Search results for "CLEAVAGE"

showing 10 items of 281 documents

Theoretical Elucidation of β-O-4 Bond Cleavage of Lignin Model Compound Promoted by Sulfonic Acid-Functionalized Ionic Liquid

2019

While the depolymerization of lignin to chemicals catalyzed by ionic liquids has attracted significant attention, the relevant molecular mechanism, especially the cleavage of specific bonds related to efficient depolymerization, still needs to be deeply understood for the complexity of this natural aromatic polymer. This work presents a detailed understanding of the cleavage of the most abundant β-O-4 bond in the model system, guaiacylglycerol β-guaiacyl ether, by a Brønsted acidic IL (1-methyl-3-(propyl-3-sulfonate) imidazolium bisulfate ([C3SO3Hmim][HSO4]) using density functional theory calculation and molecular dynamics simulation. It has been found that [C3SO3Hmim][HSO4] generates zwit…

Reaction mechanismligninProtonationEther02 engineering and technologySulfonic acid010402 general chemistry01 natural sciencesDFTlcsh:Chemistrychemistry.chemical_compoundComputational chemistryBond cleavageOriginal Researchionic liquidchemistry.chemical_classificationDepolymerizationGeneral Chemistry021001 nanoscience & nanotechnologymolecular dynamics0104 chemical sciencesChemistrychemistrylcsh:QD1-999ZwitterionIonic liquidβ-O-4 bondreaction mechanism0210 nano-technologyFrontiers in Chemistry
researchProduct

Synthesis of [18F]-Fluoroethylfenoterol for imaging β2 receptor status in lung in vivo

2001

5-(-{2-[4-(2-[18F]Fluoroethoxy)-phenyl]-l-methyl-ethylamino}-l-hydroxy-ethyl)-benzene-1, 3-diol ([18F]fluoroethylfenoterol) was synthesised from 4-(2-{benzyl-[2-(3,5-bis-benzyloxy-phenyl)-2-hydroxy-ethyl]-amino}-propyl)-phenol using 2-[18F]fluoroethyltosylate (92% RCY) followed by reductive cleavage of the benzyl protecting groups. Preliminary in vitro tests showed [19F]fluoroethylfenoterol to be as potent in relaxation of lung tissue as fenoterol itself.

Receptor StatusLungChemistryorganic chemicalsOrganic ChemistryBiochemistryIn vitroAnalytical Chemistrymedicine.anatomical_structureIn vivoReductive cleavageDrug Discoverypolycyclic compoundsmedicineBiophysicsRelaxation (physics)heterocyclic compoundsRadiology Nuclear Medicine and imagingLung tissueSpectroscopyFenoterolmedicine.drugJournal of Labelled Compounds and Radiopharmaceuticals
researchProduct

Hamster Bcl-2 Protein Is Cleaved in Vitro and in Cells by Caspase-9 and Caspase-3

2001

Full-length cDNA of hamster bcl-2 (771 nt) was cloned by RT-PCR and inserted into pGEX-4T-1 to produce the recombinant hamster Bcl-2 protein. The purified recombinant Bcl-2 protein (26.4 kDa) was used as a substrate for the active human caspase-3 and caspase-9 in vitro. It is shown here that Bcl-2 is efficiently cleaved by caspase-3 to a 23 kDa fragment. Although not possessing a putative caspase-9 cleavage site in its sequence, hamster Bcl-2 was also cleaved by caspase-9 into exactly the same 23 kDa cleavage product, indicating that cleavage occurred at the same site. Caspase-3- and caspase-9-mediated cleavage of Bcl-2 was efficiently blocked by caspase-3 (zDEVD) and caspase-9 (zLEHD) inhi…

Recombinant Fusion ProteinsBlotting WesternBiophysicsHamsterCaspase 3CHO CellsCysteine Proteinase InhibitorsCleavage (embryo)Biochemistrylaw.inventionlawCricetinaeComplementary DNAAnimalsHumansMolecular BiologyCaspaseGlutathione TransferaseCleavage stimulation factorbiologyCaspase 3Chinese hamster ovary cellThrombinCell BiologyCaspase InhibitorsMolecular biologyCaspase 9Proto-Oncogene Proteins c-bcl-2Caspasesbiology.proteinRecombinant DNAOligopeptidesBiochemical and Biophysical Research Communications
researchProduct

SAHA/TRAIL combination induces detachment and anoikis of MDA-MB231 and MCF-7 breast cancer cells

2012

Abstract SAHA, an inhibitor of histone deacetylase activity, has been shown to sensitize tumor cells to apoptosis induced by TRAIL, a member of TNF-family. In this paper we investigated the effect of SAHA/TRAIL combination in two breast cancer cell lines, the ERα−positive MCF-7 and the ERα−negative MDA-MB231. Treatment of MDA-MB231 and MCF-7 cells with SAHA in combination with TRAIL caused detachment of cells followed by anoikis, a form of apoptosis which occurs after cell detachment, while treatment with SAHA or TRAIL alone did not produce these effects. The effects were more evident in MDA-MB231 cells, which were chosen for ascertaining the mechanism of SAHA/TRAIL action. Our results show…

