School of Chemistry - Theses

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    Exploring novel blue turn-on fluorescent probes for the direct detection of nitric oxide and free radicals in living cells
    Barzegaramiriolya, Mina ( 2017)
    Bacterial biofilms are causing considerable damage to different areas in industry such as food industry, oil industry and dentistry. Traditional methods to control biofilm formation and to treat the surfaces affected by these microorganisms has mostly focused on biocidal and antibacterial strategies. The drawbacks of these approaches is related to the development of tolerances that decrease effectiveness of chemicals apply to eradicate these microorganisms. The growth of biofilms therefore is linked to a significant adaptation by bacteria cells to control changes in their environment. In this regard, the development of efficient methods to control biofilms formation as well as their irreversible eradication from affected surfaces is an important area of scientific research. Bacterial biofilms at times undergo regulated and coordinated dispersal events, where sessile biofilm cells convert to free-swimming, planktonic bacteria. Nitric oxide (NO) is an important biochemical signalling molecule that has been linked to the inhibition of biofilm formation and activation of dispersal through the generation of nitrosative and oxidative stress. Therefore, the availability of methods that enable sensing and visualizing NO is critical to reveal details of the biological functioning of this molecule. Knowledge of these will provide important guidelines for the development of strategies to combat biofilm formation. In this thesis two different approaches for detecting NO and oxidative stress were explored, that are based on fluorescence measurements using coumarin as fluorophore. The first strategy explores “turn-on” fluorescence for direct detection of endogenously produced NO. A family of five blue fluorescent probes CB1-5 were designed and synthesized and the photophysical properties studied in detail. These probes feature a substituted 7-hydroxy coumarin chromophore coupled to 2-methyl-8-aminoquinoline, which act as tridentate ligand for Cu(II) and active site for monitoring NO using the replacement strategy. The UV-vis absorption and fluorescence emission characteristics of the probes are significantly influenced by the substitution pattern on the coumarin ring, as well as by solvent polarity and pH. Time-dependent Density Functional Theory (TD-DFT) calculations for CB4 and CB5 showed that the absorptions are due to π ® π* transitions localised on the coumarin system, with a small charge transfer contribution from the quinoline system at higher pH where the 7-hydroxycoumarin moiety is deprotonated. Complexation of the probes with Cu(II) leads to fluorescence quenching, which switches back on upon reaction with NO. In vitro studies revealed that the probes detect NO with high selectivity in nM concentrations and do not respond to other oxidizing species. In vivo studies for CB4 and CB5 showed that these probes enable detection of NO in living bacterial cells in multi-dye imaging experiments. Furthermore, CB5 also enables to detect NO in macrophages, where it is an important effector molecule in host defence against bacterial pathogens. Using confocal microscopy, it was shown that the probe can be trapped by the cells and reacts directly and specifically with NO, rendering it a promising tool for imaging NO in response to pharmacological agents that modulate its level, for example during bacterial infections. The second strategy explored in this work was the development of a profluorescent nitroxide probe, which can be utilized for detecting the formation of reactive nitrogen and oxygen intermediates and associated changes in redox states within microcolonies. Attachment of a nitroxide to a fluorophore leads to fluorescence quenching, which upon free radical scavenging, metabolism or redox processes, returns the molecule to its native fluorescent state. A large variety of synthetic approaches and procedures were explored to construct such structure, but unfortunately none of them were successful.
