Understanding the mechanism by which Gd(III) coiled coils achieve magnetic resonance relaxivity - a study into the water coordination chemistry.

A class of Gd(III) coiled coils achieve high MRI relaxivity, in part due to their slow rotational correlation time. However, extending their length is unable to further enhance performance, as the mechanism by which relaxivity is achieved is dominated by the presence of three inner sphere waters in rapid exchange, through an associative mechanism.

Solution behavior of iron(III) and iron(II) porphyrins in DMSO and reaction with superoxide. Effect of neighboring positive charge on thermodynamics, kinetics and nature of iron-(su)peroxo product.

The solution behavior of iron(III) and iron(II) complexes of 5(4),10(4),15(4),20(4)-tetra-tert-butyl-5,10,15,20-tetraphenylporphyrin (H(2)tBuTPP) and the reaction with superoxide (KO(2)) in DMSO have been studied in detail. Applying temperature and pressure dependent NMR studies, the thermodynamics of the low-spin/high-spin equilibrium between bis- and mono-DMSO Fe(II) forms have been quantified (K(DMSO) = 0.082 ± 0.002 at 298.2 K, ΔH° = +36 ± 1 kJ mol(-1), ΔS° = +101 ± 4 J K(-1) mol(-1), ΔV° = +16 ± 2 cm(3) mol(-1)). This is a key activation step for substitution and inner-sphere electron transfer. The superoxide binding constant to the iron(II) form of the studied porphyrin complex was found to be (9 ± 0.5) × 10(3) M(-1), and does not change significantly in the presence of the externally added crown ether in DMSO (11 ± 4) × 10(3) M(-1). The rate constants for the superoxide binding (k(on) = (1.30 ± 0.01) × 10(5) M(-1) s(-1)) and release (k(off) = 11.6 ± 0.7 s(-1)) are not affected by the presence of the external crown ether in solution. The resulting iron(II)-superoxide adduct has been characterized (mass spectrometry, EPR, high-pressure UV/Vis spectroscopy) and upon controlled addition of a proton source it regenerates the starting iron(II) complex. Based on DFT calculations, the reaction product without neighboring positive charge has iron(II)-superoxo character in both high-spin side-on and low-spin end-on forms. The results are compared to those obtained for the analogous complex with covalently attached crown ether, and more general conclusions regarding the spin-state equilibrium of iron(II) porphyrins, their reaction with superoxide and the electronic structure of the product species are drawn.

Heat shock induces the synthesis of the inflammatory mediator leukotriene B4 in human pulp cells.

AIM: To measure the synthesis of leukotriene B4 (LTB4) in cultures of human dental pulp cells induced by heat shock. METHODOLOGY: Primary pulp cells (PC) and dental pulp stem cells (DPSC) were cultivated under appropriate conditions. For the characterization of PC the expression of dentine sialophosphoprotein (DSPP) was evaluated by reverse transcription-polymerase chain reaction. Thermal stimulation of cell cultures was performed at temperatures of 37, 38, 39, 40, 42 and 45 degrees C for stimulation times of 5 and 30 s. LTB4 was quantified by reversed-phase high-performance chromatography and differences between the LTB4 concentrations of controls and heat stimulated cells were analysed with Friedman analysis of variances by ranks and multiple comparisons (P < 0.05). RESULTS: Both cell cultures expressed DSPP under the conditions of the present experiment. The analysis revealed significantly enhanced LTB4 synthesis following thermal stimulations at 38, 39, 40, 42 and 45 degrees C compared with unstimulated controls for both PC and DPSC. CONCLUSION: The present study demonstrated the capability of pulp cells to synthesize the arachidonic acid mediator LTB4 in response to heat shock. LTB4 has the capacity to induce inflammatory reactions and to sensitise afferent nociceptive nerve endings. LTB4 synthesis is induced by minor temperature changes, which are relevant for various clinical situations.

Kinetics and mechanism of the reversible binding of nitric oxide to reduced cobalamin B(12r) (Cob(II)alamin).

The reduced form of aquacobalamin binds nitric oxide very effectively to yield a nitrosyl adduct, Cbl(II)-NO. UV-vis, (1)H-, (31)P-, and (15)N NMR data suggest that the reaction product under physiological conditions is a six-coordinate, "base-on" form of the vitamin with a weakly bound alpha-dimethylbenzimidazole base and a bent nitrosyl coordinated to cobalt at the beta-site of the corrin ring. The nitrosyl adduct can formally be described as Cbl(III)-NO-. The kinetics of the binding and dissociation reactions was investigated by laser flash photolysis and stopped-flow techniques, respectively. The activation parameters, DeltaH, DeltaS, and DeltaV, for the forward and reverse reactions were estimated from the effect of temperature and pressure on the kinetics of these reactions. For the "on" reaction of Cbl(II) with NO, the small positive DeltaS and DeltaV values suggest the operation of a dissociative interchange (I(d)) substitution mechanism at the Co(II) center. Detailed laser flash photolysis and (17)O NMR studies provide evidence for the formation of water-bound intermediates in the laser flash experiments and strongly support the proposed I(d) mechanism. The kinetics of the "off" reaction was studied using an NO-trapping technique. The respective activation parameters are also consistent with a dissociative interchange mechanism.

Influence of chelate effects on the water-exchange mechanism of polyaminecarboxylate complexes of iron(III).

The effect of temperature and pressure on the water-exchange reactions of complexes of the type [FeIII(L)(H2O)x]n-, where L = edta4- (ethylenediaminetetraacetate), Hedta3- (monoprotonated form of edta), cdta4- (trans-1,2-diaminocyclohexanetetraacetate), edds4- (s,s-ethylenediaminedisuccinate), 1,3-pdta4- (1,3-propylenediaminetetraacetate), and alpha,beta-eddadp4-(alpha,beta-ethylenediaminediaceatedipropionate), was studied by employing 17O NMR techniques. The effect of potentially hexadentate ligands, covering a systematic variation of the size, substituents, and overall coordination geometry, on iron(III) complexes was investigated in terms of the lability of the coordinated water and the underlying exchange mechanism. For most of the systems studied, the results are in agreement with a dissociatively activated water-exchange mechanism for the seven-coordinate complexes. The absolute magnitudes of the volumes of activation are small and fit an I(d) mechanism. The results contribute to a better understanding of the nature, reactivity, and substitution mechanism of the selected complexes in solution.

The reactivity of N-coordinated amides in metallopeptide frameworks: molecular events in metal-induced pathogenic pathways?

The amino acid derived tertiary amide ligand tert-butoxycarbonyl-(S)-alanine-N,N-bis(picolyl)amide (Boc-(S)-Ala-bpa, 1) has been synthesized as a model for metal-coordinating peptide frameworks. Its reactions with copper(II) and cadmium(II) salts have been studied. Binding of Cu2+ results in amide bond cleavage and formation of [(bpa)(solvent)Cu]2+ complexes. In contrast, the stable, eight-coordinate complex [(Boc-(S)-Ala-bpa)Cd(NO3)2] (5) has been isolated and characterized by X-ray crystallography. An unusual tertiary amide nitrogen coordination is observed in 5; this gives rise to significantly reduced cis-trans isomerization barriers. Possible implications for metal-induced conformational changes in proteins are discussed.