Search results for "Bioinorganic Chemistry"

showing 10 items of 30 documents

Studio dell'interazione di DNA con complessi di metalli di transizione

2014

G-quadruplextransition metal complexUv-ViDNACircular dichroismdicroismo circolareInorganic Chemistrymetal complexSchiff basechimica bioinorganicaintercalantiG4complessi metalliciChimica inorganicaSettore CHIM/03 - Chimica Generale E Inorganicametalli di transizioneBasi di SchiffG4-stabilizerBioinorganic Chemistryintercalator
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Crystalline nanorods as possible templates for the synthesis of amorphous biosilica during spicule formation in Demospongiae.

2009

In tandem: High-resolution TEM shows that during the initial stages of demosponge spicule formation, a primordial crystalline structure is formed within the axial filament. The recently developed electron diffraction tomography technique (ADT) reveals that the nanorods have a layered structure that matches smectitic phyllosilicates. These intracellular nanorods have been considered as precursors of mature spicules. High-resolution microscopy shows that, during the initial stages of demosponge spicule formation, a primordial crystalline structure is formed within the axial filament. The recently developed electron diffraction tomography technique reveals that the nanorods have a layered stru…

SpiculeMaterials scienceElectronsCrystal structureBiochemistrybioinorganic chemistryDemospongeSponge spiculeMicroscopy Electron TransmissionX-Ray DiffractionnanostructuresAnimalsMolecular BiologyNanotubesbiologyElectron crystallographysilicateinOrganic Chemistrybioinorganic chemistry; electron crystallography; nanostructures; silicatein; spiculesbiology.organism_classificationSilicon DioxidespiculesAmorphous solidPoriferaCrystallographyelectron crystallographyElectron diffractionMicroscopy Electron ScanningMolecular MedicineNanorodChembiochem : a European journal of chemical biology
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Silicateins - A Novel Paradigm in Bioinorganic Chemistry: Enzymatic Synthesis of Inorganic Polymeric Silica

2013

The inorganic matrix of the siliceous skeletal elements of sponges, that is, spicules, is formed of amorphous biosilica. Until a decade ago, it remained unclear how the hard biosilica monoliths of the spicules are formed in sponges that live in a silica-poor (<50 mu m) aquatic environment. The following two discoveries caused a paradigm shift and allowed an elucidation of the processes underlying spicule formation; first the discovery that in the spicules only one major protein, silicatein, exists and second, that this protein displays a bio-catalytical, enzymatic function. These findings caused a paradigm shift, since silicatein is the first enzyme that catalyzes the formation of an inorga…

SpiculeNew horizonsPolymersNanotechnology02 engineering and technologyCatalysisCalcium Carbonate03 medical and health sciencesSponge spiculeAnimals030304 developmental biology0303 health sciencesInorganic polymerChemistrySilicatesOrganic ChemistrySubstrate (chemistry)Bioinorganic chemistryGeneral ChemistryEnzymatic synthesisSilicon Dioxide021001 nanoscience & nanotechnologyCathepsinsPoriferaChemistry BioinorganicChemical engineeringBiocatalysisInorganic matrixSuberites0210 nano-technology
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Sometimes less is more—the impact of the number of His residues on the stability of Zn(ii)–SmtB and BigR4 α-5 domain complexes

2021

The increasing number of antibiotic-resistant pathogens has become one of the major health problems of modern times, including infections caused by Mycobacterium tuberculosis. One of the possible mammalian immune system responses to mycobacterial infection is the increase of the zinc(II) concentration in phagosomes to a toxic level. The mycobacterial SmtB protein belongs to the family of ArsR/SmtB transcription regulators. In the presence of high concentrations of metals, SmtB dissociates from DNA and activates the expression of metal efflux proteins. In this work, we focus on the α5 zinc(II) binding domains of SmtB/BigR4 proteins (the latter being the SmtB homolog from non-pathogenic M. sm…

AlanineStereochemistryMutantchemistry.chemical_elementBioinorganic chemistryZincInorganic ChemistryMetalchemistry.chemical_compoundchemistryTranscription (biology)visual_artvisual_art.visual_art_mediumEffluxDNADalton Transactions
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Optical sensing of cyanide using hybrid biomolecular films