Recombinant Fusion ProteinsCellCASP8 and FADD-Like Apoptosis Regulating ProteinAntineoplastic AgentsBreast NeoplasmsHydroxamic AcidsCleavage (embryo)BiochemistryTNF-Related Apoptosis-Inducing LigandCell Line TumorProto-Oncogene ProteinsSettore BIO/10 - BiochimicaAntineoplastic Combined Chemotherapy ProtocolsCell AdhesionmedicineSAHA TRAIL Anoikis EGFR FAK BimELHumansAnoikisskin and connective tissue diseasesMda mb231VorinostatBcl-2-Like Protein 11ChemistryMembrane ProteinsGeneral MedicineAnoikisErbB ReceptorsGene Expression Regulation Neoplasticmedicine.anatomical_structureMCF-7ApoptosisCaspasesFocal Adhesion Kinase 1ImmunologyCancer researchPhosphorylationFemaleHistone deacetylase activityApoptosis Regulatory ProteinsSignal Transduction
researchProduct

Efficient DNA Cleavage Induced by Copper(II) Complexes of Hydrolysis Derivatives of 2,4,6‐Tri(2‐pyridyl)‐1,3,5‐triazine in the Presence of Reducing A…

2007

The reaction of 2,4,6-tri(pyridyl)-1,3,5-triazine (ptz) and copper(II) salts in dmf/water (1:1) results in the hydrolysis of ptz and formation of the anions bis(2-pyridylcarbonyl)amide (ptO2–) and bis(2-pyridylamine)amide (ptN2–), which are found in the complexes [Cu(ptN2)(OAc)]·3H2O (1), [Cu(ptO2)(OAc)(H2O)]·H2O (2), [Cu(ptN2)(for)]·3H2O (3) (for = formate), [Cu(ptO2)(for)(H2O)] (4), [Cu(ptO2)(benz)]·H2O (5) (benz = benzoate), and [Cu(ptO2)F(H2O)]2·3H2O (6). This report includes the chemical and spectroscopic characterization of all these complexes along with the crystal structures of 4–6. The coordination spheres of CuII in 4 and 5 are best described as distorted tetragonal square pyramid…

Reducing agentchemistry.chemical_elementCrystal structurePhotochemistryMedicinal chemistryCopperSquare pyramidal molecular geometryInorganic Chemistrychemistry.chemical_compoundchemistryAmideHydroxyl radicalBond cleavageCoordination geometryEuropean Journal of Inorganic Chemistry
researchProduct

Time-lapse technology: evaluation of embryo quality and new markers for embryo selection

2012

Current methods of embryo evaluation rely mainly on static observations of the embryo´s morphology. These observations are inevitably restricted to specific times and, considering that the development of the embryo is a dynamic process, several critical stages in between observations may go unnoticed. These methods are also very subjective, and variations between embryologists may affect critical decisions that will, in turn, affect the overall success of the IVF clinics. On the other hand, an increased number of multiple pregnancies calls for a reduction in the number of embryos transferred, making the selection procedure even more challenging for the embryologist. Therefore, new markers t…

Reproductive MedicineRisk analysis (engineering)Embryo cleavageembryonic structuresMaternity and MidwiferyPediatrics Perinatology and Child HealthObstetrics and GynecologyEmbryoAnatomyBiologyEmbryo qualitySelection (genetic algorithm)Expert Review of Obstetrics & Gynecology
researchProduct

DNA Oxidation Photoinduced by Norharmane Rhenium(I) Polypyridyl Complexes: Effect of the Bidentate N,N′-Ligands on the Damage Profile

2018

Re(I)--polypyridyl complexes have interesting and distinctive photochemical and photosensitizing properties. This work describes the capability to induce (or photoinduce) DNA damage of three Re(I)-complexes with a naturally occurring alkaloid called norharmane (nHo) as ligand: [Re(CO)₃ (nHo)(L)]CF₃ SO₃ where L=2,2'-bipyridine (ReBpy), phenanthroline (RePhen) or dipyrido[3,2-a:2',3'-c]phenazine (ReDppz). The interaction of the complexes with DNA was investigated by steady-state and time-resolved spectroscopy. Data show that the mode and strength of interaction depend on the chemical structure of the bidentate ligand. The complexes show a major static contribution to the overall interaction, …

