Search results for "CD"

showing 10 items of 4072 documents

Interaction between 24-hydroxycholesterol, oxidative stress, and amyloid-β in amplifying neuronal damage in Alzheimer’s disease: three partners in cr…

2011

All three cholesterol oxidation products implicated thus far in the pathogenesis of Alzheimer's disease, 7β-hydroxycholesterol, 24-hydroxycholesterol, and 27-hydroxycholesterol, markedly enhance the binding of amyloid-beta (Aβ) to human differentiated neuronal cell lines (SK-N-BE and NT-2) by up-regulating net expression and synthesis of CD36 and β1-integrin receptors. However, only 24-hydroxycholesterol markedly potentiates the pro-apoptotic and pro-necrogenic effects of Aβ(1-42) peptide on these cells: 7β-hydroxycholesterol and 27-hydroxycholesterol, like unoxidized cholesterol, show no potentiating effect. This peculiar behavior of 24-hydroxycholesterol at physiologic concentrations (1 μ…

chemistry.chemical_classificationAgingReactive oxygen speciesbiologyCD36NeurotoxicityLong-term potentiationCell BiologyGlutathionemedicine.diseasemedicine.disease_causeCell biologychemistry.chemical_compoundchemistryBiochemistrypolycyclic compoundsbiology.proteinmedicinelipids (amino acids peptides and proteins)ReceptorOxidative stressIntracellularAging Cell
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Cloning and expression of two novel aldo-keto reductases fromDigitalis purpurealeaves

2002

The aldo-keto reductase (AKR) superfamily comprises proteins that catalyse mainly the reduction of carbonyl groups or carbon–carbon double bonds of a wide variety of substrates including steroids. Such types of reactions have been proposed to occur in the biosynthetic pathway of the cardiac glycosides produced by Digitalis plants. Two cDNAs encoding leaf-specific AKR proteins (DpAR1 and DpAR2) were isolated from a D. purpurea cDNA library using the rat Δ4-3-ketosteroid 5β-reductase clone. Both cDNAs encode 315 amino acid proteins showing 98.4% identity. DpAR proteins present high identities (68–80%) with four Arabidopsis clones and a 67% identity with the aldose/aldehyde reductase from Medi…

chemistry.chemical_classificationAldo-keto reductasecDNA libraryReductaseBiologyBiochemistryAmino acidchemistry.chemical_compoundEnzymeBiochemistrychemistryBiosynthesisGene expressionAldehyde ReductaseEuropean Journal of Biochemistry
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O44. Inhibition of CD98-associated amino acid transporters by dinitrosyl iron complexes

2008

chemistry.chemical_classificationCancer ResearchCD98BiochemistrybiologyPhysiologyChemistryClinical Biochemistrybiology.proteinTransporterBiochemistryAmino acidNitric Oxide
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Improved detection of melanoma antigen-specific T cells expressing low or high levels of CD8 by HLA-A2 tetramers presenting a Melan-A/Mart-1 peptide …

2001

MHC class I tetramers containing peptide epitopes are sensitive tools for detecting antigen-specific CD8(+) T-cell responses. We demonstrate here that binding of HLA-A2 tetramers to CD8(+) T cells specific for the melanoma-associated antigen Melan-A/MART-1 can be fine-tuned by altering either the bound peptide epitope or residues in the alpha 3 domain of HLA-A2, which is important for CD8 binding. Antigen-specific T cells expressing high levels of CD8 could be detected using HLA-A2 tetramers containing the peptide AAGIGILTV, an epitope which is naturally processed and presented from Melan-A/MART-1. In contrast, low CD8-expressing, antigen-specific T cells could be detected efficiently only …

chemistry.chemical_classificationCancer ResearchbiologyT-cell receptorPeptideMHC restrictionVirologyMolecular biologyEpitopeOncologychemistryAntigenMHC class IMART-1 Antigenbiology.proteinCD8International Journal of Cancer
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Putative multiadhesive protein from the marine spongeGeodia cydonium: Cloning of the cDNA encoding a fibronectin-, an SRCR-, and a complement control…

1998

Sponges (Porifera) representing the simplest metazoan phylum so far have been thought to possess no basal lamina tissue structures. One major extracellular matrix protein that is also a constitutive glycoprotein of the basal lamina is fibronectin. It was the aim of the present study to identify the native protein from the marine sponge Geodia cydonium and to isolate the corresponding cDNA. In crude extracts from this sponge protein(s) of Mr of Ý230 and Ý210 kDa could be visualized by Western blotting using an anti-fibronectin [human] antibody. By PCR cloning from a cDNA library of G. cydonium we isolated a cDNA comprising one element of fibronectin, the type-III (FN3) module. The cDNA (2.3 …

chemistry.chemical_classificationCloningbiologycDNA libraryGeneral Medicinebiology.organism_classificationMolecular biologyAmino acidFibronectinSpongechemistryComplementary DNAbiology.proteinAnimal Science and ZoologyGlycoproteinComplement control proteinThe Journal of Experimental Zoology
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Tryptophan catabolism via kynurenine production in Streptomyces coelicolor: identification of three genes coding for the enzymes of tryptophan to ant…

