RESUMEN
The reaction of hydroxyl radicals ((â¢)OH) with Aß1-16 peptide was carried out using pulse radiolysis to understand the effect of oxidation of peptide on its copper-binding properties. This reaction produced oxidized, dimeric and trimeric Aß1-16 peptide species. The formation of these products was established with the help of fluorescence spectroscopy and mass spectrometry. The mass spectral data indicate that the major site of oxidation is at His6, while the site for dimerization is at Tyr10. Diethyl pyrocarbonate-treated Aß1-16 peptide did not produce any trimeric species upon oxidation with (â¢)OH. The quantitative chemical modification studies indicated that one of the three histidine residues is covalently modified during pulse radiolysis. The copper-binding studies of the oxidized peptide revealed that it has similar copper-binding properties as the unoxidized peptide. Further, the cytotoxicity studies point out that both oxidized and unoxidized Aß1-16 peptide are equally efficient in producing free radicals in presence of copper and ascorbate that resulted in comparable cell death.
Asunto(s)
Péptidos beta-Amiloides/química , Cobre/química , Fragmentos de Péptidos/química , Secuencia de Aminoácidos , Péptidos beta-Amiloides/metabolismo , Péptidos beta-Amiloides/toxicidad , Línea Celular Tumoral , Cobre/metabolismo , Humanos , Radical Hidroxilo/química , Radical Hidroxilo/metabolismo , Datos de Secuencia Molecular , Oxidación-Reducción , Fragmentos de Péptidos/metabolismo , Fragmentos de Péptidos/toxicidad , Radiólisis de Impulso/métodos , Espectrometría de Fluorescencia , Espectrometría de Masa por Láser de Matriz Asistida de Ionización DesorciónRESUMEN
A series of metal complexes having the general formula [Ru(bpy)(n)(mebpq(+))(3-n)]((5-n)+) (n = 0, 1,2,3)(2,2'-bipyridine (bpy) and/or 2-(N-methylpyridyl)3-pyridyl quinoxaline (mebpq(+)) were synthesized and characterized by optical, elemental analysis, NMR and electrochemical methods. The absorption spectra of complexes have bands in the UV region (< or = 350 nm) consisting of an intense pi --> pi* transition due to the ligands (epsilon approximately 10(5) dm(3) mol(-1) cm(-1)) and in the visible region dominated by MLCT (dpi --> pi*). The emission intensity is the least when ruthenium is fully coordinated to mebpq(+) and it increased 50 fold on going to [Ru(bpy)(3)]Cl(2). Electrochemical data revealed that the Ru(II)/Ru(III) oxidation peaks are in the range 1.31 to 1.76 V and the sequential replacement of bpy by mebpq(+) resulted in the increase of the oxidation potential. The reactions of oxidizing and reducing radicals (OH, O(-), N(3) , Cl(2)(-) and e) with these complexes were studied by pulse radiolysis. The OH radical reacts with all complexes at diffusion controlled rates and the k values increased from 6.2 to 9.8 x 10(9) dm(3) mol(-1) s(-1) on going from [Ru(bpy)(3)]Cl(2) to [Ru(mebpq(+))(3)](PF(6))(5). The rates of reaction of e with Ru(II) complexes are high (k approximately 10(10) dm(3) mol(-1) s(-1)) and the reaction leads to the formation of the radical anion of the bipyridine in [Ru(bpy)(3)]Cl(2) and tertiary quinoxaline radical in mixed complexes containing mebpq(+). The underlying reaction mechanism is discussed.
Asunto(s)
Compuestos Organometálicos/química , Compuestos Organometálicos/síntesis química , Piridinas/química , Quinoxalinas/química , Rutenio/química , Estructura Molecular , Oxidación-ReducciónRESUMEN
The construction of two-dimensional (2D) copper halide networks within a variety of perovskite hosts by a low-temperature topochemical method is demonstrated. Ion exchange between some layered perovskite oxides of the type A'[An - 1(M,M')nO3n + 1] (A' = alkali metal, H, NH4; A = alkaline earth, rare earth, or Bi; M,M' = Nb, Ta, Ti; n = 2, 3) with CuX2 (X = Cl, Br) results in the oxyhalides (CuX)[An - 1(M,M')nO3n + 1]. Rietveld refinements from X-ray powder diffraction data show that the structures of these new copper oxyhalides contain edge-sharing CuO2X4 octahedra sandwiched between the M/M'O6 octahedra of the perovskite slabs. The compounds are low-temperature phases that decompose well below 700 degrees C. The copper oxyhalides exhibit antiferromagnetic ordering resulting from the magnetic exchange interactions within the planar Cu-X networks.
RESUMEN
The modulation of radiation induced lipid peroxidation in synaptosomes by iron (II) and iron (III) complexes of two naturally occurring and therapeutically relevant naphthoquinones viz. 5,hydroxy-1,4 naphthoquinone; juglone and 2,hydroxy-1,4 naphthoquinone; lawsone, have been studied. At lower concentrations the complexes enhance lipid peroxidation predominantly through redox cycling as observed for Fe(II)- juglonate while at higher concentrations the complexes tend to limit lipid peroxidation through fast recombinations.
RESUMEN
Copper(II) complexes of the type [Cu(L)X], where L = tridentate anion of 2-acetylpyridine N4-diethyl thiosemicarbazone and X = C1 or Br, were screened against seven fungal strains pathogenic to man viz. Aspergillus niger, Aspergillus fumigatus, Candida albicans, Cryptococcus neoformans, Tricophyton rubrum, Epidermophyton floccosum and Microsporum canis. The greater growth inhibition exhibited by the bromo complex can be explained on the basis of its lower Cu(II)/Cu(I) redox couple and greater covalent bonding. These compounds represent a novel class of metal-based antifungal agents which provide opportunities for a large number of synthetic variations for modulation of the activities.