Stick-Slip Mechanisms at the Nanoscale

When two surfaces slide past each other, energy is mainly dissipated by stick-slip events. Macroscopic stick-slip is usually explained by asperities that come in and out of contact. Herein, we probe stick-slip at the nanoscale at interfaces and polymer coated interfaces by pulling single polymers covalently attached to an AFM cantilever tip laterally over solid substrates in liquid environment. We find two different stick mechanisms, namely desorption stick (DS) and cooperative stick (CS). While DS-slip resembles the velocity dependence of macroscopic stick-slip, CS-slip shows an increase in friction with velocity. For various reasons we anticipate that both stick mechanisms are necessary for a molecular understanding of stick-slip at the interface and interphase.     

Tailor-made poly(amidoamine)s for controlled complexation and condensation of DNA

A set of polymer carriers for DNA delivery was synthesized by combining monodisperse, sequence-defined poly(amidoamine) (PAA) segments with poly(ethylene oxide) (PEO) blocks. The precise definition of the PAA segments provides the possibility of correlating the chemical structure (monomer sequence) with the resulting biological properties. Three different PAA-PEO conjugates were synthesized by solid-phase supported synthesis, and the cationic nature of the PAA segments was systematically varied. This allows for the tailoring of interactions with double-stranded plasmid DNA (dsDNA). The potential of the PAA-PEO conjugates as non-viral vectors for gene delivery is demonstrated by investigating the dsDNA complexation and condensation properties. Depending on the applied carrier, a transition in polyplex (polymer-DNA ion complex) structures is observed. This reaches from extended ring-like structures to highly compact toroidal structures, where supercoiling of the DNA is induced. An aggregation model is proposed that is based on structural investigations of the polyplexes with atomic force microscopy (AFM) and dynamic light scattering (DLS). While the cationic PAA segment mediates primarily the contact of the carrier to the dsDNA, the PEO block stabilizes the polyplex and generates a "stealth" aggregate, as was suggested by Zeta potentials that were close to zero. The controlled aggregation leads to stable, single-plasmid complexes, and stabilizes the DNA structure itself. This is shown by ethidium bromide intercalation assays and DNase digestion assays. The presented PAA-PEO systems allow for the formation of well-defined single-plasmid polyplexes, preventing hard DNA compression and strongly polydisperse polyplexes. Moreover carrier polymers and the resulting polyplexes exhibit no cytotoxicity, as was shown by viability tests; this makes the carriers potentially suitable for in vivo delivery applications.     

Oscillatory forces of nanoparticle suspensions confined between rough surfaces modified with polyelectrolytes via the layer-by-layer technique

This paper addresses the systematic study of surface roughness effects on the internal structuring of silica nanoparticle suspensions under confinement. The confining surfaces are modified by physisorption of layers of oppositely charged polyelectrolytes with the so-called layer-by-layer technique. The layer-by-layer technique modifies the surface roughness without changing the surface potential of a multilayer with the same outermost layer, by increasing the number of constituent layers and ionic strength of the polyelectrolyte solutions and by selecting an appropriate pair of polyelectrolytes. The oscillatory forces of nanoparticle suspensions with a particle diameter of 26 nm are measured by a colloidal-probe atomic force microscope (CP-AFM). The characteristic lengths of the oscillatory force, i.e., wavelength, which indicates interparticle distance, and decay length, or particle correlation length, are not affected by the surface roughness. The corresponding reduction in the oscillatory amplitude and the shift in the phase correlate with an increase in surface roughness. Increasing surface roughness further induces a disappearance of the oscillations, and both confining surfaces contribute to the effect of surface roughness on the force reduction. In order to show an oscillatory force, the particles have to show positional correlation over a reasonably long range perpendicular to the surface, and the correlation function should be the same over a larger lateral area. This requires that both the particles and the surfaces have a high degree of order or symmetry; otherwise, the oscillation does not occur. A roughness of a few nanometers on a single surface, which corresponds to about 10% of the nanoparticle diameter, is sufficient to eliminate the oscillatory force.     

pH-induced release from P2VP-PEO block copolymer vesicles

The pH-induced release of hydrophilic dyes from poly(2-vinylpyridine-b-ethylene oxide) (P2VP-PEO) block copolymer vesicles is investigated. The structure of the vesicles is characterized using small-angle neutron scattering (SANS) and cryo-electron microscopy (cryo-TEM). A decrease of the pH below 5 leads to protonation and dissolution of the poly-2-vinylpyridine blocks which induces rupture and dissolution of the vesicle membrane. Details of the rupture, dissolution, and release process are studied by fluorescence video microscopy, gel electrophoresis, and high-performance ultrafiltration.     

Role of direct microbial electron transfer in corrosion of steels

It has recently been discovered that many microbial species have the capacity to connect their metabolism to solid electrodes, directly exchanging electrons with them through membrane-bound redox compounds, nevertheless such a direct electron transfer pathway has been evoked rarely in the domain of microbial corrosion. Here was evidenced for the first time that the bacterium Geobacter sulfurreducens is able to increase the free potential of 304 L stainless steel up to 443 mV in only a few hours, which represents a drastic increase in the corrosion risk. In contrast, when the bacterial cells form a locally well-established biofilm, pitting potentials were delayed towards positive values. The microscopy pictures confirmed an intimate correlation between the zones where pitting occurred and the local settlement of cells. Geobacter species must now be considered as key players in the mechanisms of corrosion.     

A Dual-Metal-Catalyzed Sequential Cascade Reaction in an Engineered Protein Cage**

Herein, we describe the creation of an artificial protein cage housing a dual-metal-tagged guest protein that catalyzes a linear, two-step sequential cascade reaction. The guest protein consists of a fusion protein of HaloTag and monomeric rhizavidin. Inside the protein capsid, we established a ruthenium-catalyzed allylcarbamate deprotection reaction followed by a gold-catalyzed ring-closing hydroamination reaction that led to indoles and phenanthridines with an overall yield of up to 66 % in aqueous solutions. Furthermore, we show that the encapsulation stabilizes the metal catalysts against deactivation by air, proteins and cell lysate.