferInorganic ChemistryEnd-groupLiving free-radical polymerizationPolymerizationPolymer chemistryMaterials ChemistryLiving polymerizationReversible addition−fragmentation chain-transfer polymerizationMacromolecules
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How the interplay of different control mechanisms affects the initiator efficiency factor in controlled radical polymerization: An investigation usin…

2007

International audience; Compound CpMoI2(iPr2dad) (iPr2dad = iPrNdouble bondCHsingle bondCHdouble bondNiPr), obtained by halide exchange from CpMoCl2(iPr2dad) and NaI, has been isolated and characterized by EPR spectroscopy, cyclic voltammetry, and X-ray crystallography. Its action as a catalyst in atom transfer radical polymerization (ATRP) and as a spin trap in organometallic radical polymerization (OMRP) of styrene and methyl acrylate (MA) monomers has been investigated and compared with that of the dichloro analogue. Compound CpMoCl2(iPr2dad) catalyzes the ATRP of styrene and MA with low efficiency factors f (as low as 0.37 for MA and ethyl 2-chloropropionate as initiator), while it irre…

Nitroxide mediated radical polymerizationRadical polymerizationAtom transfer010402 general chemistryPhotochemistry01 natural sciencesBiochemistryOne-electron oxidative additionStyreneInorganic Chemistrychemistry.chemical_compoundLiving free-radical polymerizationPolymer chemistryMaterials ChemistryReversible addition−fragmentation chain-transfer polymerization[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryMethyl acrylateControlled radical polymerizationMolybdenum010405 organic chemistryChemistryAtom-transfer radical-polymerizationOrganic Chemistry[CHIM.CATA]Chemical Sciences/Catalysis0104 chemical sciences[CHIM.POLY]Chemical Sciences/PolymersCobalt-mediated radical polymerizationInitiator efficiency factor
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HEAT FLUX IN SUPERFLUID TRANSITION AND IN TURBULENT HELIUM COUNTERFLOW

Normal fluid profileRadial flow Vortex diffusionTwo-fluid modelHelium 4Ballistic regimeInhomogeneous vortex tangles.lambda TransitionHeat transferQuantized vorticeEffective thermal conductivityTurbulent superfluid helium ( He II)One-fluid modelExtended Irreversible ThermodynamicEntrance regionSettore MAT/07 - Fisica MatematicaLongitudinal flow
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Vemurafenib and cobimetinib combination therapy for BRAFV600E-mutated melanoma favors posterior reversible encephalopathy syndrome

2019

OncologyCobimetinibmedicine.medical_specialtyCombination therapybusiness.industryMelanomaPosterior reversible encephalopathy syndromeHematologymedicine.diseasechemistry.chemical_compoundText miningOncologychemistryInternal medicinemedicineVemurafenibbusinessmedicine.drugAnnals of Oncology
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P(HPMA)-block-P(LA) copolymers in paclitaxel formulations: Polylactide stereochemistry controls micellization, cellular uptake kinetics, intracellula…

2012

In order to explore the influence of polymer microstructure and stereochemistry in biological settings, the synthesis, micellization, cellular fate and the use in paclitaxel formulations of poly(N-(2-hydroxypropyl)-methacrylamide)-block-poly(L-lactide) (P(HPMA)-block-P(LLA)) and poly(N-(2-hydroxypropyl)-methacrylamide)-block-poly(DL-lactide) block copolymers (P(HPMA)-block-P(DLLA)) were studied. To this end, P(HPMA)-block-P(lactide) block copolymers and their fluorescently labeled analogues were synthesized. The polymers exhibited molecular weights M-n around 20,000 g/mol with dispersities (D=M-w/M-n) below 1.3. In addition, the solution conformation of this new type of partially degradable…

PaclitaxelStereochemistryCell SurvivalPolyestersTacticityMolecular ConformationPharmaceutical ScienceMicellechemistry.chemical_compoundTacticityAmphiphilePolymer chemistryPolylactide block copolymersCopolymerHumansReversible addition−fragmentation chain-transfer polymerizationMicelleschemistry.chemical_classificationLactideRAFT polymerizationPoly(N-(2-hydroxypropyl)-methacrylamideBiological TransportPolymerStructure activity relationshipAntineoplastic Agents PhytogenicKineticschemistryDrug deliveryHPMA block copolymersMethacrylatesHeLa Cells
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