Search results for "binding"

showing 10 items of 3896 documents

Bimodal Effect of Amphiphilic Biocide Concentrations on Fluidity of Lipid Membranes

1996

Abstract Using the spin label method (ESR) it has been shown that biologically active, amphiphilic compounds (quaternary ammonium salts -AS) containing polar heads with single and double positive charge caused, at low concentrations, decrease fluidity of liposome membranes formed with egg yolk lecithin (EYL). At higher concentrations an increase in fluidity was observed. With compounds having a single positive charge minimum fluidity of membrane structure occurs in the range of 1 to 3%, with compounds containing double positive charge -in the range of 4 -6 % . That effect does not depend on polar head size and length of alkyl chains of the AS used. Analysis of the electrostatic interaction …

chemistry.chemical_classificationLiposomefood.ingredientMembrane FluidityBinding energyInorganic chemistryElectron Spin Resonance SpectroscopyEgg YolkModels BiologicalLecithinGeneral Biochemistry Genetics and Molecular BiologyDivalentCyclic N-OxidesQuaternary Ammonium CompoundsMembranefoodchemistryBiochemistryLiposomesPhosphatidylcholinesMembrane fluiditySpin LabelsUltrasonicsSpin labelAlkylZeitschrift für Naturforschung C
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De-epoxidation of Violaxanthin after Reconstitution into Different Carotenoid Binding Sites of Light-harvesting Complex II

2001

In higher plants, the de-epoxidation of violaxanthin (Vx) to antheraxanthin and zeaxanthin is required for the pH-dependent dissipation of excess light energy as heat and by that process plays an important role in the protection against photo-oxidative damage. The de-epoxidation reaction was investigated in an in vitro system using reconstituted light-harvesting complex II (LHCII) and a thylakoid raw extract enriched in the enzyme Vx de-epoxidase. Reconstitution of LHCII with varying carotenoids was performed to replace lutein and/or neoxanthin, which are bound to the native complex, by Vx. Recombinant LHCII containing either 2 lutein and 1 Vx or 1.6 Vx and 1.1 neoxanthin or 2.8 Vx per mono…

chemistry.chemical_classificationLuteinBinding SitesAntheraxanthinPhotosynthetic Reaction Center Complex Proteinsfood and beveragesCell BiologyXanthophyllsbeta CaroteneBiochemistryZeaxanthinKineticschemistry.chemical_compoundchemistryNeoxanthinBiochemistryThylakoidXanthophyllBiophysicsEpoxy CompoundsMolecular BiologyCarotenoidViolaxanthinJournal of Biological Chemistry
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The Binding of Xanthophylls to the Bulk Light-harvesting Complex of Photosystem II of Higher Plants

2002

The pigment composition of the light-harvesting complexes (LHCs) of higher plants is highly conserved. The bulk complex (LHCIIb) binds three xanthophyll molecules in combination with chlorophyll (Chl) a and b. The structural requirements for binding xanthophylls to LHCIIb have been examined using an in vitro reconstitution procedure. Reassembly of the monomeric recombinant LHCIIb was performed using a wide range of native and nonnative xanthophylls, and a specific requirement for the presence of a hydroxy group at C-3 on a single β-end group was identified. The presence of additional substituents (e.g.at C-4) did not interfere with xanthophyll binding, but they could not, on their own, supp…

chemistry.chemical_classificationLuteinPhotosystem IIfood and beveragesCell BiologyBiologyXanthophyll bindingBiochemistryeye diseasesZeaxanthinLight-harvesting complexchemistry.chemical_compoundchemistryBiochemistryXanthophyllMolecular BiologyCarotenoidViolaxanthinJournal of Biological Chemistry
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Assembly of the Major Light-harvesting Chlorophyll-a/b Complex

