Structural Influences on the Photochemistry and Photophysical Properties of p-Phenylene Ethynylenes: Aggregation Effects and Solvent Interactions

Compounds based on the p-phenylene ethynylene backbone with pendant charged groups, known as conjugated polyelectrolytes, have been of particular interest in recent years due to their solubility in water, sensing properties, and biocidal activity against bacteria, viruses, and fungi. A series of oligomers based on these polymers were synthesized (OPEs), and several interesting questions about their photophysical and biocidal properties were raised by earlier experimental observations, which are addressed by this dissertation. The study initially focuses on the influence of the backbone length and presence of carboxyester substituents on the photophysical properties of the OPEs. Next, the photochemistry of the OPEs is explored as the products and mechanisms are elucidated through isotopic studies with mass spectrometry, revealing that photo-protonation by water and addition of oxygen across the triple bond are the two dominant initial mechanisms of all major pathways in aqueous solution. Finally, the aggregation of OPEs with is studied in two systems: surfactants and model bacterial membranes. The placement of the ionic alkyl substituents played a dominant role in determining the outcome of molecular interactions and type of aggregates which resulted between OPEs and both systems. Biophysical simulations of the interactions between OPEs and these two systems provided mechanistic insight into the mechanism of bacterial membrane disruption and the attenuation of photodegradation observed with OPE-surfactant complexes. In addition to determining the OPEs could be protected from photolysis and the structural basis for aggregate type, surfactant complexation was used to form a biocidal complex from a non-biocidal anionic OPE. The work presented will be of great use for future developments in sensors, biocides, photo-resistant materials, and drug delivery applications

Polarised secretion of leukaemia inhibitory factor

Leukaemia inhibitory factor (LIF) is a cytokine that is active on a wide variety of cells. Multiple LIF transcripts have been described. The transcripts LIF-D and LIF-M encode different signal peptides, which in mouse have been associated with differential localisation of the mature protein. LIF-D is associated with a freely diffusible protein, whereas the LIF-M is associated with the extracellular matrix. The polarity of LIF secretion has yet to be described and could illuminate the mechanisms of LIF localisation. Here the polarised endogenous secretion of human LIF and IL-6 in Caco-2 cells was characterised under normal culture conditions and following induction with IL-1b. Whether the apical or basolateral membrane was stimulated influenced the pattern of secretion (LIF: Unstimulated, 59% basolateral. Dual stimulation, 68% basolateral. Basolateral stimulation, 79% basolateral. Apical stimulation, 53% basolateral). IL-6 displayed a similar dependence on the site of stimulation but was predominantly secreted at the membrane that was stimulated. To determine the effect of the alternate signal peptides on the polarity of LIF secretion, LIF was epitope tagged with FLAG. Epitope-tagging with FLAG was used to separate endogenous from exogenous protein expression. However, despite the normal biological activity of LIF-FLAG and detection of the FLAG in a western blot, detection of the LIF-FLAG under non-reducing conditions was not observed, and therefore it was unsuitable for secretion studies. Untagged LIF was expressed exogenously in Madin-Darby canine kidney (MDCK) cells under the control of a tetracycline response promoter that allowed a variety of LIF expression levels to be tested. Exogenous murine LIF was secreted predominantly from the apical (60%) membrane of MDCK cells irrespective of the signal peptide expressed

Characterization of site-specific GPS errors using a short-baseline network of braced monuments at Yucca Mountain, southern Nevada

We use a short-baseline network of braced monuments to investigate site-specific GPS effects. The network has baseline lengths of ∼10, 100, and 1000 m. Baseline time series have root mean square (RMS) residuals, about a model for the seasonal cycle, of 0.05–0.24 mm for the horizontal components and 0.20–0.72 mm for the radial. Seasonal cycles occur, with amplitudes of 0.04–0.60 mm, even for the horizontal components and even for the shortest baselines. For many time series these lag seasonal cycles in local temperature measurements by 23–43 days. This could suggest that they are related to bedrock thermal expansion. Both shorter-period signals and seasonal cycles for shorter baselines to REP2, the one short-braced monument in our network, are correlated with temperature, with no lag time. Differences between REP2 and the other stations, which are deep-braced, should reflect processes occurring in the upper few meters of the ground. These correlations may be related to thermal expansion of these upper ground layers, and/or thermal expansion of the monuments themselves. Even over these short distances we see a systematic increase in RMS values with increasing baseline length. This, and the low RMS levels, suggests that site-specific effects are unlikely to be the limiting factor in the use of similar GPS sites for geophysical investigations

Isolation of a Novel Phage with Activity against Streptococcus mutans Biofilms

peer-reviewedStreptococcus mutans is one of the principal agents of caries formation mainly, because of its ability to form biofilms at the tooth surface. Bacteriophages (phages) are promising antimicrobial agents that could be used to prevent or treat caries formation by S. mutans. The aim of this study was to isolate new S. mutans phages and to characterize their antimicrobial properties. A new phage, ɸAPCM01, was isolated from a human saliva sample. Its genome was closely related to the only two other available S. mutans phage genomes, M102 and M102AD. ɸAPCM01 inhibited the growth of S. mutans strain DPC6143 within hours in broth and in artificial saliva at multiplicity of infections as low as 2.5x10-5. In the presence of phage ɸAPCM01 the metabolic activity of a S. mutans biofilm was reduced after 24 h of contact and did not increased again after 48 h, and the live cells in the biofilm decreased by at least 5 log cfu/ml. Despite its narrow host range, this newly isolated S. mutans phage exhibits promising antimicrobial properties

Characterization of Longitudinal Splitting and Fiber Breakage in Gr/Ep using Acoustic Emission Data

A composite tensile test specimen was designed such that fiber breakage and longitudinal splitting occurred at a known position in the specimen. By studying the acoustic signature of each failure mechanism distinct characteristics in the data were identified that uniquely related the acoustic emission parameters with either fiber breakage or longitudinal splitting