183 research outputs found
Development of Transparent LSCO and LSCNO Conductors for Optical Shutter Systems
We have prepared lanthanum strontium cobalt oxide (La0.50Sr0.50CoO3; LSCO 50/50) and lanthanum strontium cobalt nickel oxide (La0.50Sr0.50Co0.50Ni0.50O3; LSCNO) as candidate transparent electrodes for use in a shutter-based infrared sensor protection device. The shutter device requires that the electrode be transparent (80% transmission) and have moderate sheet resistance (300 Ω/sq.). Because of the effects of film thickness on intrinsic material properties, such as resistivity and extinction coefficient, and simple engineering issues (i.e., the relationship between film thickness, resistance and transmission), films of various thicknesses were prepared to achieve an optimal balance of electrical and optical performance. van der Pauw measurements and FTIR spectroscopy were used to study thin film properties. The best LSCO films prepared demonstrated electrical (438 Ω/sq.) and optical (68% transmission at 8 μm) properties that did not meet the target property goals for this application. However, the LSCNO films (of optimal thickness) offered performance (323 Ω/sq. and 73% transmission) close to the device requirements
A membrane component essential for vectorial translocation of nascent proteins across the endoplasmic reticulum: requirements for its extraction and reassociation with the membrane.
Characterization of molecules involved in protein translocation using a specific antibody.
The identification of proteins in the proximity of signal-anchor sequences during their targeting to and insertion into the membrane of the ER.
Transport of Proteins into Mitochondria
The mitochondrial ADP/ATP carrier is an integral transmembrane protein of the inner membrane. It is synthesized on cytoplasmic ribosomes. Kinetic data suggested that this protein is transferred into mitochondria in a posttranslational manner. The following results provide further evidence for such a mechanism and provide information on its details.
1. In homologous and heterologous translation systems the newly synthesized ADP/ATP carrier protein is present in the postribosomal supernatant.
2. Analysis by density gradient centrifugation and gel filtration shows, that the ADP/ATP carrier molecules in the postribosomal fraction are present as soluble complexes with apparent molecular weights of about 120000 and 500000 or larger. The carrier binds detergents such as Triton X-100 and deoxycholate forming mixed micelles with molecular weights of about 200000–400000.
3. Incubation of a postribosomal supernatant of a reticulocyte lysate containing newly synthesized ADP/ATP carrier with mitochondria isolated from Neurospora spheroplasts results in efficient transfer of the carrier into mitochondria. About 20–30% of the transferred carrier are resistant to proteinase in whole mitochondria. The authentic mature protein is also largely resistant to proteinase in whole mitochondria and sensitive after lysis of mitochondria with detergent. Integrity of mitochondria is a prerequisite for translocation into proteinase resistant position.
4. The transfer in vitro into a proteinase-resistant form is inhibited by the uncoupler carbonyl-cyanide m-chlorophenylhydrazone but not the proteinase-sensitive binding.
These observations suggest that the posttranslational transfer of ADP/ATP carrier occurs via the cytosolic space through a soluble oligomeric precursor form. This precursor is taken up by intact mitochondria into an integral position in the membrane. These findings are considered to be of general importance for the intracellular transfer of insoluble membrane proteins. They support the view that such proteins can exist in a water-soluble form its precursors and upon integration into the membrane undergo a conformational change. Uptake into the membrane may involve the cleavage of an additional sequence in some proteins, but this appears not to be a prerequisite as demonstrated by the ADP/ATP carrier protein
Sec61p is adjacent to nascent type I and type II signal-anchor proteins during their membrane insertion.
The signal sequence receptor has a second subunit and is part of a translocation complex in the endoplasmic reticulum as probed by bifunctional reagents.
Beyond the ‘Tomlinson Trap’: analysing the effectiveness of section 1 of the Compensation Act 2006
One of the intentions underpinning section 1 of the Compensation Act 2006 was to provide reassurance to individual volunteers, and voluntary organisations, involved in what the provision called ‘desirable activities’ and including sport. The perception was that such volunteers, motivated by an apprehension about their increased vulnerability to negligence liability, and as driven by a fear of a wider societal compensation culture, were engaging excessively in risk-averse behaviour to the detriment of such socially desirable activities. Academic commentary on section 1 of the Compensation Act 2006 has largely regarded the provision as unnecessary and doing little more than restating existing common law practice. This article argues otherwise and, on critically reviewing the emerging jurisprudence, posits the alternative view that section 1, in practice, affords an enhanced level of protection and safeguarding for individuals undertaking functions in connection with a desirable activity. Nonetheless, the occasionally idiosyncratic judicial interpretation given to term ‘desirable activity’, potentially compounded by recent enactment of the Social Action, Responsibility and Heroism Act 2015, remains problematic. Two points of interest will be used to inform this debate. First, an analysis of the then House of Lords’ decision in Tomlinson and its celebrated ‘balancing exercise’ when assessing reasonableness in the context of negligence liability. Second, a fuller analysis of the application of section 1 in the specific context of negligence actions relating to the coaching of sport where it is argued that the, albeit limited, jurisprudence might support the practical utility of a heightened evidential threshold of gross negligence
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