Reactive oxygen and nitrogen species function in host defense via mechanisms that remain controversial. Pathogens might encounter varying levels of these species, but bulk measurements cannot resolve such heterogeneity. We used single-cell approaches to determine the impact of oxidative and nitrosative stresses on individual Salmonella during early infection in mouse spleen. Salmonella encounter and respond to both stresses, but the levels and impact vary widely. Neutrophils and inflammatory monocytes kill Salmonella by generating overwhelming oxidative stress through NADPH oxidase and myeloperoxidase. This controls Salmonella within inflammatory lesions but does not prevent their spread to more permissive resident red pulp macrophages, which generate only sublethal oxidative bursts. Regional host expression of inducible nitric oxide synthase exposes some Salmonella to nitrosative stress, triggering effective local Salmonella detoxification through nitric oxide denitrosylase. Thus, reactive oxygen and nitrogen species influence dramatically different outcomes of disparate Salmonella-host cell encounters, which together determine overall disease progression.

We designed and tested an antioxidant nanoreactor based on encapsulation of Cu,Zn superoxide dismutase in amphiphilic copolymer nanovesicles, the membranes of which are oxygen permeable. The nanovesicles, made of poly(2-methyloxazoline)-poly(dimethylsiloxane)-poly(2-methyloxazoline), successfully encapsulated the protein during their self-assembling process, as proved by confocal laser-scanning microscopy and fluorescence-correlation spectroscopy. Electron paramagnetic resonance spectroscopy and circular dichroism analyses showed that no structural changes appeared in the protein molecules once inside the inner space of the nanovesicles. The function of this antioxidant nanoreactor was tested by pulse radiolysis, which demonstrated that superoxide dismutase remains active inside the nanovesicles and detoxifies the superoxide radical in situ. The membrane of our triblock copolymer nanovesicles plays a double role, both to shield the sensitive protein and to selectively let superoxide and dioxygen penetrate to its inner space. This simple and robust hybrid system provides a selective shielding of sensitive enzymes from proteolytic attack and therefore a new direction for developing drug delivery applications.

The self-assembly of double-hydrophilic poly(ethylene oxide)–poly(2-methyl-2-oxazoline) diblock copolymers in water has been studied. Isothermal titration calorimetry, small-angle X-ray scattering, and analytical ultracentrifugation suggest that only single polymer chains are present in solution. In contrast, light scattering and transmission electron microscopy detect aggregates with radii of ca. 100 nm. Pulsed field gradient NMR spectroscopy confirms the presence of aggregates, although only 2% of the polymer chains undergo aggregation. Water uptake experiments indicate differences in the hydrophilicity of the two blocks, which is believed to be the origin of the unexpected aggregation behavior (in accordance with an earlier study by Ke et al. [Macromolecules 2009, 42, 5339–5344]). The data therefore suggest that even in double-hydrophilic block copolymers, differences in hydrophilicity are sufficient to drive polymer aggregation, a phenomenon that has largely been overlooked or ignored so far.

Amphiphilic poly(acrylic acid)-block-poly(n-butylacrylate) block copolymer films at the air-water interface have been mineralized with calcium phosphate. The polymers form stable monolayers at the free surface. Their stability is virtually independent of ion strength or pH changes in the subphase. The outcome of calcium phosphate crystallization depends on the calcium and phosphate concentrations, the stirring rate of the subphase, and the subphase pH. At low calcium and phosphate concentrations (2 mM), uniform polymer-calcium phosphate hybrid films form. Higher calcium and phosphate concentrations yield less ordered films, which often contain large blocks of material beneath the polymer monolayer. Occasionally, also filaments similar to samples described by Peytcheva et al. (Colloid Polym. Sci., 2002, 280, 218) are observed. Films mineralized at pH values below ca. 6 contain particles that are a few nanometers apart and the resulting films retain some flexibility. Films grown above pH 6 have a higher degree of mineralization. They are stiff and tend to break upon mechanical stress. Overall, the paper illustrates that low calcium phosphate supersaturation in the subphase and a well-defined (but not crystalline) interface are crucial for controlling calcium phosphate mineralization. As a result, the current study could serve as a model for biological mineralization which is more closely related to Nature than films made from e.g. detergents or low molecular mass compounds.

We have recently reported (Taubert, A.; Steiner, P.; Mantion, A. J. Phys. Chem. B 2005, 109, 15542) that DSC traces of an ionic liquid-crystal precursor for CuCl nanoplatelets exhibit an intense exothermic peak. The current paper presents a detailed investigation into the origin of this exothermic peak. Electron paramagnetic resonance spectroscopy, high-temperature X-ray scattering, and isothermal differential scanning calorimetry show that the Cu(II)−Cu(I) reduction is complete after about 35 min. It is the rate-determining step in the CuCl formation process and is responsible for the exothermic peak. Cu(II) reduction strongly overlaps with the formation of a first generation of CuCl particles. The formation of the large CuCl platelets observed in the SEM (Taubert, A. Angew. Chem., Int. Ed., 2004, 43, 5380) is inhibited by the organic matrix and occurs over the course of about 5 h.