2006

The selective sensing of cyanide anions in water has been studied using a hybrid biomaterial composed of a mesoporous TiO2 film of crystalline nanoparticles and the protein hemoglobin. The mesoporous structure of the film prevents protein unfolding and also stabilizes the oxidized form of the prosthetic groups. Low-levels of cyanide anions (<0.2 ppm (0.2 mgr/L)) can be detected by monitoring the changes in the optical properties of the hybrid biomolecular films upon cyanide binding to the heme groups.

biologyCyanideInorganic chemistryBiomaterialNanoparticleBioinorganic chemistryPhotochemistryCofactorInorganic Chemistrychemistry.chemical_compoundchemistryMaterials Chemistrybiology.proteinsense organsHemoglobinPhysical and Theoretical ChemistryMesoporous materialHemeInorganic Chemistry Communications
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Evagination of Cells Controls Bio-Silica Formation and Maturation during Spicule Formation in Sponges

2011

The enzymatic-silicatein mediated formation of the skeletal elements, the spicules of siliceous sponges starts intracellularly and is completed extracellularly. With Suberites domuncula we show that the axial growth of the spicules proceeds in three phases: (I) formation of an axial canal; (II) evagination of a cell process into the axial canal, and (III) assembly of the axial filament composed of silicatein. During these phases the core part of the spicule is synthesized. Silicatein and its substrate silicate are stored in silicasomes, found both inside and outside of the cellular extension within the axial canal, as well as all around the spicule. The membranes of the silicasomes are inte…

SpiculeHistologyMaterials ScienceAquaporinlcsh:MedicineMarine BiologyCytoplasmic GranulesModels BiologicalInorganic ChemistryNatural Materials03 medical and health sciencesSponge spiculeMicroscopy Electron TransmissionAnimal PhysiologyNanotechnologyAnimalslcsh:ScienceBiologyBioinorganic Chemistry030304 developmental biologyNanomaterials0303 health sciencesMultidisciplinarybiologyChemistryVesicleSilicates030302 biochemistry & molecular biologylcsh:RCytoplasmic VesiclesSpectrometry X-Ray EmissionAnatomyMarine TechnologyBiogeochemistrybiology.organism_classificationSilicon DioxideCathepsinsImmunohistochemistrySuberites domunculaChemistryMembraneGeochemistryEvaginationBiophysicslcsh:QSuberitesZoologySuberitesResearch ArticlePLoS ONE
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CH vs. HC—Promiscuous Metal Sponges in Antimicrobial Peptides and Metallophores

2023

Histidine and cysteine residues, with their imidazole and thiol moieties that deprotonate at approximately physiological pH values, are primary binding sites for Zn(II), Ni(II) and Fe(II) ions and are thus ubiquitous both in peptidic metallophores and in antimicrobial peptides that may use nutritional immunity as a way to limit pathogenicity during infection. We focus on metal complex solution equilibria of model sequences encompassing Cys&ndash;His and His&ndash;Cys motifs, showing that the position of histidine and cysteine residues in the sequence has a crucial impact on its coordination properties. CH and HC motifs occur as many as 411 times in the antimicrobial peptide database, while …

metal coordinationOrganic ChemistryPharmaceutical ScienceAnalytical Chemistrybioinorganic chemistryantimicrobial peptidesthermodynamicspotentiometryChemistry (miscellaneous)Drug DiscoveryMolecular Medicinebioinorganic chemistry; antimicrobial peptides; metallophores; thermodynamics; potentiometry; metal coordinationmetallophoresPhysical and Theoretical ChemistryMolecules
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Interaction of Novel Metal Complexes with DNA: Synthetic and Structural Aspects

2009

Metal ions bind to nucleic acids at various positions. This binding can be modulated by using metal complexes with appropriate ligands. Novel mono- and especially dinuclear metal complexes could be a powerful tool to detect rare, but still physiologically relevant, forms of DNA, e.g. the left-handed Z-DNA. In this review, our recent research activities in this area of bioinorganic chemistry are summarized. A special emphasis is laid on the synthetic challenges that arose upon the synthesis of the polyamine ligands. Further, some rather unusual approaches to elucidate the solution structure of copper bound to guanosine monophosphate with the help of pulsed EPR techniques like ENDOR and HYSC…