2006

The major light-harvesting chlorophyll-a/b complex in most higher plants contains three carotenoids, lutein, neoxanthin, and violaxanthin. How these pigments are assembled into the complex during its biogenesis is largely unknown. Here we show that neoxanthin but not lutein can dissociate from the fully assembled complex. Its equilibrium binding constant in a detergent system (0.1% n-dodecyl-beta-D-maltoside) was determined to be > or = 10(6) m(-1). Neoxanthin insertion into light-harvesting chlorophyll-a/b complex prefolded from overexpressed apoprotein (Lhcb1*2 from Pisum sativum) in the presence of chlorophylls a, b, and lutein as the sole carotenoid is kinetically controlled by an activ…

chemistry.chemical_classificationLuteinfood and beveragesCell BiologyPhotochemistryPhotosynthesisBiochemistryBinding constantDissociation (chemistry)B vitaminschemistry.chemical_compoundchemistryNeoxanthinMolecular BiologyCarotenoidViolaxanthinJournal of Biological Chemistry
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Analysis of Subcellular Components by Fluorescent-Lectin Binding and Flow Cytometry

2003

Because of their extensive availability and the wide spectrum of carbohydrates that may be specifically bound, lectins have become essential reagents for detection and quantitation of glycoconjugates in solution and in cell surfaces, identification and separation of cells, and functional studies based on membrane properties (1,2).

chemistry.chemical_classificationMembranechemistryBiochemistrymedicine.diagnostic_testGlycoconjugateLectin bindingmedicineFunctional studiesFluorescenceFlow cytometry
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Two penta­de­hydro­peptides with different configurations of the ΔPhe residues

2009

Comparison of the crystal structures of two pentadehydropeptides containing DeltaPhe residues, namely (Z,Z)-N-(tert-butoxycarbonyl)glycyl-alpha,beta-phenylalanylglycyl-alpha,beta-phenylalanylglycine (or Boc(0)-Gly(1)-Delta(Z)Phe(2)-Gly(3)-Delta(Z)Phe(4)-Gly(5)-OH) methanol solvate, C(29)H(33)N(5)O(8) x CH(4)O, (I), and (E,E)-N-(tert-butoxycarbonyl)glycyl-alpha,beta-phenylalanylglycyl-alpha,beta-phenylalanylglycine (or Boc(0)-Gly(1)-Delta(E)Phe(2)-Gly(3)-Delta(E)Phe(4)-Gly(5)-OH), C(29)H(33)N(5)O(8), (II), indicates that the Delta(Z)Phe residue is a more effective inducer of folded structures than the Delta(E)Phe residue. The values of the torsion angles phi and psi show the presence of two …

chemistry.chemical_classificationMolecular StructureProtein ConformationOrganic CompoundsStereochemistryHydrogen bondPhenylalanineMolecular Sequence DataHydrogen BondingPhenylalanineGeneral MedicineCrystal structureCrystallography X-RayGeneral Biochemistry Genetics and Molecular BiologyAmino acidCrystallographyResidue (chemistry)Protein structurechemistryIntramolecular forceMoleculeAmino Acid SequenceOligopeptidesProtein BindingActa Crystallographica Section C-Crystal Structure Communications
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Photoaffinity cross-linking of F1ATPase from the thermophilic bacterium PS3 by 3′-arylazido-β-alanyl-2-azido ATP

1989

AbstractThe photoactivatable bifunctional 3′-arylazido-β-alanyl-2-azido ATP (2,3′-DiN3ATP) has been applied to study the localization of the nucleotide-binding sites of coupling factor 1 (F1ATPase, TF1) from the thermophilic bacterium PS3 by photoaffinity cross-linking. UV irradiation of TF1 in the presence of 2,3′-DiN3ATP results in the nucleotide-dependent formation of various higher molecular mass cross-links formed by two, three or even four α- and/or β-subunits. The differences observed upon photoaffinity cross-linking by the bifunctional 2-azido ATP or 8-azido ATP analog are discussed. They are probably due to the varied maximal distance between both azido groups, or to the different …

chemistry.chemical_classificationMolecular massbiologyStereochemistryProtein subunitNucleotide conformationBiophysicsCell Biologybiology.organism_classificationBiochemistrychemistry.chemical_compoundEnzymechemistryStructural BiologyGeneticsPhotoaffinity crosslinkingATPase F1-NucleotideNucleotide-binding siteBinding siteBifunctionalInterfacial localizationMolecular BiologyThermophilic bacterium PS3BacteriaFEBS Letters
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Indanedione based binary chromophore supramolecular systems as a NLO active polymer composites

