Search results for "language use"

showing 10 items of 5440 documents

The CEC behaviour of several synthetic peptides related to the activin ��A-��D subunits

2008

The resolution of several structurally related synthetic peptides, derived from the loop 3 region of the activin betaA-betaD subunits, has been studied using capillary electrochromatography (CEC) with Hypersil n-octadecylsilica as the sorbent. The results confirm that the CEC migration of these peptides can be varied in a charge-state-specific manner as the properties of the background electrolyte, such as pH, salt concentration and content of organic modifier, or temperature are systematically changed. Acidic peptides followed similar trends in retention behaviour, which was distinctly different to that shown by more basic peptides. The CEC separation of these peptides with the Hypersil n-…

chemistry.chemical_classificationCapillary electrochromatographySorbentChromatographyResolution (mass spectrometry)Salt (chemistry)Context (language use)ElectrolyteBiochemistrychemistry.chemical_compoundElectrophoresisEndocrinologychemistryAcetonitrileThe Journal of Peptide Research
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Chemical and enzymatic synthesis of glycopeptides

1995

Progress recently made in the synthesis of biologically relevant N- and O-glycopeptides is illustrated by examples. In this context, developments in the preparation of complex saccharide side chains and in the subsequent coupling to peptide portions is described. Special emphasis is given to the synthesis of Lewis antigen-type structures. Furthermore, modern methods in solid phase peptide syntheses utilizing glycosylated building blocks are presented. Recent advances in glycopeptide syntheses employing enzymatic methods in deprotection steps as well as in peptide/saccharide chain elongation are reported.

chemistry.chemical_classificationChemistrySide chainPeptideContext (language use)Enzymatic synthesisCombinatorial chemistryGlycopeptide
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Comperative studies with Culex pipiens egg rafts. Immunogenetic, electrophoretic and enzymatic analysis of unfertilized, compatible and incompatible …

1973

By applying immunologic, electrophoretic and enzymatic methods, extracts of different raft types of Culex pipiens were analysed. Rafts of the crosses Pa x Pa and Ha x Ha contained four common antigens, while unfertilized rafts of Pa and Ha (no antisera were prepared against them) and rafts of the crosses Og x Og, Og x Pa, and Pa x Og shared three common antigens with the remaining raft extracts. Disk-electrophoresis of raft extracts in acrylamide gel resulted in different electropherograms. Ten protein bands were common to all these raft types. The unfertilized rafts of Pa and Ha yielded three more protein bands, the crosses Pa x Ha and Ha x Pa one more, the crosses Og x Og and Pa x Og thre…

chemistry.chemical_classificationContext (language use)General MedicineRaftBiologyOuchterlony double immunodiffusionIsozymeMolecular biologyAminopeptidaseEnzymechemistryBiochemistryGeneticsAlkaline phosphataselipids (amino acids peptides and proteins)Agronomy and Crop SciencePolyacrylamide gel electrophoresisBiotechnologyTAG. Theoretical and applied genetics. Theoretische und angewandte Genetik
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Approaching an experimental electron density model of the biologically active trans ‐epoxysuccinyl amide group—Substituent effects vs. crystal packing

2017

The trans-epoxysuccinyl amide group as a biologically active moiety in cysteine protease inhibitors such as loxistatin acid E64c has been used as a benchmark system for theoretical studies of environmental effects on the electron density of small active ingredients in relation to their biological activity. Here, the synthesis and the electronic properties of the smallest possible active site model compound are reported to close the gap between the unknown experimental electron density of trans-epoxysuccinyl amides and the well-known function of related drugs. Intramolecular substituent effects are separated from intermolecular crystal packing effects on the electron density, which allows us…

chemistry.chemical_classificationElectron densitybiology010405 organic chemistryChemistryCarboxylic acidOrganic ChemistryIntermolecular forceSubstituentActive siteContext (language use)010402 general chemistry01 natural sciences0104 chemical sciencesCrystallographychemistry.chemical_compoundAmideIntramolecular forcebiology.proteinPhysical and Theoretical ChemistryJournal of Physical Organic Chemistry
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Mimicking photosynthesis: covalent [60]fullerene-based donor–acceptor ensembles

2004

Abstract Within the context of exploring photophysical properties of [60]fullerene-based donor–acceptor ensembles, we highlight in this contribution an approach towards the synthesis of a novel series of donor-bridge-acceptor, C 60 –wire– ex TTF , ensembles that incorporate p -phenylenevinylene oligomers, in which the conjugation length has been systematically increased, as bridges that connect π-extended tetrathiafulvalenes (exTTF) (electron donor) with [60]fullerene (electron acceptor). This molecular design allows probing the effects of distance and rate, at which electron transfer processes occur, as well as the molecular-wire behavior of the oligo-PPV fragments.

chemistry.chemical_classificationFullereneChemistryMechanical EngineeringMetals and AlloysContext (language use)Electron donorSettore CHIM/06 - Chimica OrganicaElectron acceptorCondensed Matter PhysicsPhotochemistryPhotoinduced electron transferElectronic Optical and Magnetic MaterialsMolecular wireElectron transferchemistry.chemical_compoundFullerene derivativesMechanics of MaterialsMaterials ChemistryTetrathiafulvaleneSynthetic Metals
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Investigations Concerning the Correlation of COX-1 Inhibitory and Hydroxyl Radical Scavenging Activity