10120 Department of ChemistryMono- and dinuclear metal complexesMetal ions in aqueous solutionand dinuclear metal complexes1600 General ChemistrydnaBioinorganic chemistryZ-DNAMetalchemistry.chemical_compoundMono- and Dinuclear Metal ComplexeGuanosine monophosphate540 ChemistryQD1-999Pulsed EPRCrystal structureBioinorganic chemistryGeneral MedicineGeneral ChemistryZ-DNACombinatorial chemistrySettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)Chemistrychemistryvisual_artCrystal structuresNucleic acidvisual_art.visual_art_mediumMonoSynthetic ChemistryDNAZ
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Biomimetic Mn-catalases based on dimeric manganese complexes in mesoporous silica for potential antioxidant agent

2015

Two new structural and functional models of the Mn-catalase with formula [{Mn(III)(bpy)(H2O)}(μ-2-MeOC6H4CO2)2(μ-O){Mn(III)(bpy)(X)}]X, where X = NO3 (1) and ClO4 (2) and bpy = 2,2'-bipyridine, were synthesized and characterized by X-ray diffraction. In both cases, a water molecule and an X ion occupy the monodentate positions. The magnetic properties of these compounds reveal a weak antiferromagnetic behavior (2J = -2.2 cm(-1) for 1 and -0.7 cm(-1) for 2, using the spin Hamiltonian H = -2J S1·S2) and negative zero-field splitting parameter DMn (-4.6 cm(-1) and -3.0 cm(-1) for 1 and 2, respectively). This fact, together with the nearly orthogonal orientation of the Jahn-Teller axes of the M…

DenticitySilicon dioxideInorganic chemistrychemistry.chemical_elementManganeseCrystallography X-Ray010402 general chemistryLigands01 natural sciencesAntioxidantsCoordination complexBioinorganic chemistryInorganic ChemistryBipyridinechemistry.chemical_compoundBiomimeticsMoleculeManganèsPhysical and Theoretical ChemistryMaterialsComputingMilieux_MISCELLANEOUSchemistry.chemical_classificationManganese010405 organic chemistryPhotoelectron SpectroscopyMesoporous silicaQuímica bioinorgànicaCatalaseSilicon Dioxide0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryCrystallographyLligandschemistryHybrid materialDimerization
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Zn(II)-alloferon complexes - Similar sequence, different coordination modes, no antibacterial activity.

2020

Often, in the search for a highly defined scientific phenomenon, a different one becomes apparent. This was also the case of this work, in the scope of which we planned to search for metal-enhanced, novel antibacterial/ antifungal compounds. Instead, we denied the existence of such and revealed the details of the bioinorganic chemistry of Zn(II)-alloferon complexes. Zinc(II) complexes of alloferon 1 and 2, ligands with a sequential difference of one amino acid only, show a substantially different coordination pattern at physiological pH. In the case of Zn(II)-alloferon 1 species, a histamine-like binding mode is observed (N-terminal amine and imidazole of His-1) and the coordination sphere …

Coordination sphereAlloferon; Metal-antimicrobial peptide complex; Metal-peptide thermodynamics; Zinc(II)StereochemistryProton Magnetic Resonance Spectroscopychemistry.chemical_elementZincMicrobial Sensitivity Tests010402 general chemistryLigands01 natural sciencesBiochemistryMass SpectrometryInorganic ChemistryAlloferonchemistry.chemical_compoundStructure-Activity RelationshipCoordination ComplexesImidazoleMetal-antimicrobial peptide complexHistidineAmino Acid Sequencechemistry.chemical_classificationMetal-peptide thermodynamics010405 organic chemistryBioinorganic chemistryZinc(II)0104 chemical sciencesAmino acidAnti-Bacterial AgentsZincchemistryThermodynamicsChemical stabilityAmine gas treatingAntibacterial activityPeptidesJournal of inorganic biochemistry
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