2010

Novel route to obtain EO material is proposed by supramolecular assembly of neutral-ground-state (NGS) and zwitterionic (ZWI) NLO chromophores in binary chromophore organic glass (BCOG) host–guest system. On a basis of our Langeven Dynamics (LD) molecular modeling combined with quantum chemical calculations, we have shown that anticipated enhancement NLO efficiency of BCOG material is possible via electrostatic supramolecular assembly of NGS with ZWI chromophore in antiparallel manner. Binding energy of such complex could be more dependent on molecular compatibility of components and local (atomic) charge distribution, then overall molecular dipole moments. According to our LD simulations t…

chemistry.chemical_classificationMolecular modelStereochemistryOrganic ChemistryBinding energySupramolecular chemistryPolymerChromophorePhotochemistryAtomic and Molecular Physics and OpticsElectronic Optical and Magnetic MaterialsSupramolecular assemblyInorganic Chemistrychemistry.chemical_compoundDipolechemistryPyridiniumElectrical and Electronic EngineeringPhysical and Theoretical ChemistrySpectroscopyOptical Materials
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Functional analysis of the cysteine residues and the repetitive sequence ofSaccharomyces cerevisiaePir4/Cis3: the repetitive sequence is needed for b…

2003

Identification of PIR/CIS3 gene was carried out by amino-terminal sequencing of a protein band released by β-mercaptoethanol (β-ME) from S. cerevisiae mnn9 cell walls. The protein was released also by digestion with β-1,3-glucanases (laminarinase or zymolyase) or by mild alkaline solutions. Deletion of the two carboxyterminal Cys residues (Cys214-12aa-Cys227-COOH), reduced but did not eliminate incorporation of Pir4 (protein with internal repeats) by disulphide bridges. Similarly, site-directed mutation of two other cysteine amino acids (Cys130Ser or Cys197Ser) failed to block incorporation of Pir4; the second mutation produced the appearance of Kex2-unprocessed Pir4. Therefore, it seems th…

chemistry.chemical_classificationMutationSaccharomyces cerevisiaeBioengineeringBiologymedicine.disease_causebiology.organism_classificationApplied Microbiology and BiotechnologyBiochemistryMolecular biologyAmino acidCell wallBiochemistrychemistryGeneticsmedicineSecretionGeneBiotechnologyCysteineBinding domainYeast
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Photoinduced and Self‐Activated Nuclease Activity of Copper(II) Complexes with N ‐(Quinolin‐8‐yl)quin­olin‐8‐sulfonamide – DNA and Bovine Serum Album…

2016

Two CuII complexes with a new quinoline sulfonamide derivative and phenanthroline (phen), [Cu(QSQ)(phen)]ClO4·0.5H2O (1) and [Cu(QSQ)(phen)(H2O)]ClO4 (2) [HQSQ = N-(quinolin-8-yl)quinolin-8-sulfonamide], have been synthesized and physicochemically characterized. Single-crystal X-ray diffraction studies have revealed a highly distorted trigonal-bipyramidal structure for 1 (τ = 0.68) and an almost perfect trigonal-bipyramidal geometry for 2 (τ = 0.92). DNA binding studies, which were performed by thermal denaturation, viscometry, fluorescence spectroscopy, and cyclic voltammetry, indicated a partial intercalation of 1 with Kapp = 2.45 × 106 M–1. The nuclease activity of 1 was investigated upo…

chemistry.chemical_classificationNucleasebiology010405 organic chemistryStereochemistryPhenanthrolineQuinolineIntercalation (chemistry)Plasma protein binding010402 general chemistry01 natural sciencesMedicinal chemistry0104 chemical sciencesSulfonamideInorganic Chemistrychemistry.chemical_compoundchemistrybiology.proteinBovine serum albuminDNAEuropean Journal of Inorganic Chemistry
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