Expression of deletion-containing dystrophins in mdx muscle: implications for gene therapy and dystrophin function

The expression of full-length dystrophin and various dystrophin deletion mutants was monitored in mdx mouse muscle after intramuscular injection of dystrophin-encoding plasmid DNAs. Recombinant dystrophin proteins, including those lacking either the amino terminus, carboxyl terminus, or most of the central rod domain, showed localization to the plasma membrane. This suggests that there are multiple attachment sites for dystrophin to the plasma membrane. Only those constructs containing the carboxyl terminus were able to stabilize dystrophin-associated proteins (DAP) at the membrane, consistent with other studies that suggest that this domain is critical to DAP binding. Colocalization with DAP was not necessary for membrane localization of the various dystrophin molecules. However, stabilization and co-localization of the DAP did seem to be a prerequisite for expression and/or stabilization of mutant dystrophins beyond 1 wk and these same criteria seemed important for mitigating the histopathological consequences of dystrophin deficiency.     

Reengineering Through Simulation Modeling

Simulation models are a practical tool for reengineering and redesigning processes and workflows, because they infuse management discussions with the quantitative data needed for sound decision making. The Government Printing Office's use of a discrete-event simulation model helps illustrate the tool's potential to increase revenue, improve customer service, and optimize resource utilization in the area of telephone ordering.     

m-Bromophenolic epoxy resins for electronic packaging

Meta-halogenated phenols are generally known to be more chemically and thermally stable than their ortho- or para-halogenated counterparts. A reactive intermediate, produced by the bromination of 2,4,6-trimethylphenol is being used as an alkylating agent to incorporate this stable m-bromophenol moiety into varieties of organic compounds and polymers. In electronic encapsulation applications, epoxy derivatives of novolacs containing m-bromophenol have exhibited superior hydrolytic and thermal stability as compared with the conventional tetrabromo bisphenol-A epoxies which are ortho-brominated phenolics. The m-bromophenol moiety contributes to the extended device reliability while meeting flame retardency requirements as well.     

Development of an incremental rolling process for the production of defined riblet surface structures

Viscous drag reduction on fan, compressor and turbine blades may be achieved by employing a riblet surface structure. Such a structure assists in increasing efficiency and in reducing energy consumption in flow applications. In order to produce riblet surface structures industrially, a new and incremental rolling process is being developed and investigated. The process design is being determined by common airstream requirements as well as the forming mechanisms that are predominant during the rolling process. Based on this principle, the required shape of the structured rollers is being developed. Research is focused on the feasibility of manufacturing small riblet structures at a size of a few hundred microns. Experimental production of different riblet geometries made from Ti-6Al-4V (WL 3.7164) provides some initial insights with respect to feasibility, shape accuracy, surface quality, and micro structure.     

Comparison of T1-weighted 2D TSE, 3D SPGR,and two-point 3D Dixon MRI for automated segmentation of visceral adipose tissue at 3 Tesla

Objectives

To evaluate and compare conventional T1-weighted 2D turbo spin echo (TSE), T1-weighted 3D volumetric interpolated breath-hold examination (VIBE), and two-point 3D Dixon-VIBE sequences for automatic segmentation of visceral adipose tissue (VAT) volume at 3 Tesla by measuring and compensating for errors arising from intensity nonuniformity (INU) and partial volume effects (PVE).

Materials and methods

The body trunks of 28 volunteers with body mass index values ranging from 18 to 41.2 kg/m² (30.02 ± 6.63 kg/m²) were scanned at 3 Tesla using three imaging techniques. Automatic methods were applied to reduce INU and PVE and to segment VAT. The automatically segmented VAT volumes obtained from all acquisitions were then statistically and objectively evaluated against the manually segmented (reference) VAT volumes.

Results

Comparing the reference volumes with the VAT volumes automatically segmented over the uncorrected images showed that INU led to an average relative volume difference of ?59.22 ± 11.59, 2.21 ± 47.04, and ?43.05 ± 5.01 % for the TSE, VIBE, and Dixon images, respectively, while PVE led to average differences of ?34.85 ± 19.85, ?15.13 ± 11.04, and ?33.79 ± 20.38 %. After signal correction, differences of ?2.72 ± 6.60, 34.02 ± 36.99, and ?2.23 ± 7.58 % were obtained between the reference and the automatically segmented volumes. A paired-sample two-tailed t test revealed no significant difference between the reference and automatically segmented VAT volumes of the corrected TSE (p = 0.614) and Dixon (p = 0.969) images, but showed a significant VAT overestimation using the corrected VIBE images.

Conclusion

Under similar imaging conditions and spatial resolution, automatically segmented VAT volumes obtained from the corrected TSE and Dixon images agreed with each other and with the reference volumes. These results demonstrate the efficacy of the signal correction methods and the similar accuracy of TSE and Dixon imaging for automatic volumetry of VAT at 3 Tesla.

     

Platinum-plated nanoporous gold: An efficient,low Pt loading electrocatalyst for PEM fuel cells

Platinum-plated nanoporous gold leaf (Pt-NPGL) is made by coating a conformal, atomically thin skin of platinum over the high surface area pores of a thin membrane of nanoporous gold. Because Pt loading in Pt-NPGL can be controlled down to 0.01 mg cm⁻² using only simple benchtop chemistry, the material holds promise as a low Pt loading, carbon-free electrocatalyst. Here, we report successful use of Pt-NPGL as a catalyst in proton exchange membrane (PEM) fuel cells. Stable and high performance Pt-NPGL/Nafion membrane electrode assemblies (MEAs) were made using a stamping technique. The performance of Pt-NPGL MEAs is comparable to conventional carbon-supported nanoparticles-based MEAs with much higher loading, generating an output power density of up to 4.5 kW g⁻¹ Pt in our non-optimized test configuration. Correlations between the performance of Pt-NPGL MEAs, the electrochemically accessible surface area, and material microstructure are discussed. Our success in using Pt-NPGL as a fuel cell catalyst suggests that creating precious metals skins over nanoporous metal supports is a viable strategy for designing new catalysts for PEM fuel cells. This promising approach allows tailoring catalytic activity by engineering precious metal/substrate interactions, employs materials with dual functionality acting both as current collector and catalyst, and may avoid the sintering problems plaguing conventional nanoparticle-based catalysts.