Salmonella typhimuriumDenticityLightFísico-Química Ciencia de los Polímeros ElectroquímicaPhenanthrolineLigands01 natural sciences//purl.org/becyt/ford/1 [https]chemistry.chemical_compound22'-DipyridylStereochemistryCoordination ComplexesELECTRON TRANSFERSinglet OxygenCiencias QuímicasRHENIUMQuímicaChemistryRheniumPhotosensitizationPHOTOSENSITIZATIONAdductOxidation-ReductionCIENCIAS NATURALES Y EXACTASStereochemistryDNA damagePhenanthrolinePhenazineDNA CLEAVAGELigand010402 general chemistryCatalysisAdductElectron transferElectron transferAlkaloidsOxidants PhotochemicalPhenazine//purl.org/becyt/ford/1.4 [https]010405 organic chemistryLigandMutagenicity TestsDna cleavageOrganic ChemistryDenticityGeneral ChemistryDNA0104 chemical scienceschemistryALKALOIDSReactive Oxygen SpeciesDNACarbolinesDNA Damage
researchProduct

Potentialgesteuerte SS-Bindungsspaltung und Fluoreszenzmarkierungsstudien am Beispiel des Rinderinsulins

1985

Die drei SS-Brucken im Insulin konnen galvanostatisch unter Bildung der SH-A-Kette und der SH-B-Kette (Produktgemisch I) aufgespalten werden. Potentiostatisch gelingt bei -1.3 V (vs. SCE) die selektive Offnung der zwei interchenaren Disulfidbrucken (Produktgemisch II). Die vier SH-Gruppen im Produktgemisch II werden mit dem Vinylsulfon 1 blockiert (Produktgemisch III). Im Produktgemisch III wird die intrachenare Disulfidbrucke in der teilblockierten A-Kette bei -1.8 V (vs. SCE) potentiostatisch reduktiv geoffnet und mit dem fluoreszierenden Arylvinylsulfon 2 geschutzt (Produktgemisch IV). Auch die SH-Gruppen in den Produktgemischen I und II werden durch die fluoreszierenden Vinylsulfone 2 u…

Sh groupschemistry.chemical_compoundChemistryReductive cleavageArylOrganic ChemistryPolymer chemistryPhysical and Theoretical ChemistryVinyl sulfoneCleavage (embryo)FluorescenceLiebigs Annalen der Chemie
researchProduct

Sequence of the M28 dsRNA: Preprotoxin Is Processed to an α/β Heterodimeric Protein Toxin

1995

The killer and immunity phenotypes of K28 killer strains of Saccharomyces cerevisiae are determined by the 1.75-kb M28 dsRNA virus. In the plus strand, M28p, the K28 preprotoxin gene, comprises bases 13-1047 and is followed, after an additional 85 bases, by a 63-bp poly(A) sequence and a 553-base 3'-sequence. This 3'-sequence contains two potential stem-loop structures predicted to bind the L-A encoded cap-pol protein, initiating encapsidation; high-level expression results in curing of M1 dsRNA. Expression of M28p confers the complete K28 killer and immunity phenotype on a cell lacking M28 dsRNA. K28 toxin is a disulfide-bonded heterodimer of alpha (10.5 kDa) and beta (11 kDa) components w…

Signal peptideDNA ComplementaryGlycosylationSaccharomyces cerevisiae ProteinsGlycosylationMolecular Sequence DataMutantCarboxypeptidasesSaccharomyces cerevisiaeBiologymedicine.disease_causeCleavage (embryo)Fungal Proteinschemistry.chemical_compoundGene Expression Regulation FungalVirologyEndopeptidasesmedicineSecretionAmino Acid SequenceSubtilisinsGeneDNA PrimersRNA Double-StrandedBase SequenceToxinSerine EndopeptidasesMembrane ProteinsRNA FungalMycotoxinsMolecular biologyKiller Factors YeastRNA silencingchemistryProprotein ConvertasesProtein Processing Post-TranslationalVirology
researchProduct

Dissection of the structure-forming activity from the structure-guiding activity of silicatein: a biomimetic molecular approach to print optical fibe…

2020

Silicateins, a group of proteins forming the proteinaceous axial filaments of the inorganic biosilica spicules of the siliceous sponges, are unique in their dual function to exhibit both structure-guiding (providing the structural platform for the biosilica product) and structure-forming activities (enzymatic function: biosilica synthesis from ortho-silicate). The primary translation product of the silicatein gene comprises a signal peptide, a pro-peptide and, separated by an autocatalytic cleavage site glutamine/aspartic acid [Q/D], the sequence of the mature silicatein protein. In order to dissect the biocatalytic, structure-forming activity of silicatein from its structure-guiding functi…

Signal peptidechemistry.chemical_classificationbiologyBiomedical EngineeringWild typeSubstrate (chemistry)Sequence (biology)General ChemistryGeneral MedicineCleavage (embryo)biology.organism_classificationSuberites domunculaEnzymeBiochemistrychemistryAspartic acidGeneral Materials ScienceJournal of Materials Chemistry B
researchProduct