2008

The aim was to study the COX-1 inhibiting efficacy in context with hydroxyl radical scavenging properties of compounds bearing a carboxylic acid and ester function, respectively. In general, the acids are more potent radical scavengers than the corresponding esters but there is no clear correlation with their COX-1 inhibiting potencies. A feasible scavenging mechanism of carboxylic acids is discussed.

chemistry.chemical_classificationHydroxyl RadicalRadicalCarboxylic acidPharmaceutical ScienceContext (language use)Free Radical ScavengersInhibitory postsynaptic potentialStructure-Activity Relationshipchemistry.chemical_compoundchemistryDrug DiscoveryCyclooxygenase 1AnimalsOrganic chemistryCattleCyclooxygenase InhibitorsHydroxyl radicalScavengingArchiv der Pharmazie
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Functional Nanohybrids Based on Dyes and Upconversion Nanoparticles

2020

Upconversion nanoparticles (UCNPs) and dyes are combined to make nanohybrid systems, which take advantage of the synergic relationship between lanthanide (Ln)-based UCNPs and dyes. Ln-UCNPs are inorganic nanophosphors which absorb NIR light and emit narrow emission bands in the UV-NIR region with long luminescence lifetimes. These unique properties, when coordinated properly with dyes of the appropriate photophysical features, produce nanosystems with new photophysical properties. In this context, the UCNP-dye nanohybrids are very promising for potential sensing (ions and biomolecules) and theragnosis (imaging and therapy, e.g. photodynamic therapy).

chemistry.chemical_classificationLanthanideUpconversion nanoparticlesMaterials scienceNir lightchemistryBiomoleculemedicine.medical_treatmentmedicineContext (language use)NanotechnologyPhotodynamic therapyLuminescence
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2021

Ruthenium(II) polypyridine complexes are among the most popular sensitizers in photocatalysis, but they face some severe limitations concerning accessible excited-state energies and photostability that could hamper future applications. In this study, the borylation of heteroleptic ruthenium(II) cyanide complexes with alpha-diimine ancillary ligands is identified as a useful concept to elevate the energies of photoactive metal-to-ligand charge-transfer (MLCT) states and to obtain unusually photorobust compounds suitable for thermodynamically challenging energy transfer catalysis as well as oxidative and reductive photoredox catalysis. B(C6F5)(3) groups attached to the CN- ligands stabilize t…

chemistry.chemical_classificationPhotoisomerization010405 organic chemistryChemistryPinacolPhotoredox catalysischemistry.chemical_elementContext (language use)010402 general chemistryPhotochemistry01 natural sciencesBorylation0104 chemical sciencesCoordination complexRutheniumCatalysischemistry.chemical_compoundJACS Au
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Characterization of HLA-DR- and TCR-binding residues of an immunodominant and genetically permissive peptide of the 16-kDa protein of Mycobacterium t…

2004

The 16-kDa protein of Mycobacterium tuberculosis represents an important antigenic target during bacillary latency and, consequently, should be considered as candidate subunit vaccine component. In this study, we have used CD4 T cell clones that recognize the peptide p91-110, an immunodominant and genetically permissive epitope, in the context of five different HLA-DR molecules and truncated and substituted variants of this peptide, to identify the minimal binding sequence (HLA-DR-binding core) and the minimal stimulatory sequence (TCR-binding core), as well as the residues that contact HLA-DR molecules and the TCR. We have found a common 9-mer sequence, spanning amino acids 93-101, as the …

chemistry.chemical_classificationProtein subunitT-LymphocytesImmunologyT-cell receptorReceptors Antigen T-CellContext (language use)PeptideHuman leukocyte antigenHLA-DR AntigensMycobacterium tuberculosisBiologyMolecular biologyEpitopeAmino acidchemistryPepscanBacterial ProteinsImmunology and AllergyHumansPeptidesEuropean journal of immunology
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The Role of Mitochondrial Reactive Oxygen Species Formation for Age-Induced Vascular Dysfunction

2010

Aging is an important risk factor for the development of cardiovascular diseases, which can be accelerated by atherosclerosis, diabetes, hypercholesterolemia, or obesity. Vascular aging is mainly characterized by endothelial dysfunction, an alteration of endothelium-dependent signaling processes, and vascular remodeling. The underlying mechanisms include increased production of reactive oxygen species (ROS), inactivation of nitric oxide (•NO), and subsequent formation of reactive nitrogen and oxygen species (RNOS). Elevated RNOS may exhibit new messenger functions by posttranslational oxidative modification of intracellular regulatory proteins or lead to irreversible alterations of biologic…

chemistry.chemical_classificationReactive oxygen speciesChemistryContext (language use)Oxidative phosphorylationMitochondrionmedicine.diseaseNitric oxideCell biologychemistry.chemical_compoundDiabetes mellitusmedicineEndothelial dysfunctionIntracellular
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