2011

Most enzymes involved in tryptophan catabolism via kynurenine formation are highly conserved in Prokaryotes and Eukaryotes. In humans, alterations of this pathway have been related to different pathologies mainly involving the central nervous system. In Bacteria, tryptophan and some of its derivates are important antibiotic precursors. Tryptophan degradation via kynurenine formation involves two different pathways: the eukaryotic kynurenine pathway, also recently found in some bacteria, and the tryptophan-to-anthranilate pathway, which is widespread in microorganisms. The latter produces anthranilate using three enzymes also involved in the kynurenine pathway: tryptophan 2,3-dioxygenase (TD…

chemistry.chemical_classificationKynurenine pathwayCatabolismHydrolasesStreptomyces coelicolorTryptophanTryptophanTryptophan Kynurenine S. coelicolor CDAStreptomyces coelicolorGeneral MedicineBiologybiology.organism_classificationApplied Microbiology and BiotechnologyTryptophan Oxygenasechemistry.chemical_compoundKynureninaseEnzymechemistryBiochemistryArylformamidaseIndoleamine 23-dioxygenaseKynurenineKynurenineMetabolic Networks and PathwaysBiotechnology
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Interaction of 5‐fluorouracil with β‐cyclodextrin: A density functional theory study with dispersion correction

2020

Detailed studies on the stability, interaction, and microstructure of host‐guest complexes in the vacuum of 5‐fluorouracil (5FU) with β‐cyclodextrin (βCD) were performed using B3LYP with the inclusion of Grimme's dispersion correction GD3 term and 6‐31+G(d,p) basis set. Among several studied 1:1 5FU‐βCD complexes, the one placing the keto tautomer of 5FU vertically in the host cavity and forming N‐H···OCD and CO···HOCD hydrogen bonds with hydroxyl groups of the smaller rim of βCD has the highest stability (Eint = −195 kJ/mol). Interestingly, there are no interactions with the inner hydrophobic part of the βCD host cavity. The strength of the intermolecular H‐bonds to the smaller rim of βC…

chemistry.chemical_classificationMaterials scienceCyclodextrinInteraction energyCondensed Matter Physics5‐fluorouracil (5FU)Atomic and Molecular Physics and OpticsDFT‐D3β‐cyclodextrin (βCD)chemistryChemical physicsDispersion (optics)Density functional theoryPhysical and Theoretical Chemistryinclusion complexinteraction energyInternational Journal of Quantum Chemistry
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Impact of amino acids 22-27 of Rho-subfamily GTPases on glucosylation by the large clostridial cytotoxins TcsL-1522, TcdB-1470 and TcdB-8864

1999

Here we report data describing some principles of the interaction between small GTP-binding proteins and large Clostridial cytotoxins (LCTs). Our investigation was based on the differential glucosylation of Rac1 versus RhoA by LCTs TcsL-1522, TcdB-1470 and TcdB-8864. Chimeric RhoA/Rac1 proteins and GTPases mutated at defined regions or single amino acids were used as substrates. Starting with chimeric Rac/Rho proteins we demonstrated that proteins containing the N-terminal 73 amino acids of Rac1 (but not those of RhoA) were efficiently glucosylated. Within this stretch, three regions differ significantly in Rac1 and RhoA. Regions containing amino acids 41-45 and 50-54 had no effect on toxin…

chemistry.chemical_classificationRHOAGlycosylationbiologyRAC1GTPaseBiochemistryAmino acidchemistry.chemical_compoundBiochemistrychemistryCdc42 GTP-Binding Proteinbiology.proteinBinding sitePeptide sequenceEuropean Journal of Biochemistry
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Dehydroepiandrosterone Induction of the Abcd2 and Abcd3 Genes encoding peroxisomal ABC Transporters

2003

Dehydroepiandrosterone (DHEA) is a peroxisome proliferator known to increase the expression of the genes encoding the peroxisomal s-oxidation enzymes in rodents. Using RT-PCR, we analysed the expression of the Abcd2 and Abcd3 genes encoding the peroxisomal ABC transporters ALDRP (ALD related protein) and PMP70 (70 kDa peroxisomal membrane protein) in primary cultures of rats hepatocytes treated with sulfated DHEA. We observed a time (12-72h) and dose (125-500μM) dependent increase in the expression of both genes.

chemistry.chemical_classificationSulfationEnzymeBiochemistrybiologychemistryABCD3ABCD2biology.proteinDehydroepiandrosteroneATP-binding cassette transporterPeroxisomeGene
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Tuning antiviral CD8 T-cell response via proline-altered peptide ligand vaccination

2019

AbstractViral escape from CD8+cytotoxic T lymphocyte responses correlates with disease progression and represents a significant challenge for vaccination. Here, we demonstrate that CD8+T cell recognition of the naturally occurring MHC-I-restricted LCMV-associated immune escape variant Y4F is restored following vaccination with a proline-altered peptide ligand (APL). The APL increases MHC/peptide (pMHC) complex stability, rigidifies the peptide and facilitates T cell receptor (TCR) recognition through reduced entropy costs. Structural analyses of pMHC complexes before and after TCR binding, combined with biophysical analyses, revealed that although the TCR binds similarly to all complexes, t…

chemistry.chemical_classificationbiologyT cellT-cell receptorPeptidechemical and pharmacologic phenomenaMajor histocompatibility complexCell biologyVaccinationmedicine.anatomical_structurechemistrymedicinebiology.proteinCytotoxic T cellAlleleCD8
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