Deeper Insight into Structures of Modified AEROSIL Particles Synthesized via Conventional Heating and Microwave Heating

The contribution deals with the comparison of microwave heating and conventional oil bath heating. Silicon dioxide nanoparticles were grafted with MPTMS under acid conditions. Those particles contain a polysiloxane shell with physically adsorbed and chemically bound fractions which can be separated by Soxhlet extraction. The resulting fractions were analyzed with TGA and MALDI‐TOF MS; one to determine the amount of physically adsorbed and chemically bound fractions and the other to get deeper insight into the polysiloxane structures. Furthermore, it was our aim to clarify which fraction can be visualized using MALDI‐TOF MS. Our results show that the ratio of chemically bound MPTMS is higher when using microwave heating, but the same structures in the physically adsorbed fraction were built in both cases.

     

Polymer/Clay Nanocomposites: Influence of Ionic Strength on the Structure and Adhesion Characteristics in Multilayered Films

The aim of the present contribution is to understand how ionic strength, brought by the addition of salt to laponite/PEO nanocomposite dispersions, influences the texture and adhesion characteristics at nano‐ and microscales in multilayered nanocomposite films prepared from such dispersions. At the nano‐scale, SAXS and XRD measurements indicated that the clay platelets orient parallel to the film plane and that the polymer chains intercalate the clay platelets regardless of salt addition. A gradual transition from an agglomerated structure, containing polymer‐rich and clay‐rich domains, to a fine‐balanced structure with smaller distinct details without excess PEO was observed, via AFM, on the exposed edges of cryo‐microtomed films with increasing ionic strength.

     

Catch strip assay for the relative assessment of two-dimensional protein association kinetics

Accurate interpretation of recruitment rate measurements of microscale particles, such as cells and microbeads, to biofunctional surfaces is difficult because factors such as uneven ligand distributions, particle collisions, variable particle fluxes, and molecular-scale surface separation distances obfuscate the ability to link the observed particle behavior with the governing nanoscale biophysics. We report the development of a hydrodynamically conditioned micropattern catch strip assay to measure microparticle recruitment kinetics. The assay exploited patterning within microfluidic channels and the mechanostability of selectin bonds to create reaction geometries that confined a microbead flux to within 200 nm of the surface under flow conditions. Systematic control of capillary action enabled the creation of homogeneous or gradient ligand distributions. The method enabled the measurement of particle recruitment rates (keff, s-1) that were primarily determined by the interaction of the biomolecular pair being investigated. The method is therefore well suited for relative measurements of delivery vehicle and cellular recruitment potential as governed by surface-bound molecules.     

Two-laser, large-field hyperspectral microarray scanner for the analysis of multicolor microarrays

We describe the development and operation of a two-laser, large-field hyperspectral scanner for analysis of multicolor genotyping microarrays. In contrast to confocal microarray scanners, in which wavelength selectivity is obtained by positioning band-pass filters in front of a photomultiplier detector, hyperspectral microarray scanners collect the complete visible emission spectrum from the labeled microarrays. Hyperspectral scanning permits discrimination of multiple spectrally overlapping fluorescent labels with minimal use of optical filters, thus offering important advantages over standard filter-based multicolor microarray scanners. The scanner uses two-sided oblique line illumination of microarrays. Two lasers are used for the excitation of dyes in the visible and near-infrared spectral regions. The hyperspectral scanner was evaluated with commercially available two-color calibration slides and with in-house-printed four-color microarrays containing dyes with spectral properties similar to their commercial genotyping array counterparts.     

Operation of an X-ray Transition-Edge Sensor Cooled by Tunnel Junction Refrigerators

We demonstrate successful cooling of an X-ray transition-edge sensor (TES) using solid-state refrigerators based on normal-metal/insulator/superconductor (NIS) tunnel junctions. Above the TES transition temperature (T _c ), we use Johnson-noise thermometry to measure the cooling performance. In this regime, the NIS refrigerators cool the TES from 300 mK to 220 mK and from 220 mK to T _c =160 mK. Below T _c , we also observe cooling and demonstrate that the operation of the NIS refrigerators introduces no detectable noise into the TES readout. Contribution of an agency of the U.S. government; not subject to copyright.     

A need for speed: genetic encoding of rapid cycloaddition chemistries for protein labelling in living cells

Rapid reactions: Several reactants for strain-promoted cycloaddition reactions have been genetically encoded as the side chains of noncanonical amino acids. This results in decisive improvements for the fluorescent labelling of intracellular proteins such as quantitative turnover, completion of labelling reactions within minutes, fluorogenic effects and even partial orthogonality for multicolour labelling.     

New and conventional pore size tests in virus-removing membranes

Microorganisms are retained by ultrafiltration (UF) membranes mainly due to size exclusion. The sizes of viruses and membrane pores are close to each other and retention of viruses can be guaranteed only if the precise pore diameter is known. Unfortunately and rather surprisingly, there is no direct method to determine the membrane pore size. As a result, the UF membranes are not trusted to remove the viruses, and the treatment plants are required to enhance viral disinfection.Here we propose a new, simple and effective method for UF pore size determination using aquasols of gold and silver nanoparticles. We synthesized highly monodispersed suspensions ranging in diameter from 3 to 50 nm, which were later transferred through polymer and ceramic UF membranes. The retention percentage was plotted against the particle diameter to determine the pore size for which a membrane has a retention capability of 50, 90 and 100%. The d₅₀, d₉₀ and d₁₀₀ values were compared with data obtained from conventional transmembrane flux, polyethylene glycol, and dextran tests, and with the retention of phi X 174 and MS2 bacteriophages.The absolute pore size, d₁₀₀, for the majority of tested UF membranes is within 40-50 nm, and can only be detected with the new tests. The average 1.2 log retention of hydrophilic phi X 174 was predicted accurately by models based on the virus hydrodynamic radii and d₁₀₀ pore size. The 2.5 log MS2 retention suggests hydrophobic interactions in addition to simple ball-through-cylinder geometry.