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    Photophysical studies of 2-aminopurine in DNA
    McKenzie, Grant ( 2017)
    Deoxyribonucleic acid (DNA) forms the basis of all known living organisms. Despite the essential role played by DNA, its dynamic system and functional behaviour are still not completely understood. The work presented in this thesis aims to explore the structural dynamics of DNA systems, using fluorescence-based approaches, and to attempt to develop a technique for the measurement of fluorescence decays of biological molecules on the ultrafast (femtosecond) timescale. Absorption of UV radiation by DNA is known to lead to mutations and damage to DNA structure and functionality. For the majority of absorbed photons, the excitation energy dissipates harmlessly as heat, but in some instances this energy transfers to regions of DNA that are more susceptible to damage. 2-Aminopurine (2AP), a fluorescent analogue of the native DNA base adenine, can be incorporated into DNA with minimal perturbation to the DNA structure, and can be used to investigate inter-base electronic energy transfer. By selectively exciting the native DNA base in 2AP-containing dinucleotides and utilising 2AP fluorescence as an energy acceptor, the mechanism of electronic energy transfer has been investigated. Analysis of the resulting fluorescence lifetimes of 2AP has revealed that energy transfer preferentially excites conformations in which the bases are highly stacked, and the fluorescence of 2AP is highly quenched. This has led to a re-evaluation of energy transfer efficiencies between the natural bases and 2AP, and has shown that transfer efficiencies cannot be determined correctly from steady-state fluorescence measurements. To investigate the influence of base dynamics on the quenching of 2AP fluorescence in DNA, time-resolved fluorescence measurements were carried out on 2AP-containing systems in frozen solution at 77 K. These studies included dinucleotides, single–strand oligonucleotides and their corresponding duplexes. In all cases, comparison of the fluorescence decay parameters measured at room temperature with those measured at 77 K showed that elimination of base dynamics prevented rapid quenching, on the 10s of ps timescale or faster, although quenching on the 100s of ps timescale persisted for 2AP in single strands and duplexes. The multi-exponential fluorescence decay of 2AP in DNA and its high sensitivity to local environment is commonly exploited to investigate DNA-enzyme interactions. Transposases are enzymes involved in the movement of sections of DNA (transposons) within the genome. The Mos1 transposase catalyses the movement of a transposon via a cut-and-paste mechanism involving several intermediate complexes. Understanding the complex mechanism by which the transposase can remove and insert a section of DNA would allow these enzymes to be used as biomolecular tools. The structure of the intermediate Mos1 strand-transfer complex (STC) has been investigated by incorporating 2AP into several regions of the transposon and analysing the fluorescence decay. The involvement of a base-flipping-like mechanism has been identified in the mechanism of strand transfer for the Mos1 transposon. The time-resolved fluorescence measurements performed in this thesis are limited to time resolution of ~20 ps and longer using TSCPC. However, an abundance of photophysical events in DNA occur on the femtosecond timescale. Development of a methodology utilising fluorescence gating techniques (such as sum-frequency generation or diffraction from a transient grating) have been attempted, in order to construct an experimental system that enables the broadband detection of ultrafast fluorescence decays. Despite the lack of immediate success in recording the fluorescence decay from a sample, due to technical issues and time-constraints, initial characterisation of the set-up was performed and the prospect of broadband detection was demonstrated. Overall, this thesis gives insight into some of the dynamic processes taking place in DNA and presents work performed to develop a system that would allow the extension of these studies to processes occurring on the fs timescale.
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    Imaging the interactions of antimicrobial peptides with model and living cellular membrane systems
    Burton, Matthew Grant ( 2016)
    Since the discovery of penicillin over 80 years, the use of antimicrobial compounds has undoubtedly been one of the greatest contributions to modern science and medicine. Due to their use, misuse, and abuse over this time, numerous bacterial species have developed countermeasures to resist the effects of these antimicrobials. This rise in antimicrobial resistance has continued unabated since their first use, and now has the potential for devastating costs to humanity on a global scale; notably, mortality rates well into the millions over the coming decades. In turn, this has sparked interest in new therapeutic options not based on currently existing compounds. Antimicrobial Peptides (AMPs) are one such class of compounds. They can be found in virtually all forms of life, and act as the first-line- of-defence against a broad spectrum of pathogens at very low concentrations with limited resistance capacity. This makes AMPs extremely lucrative for future therapeutic design. Despite extensive investigations into their interactions, detailed mechanistic information about their behaviour with membranes remains elusive. Numerous models have been proposed to account for the observed behaviour of cell death, including pore-formation, detergent action, or some combination of the two. Mechanistic information regarding the progression of these models remains limited, however. In this work, we investigate the mechanistic behaviour of a model AMP with artificial and living bacterial membranes, primarily through the means of time- resolved fluorescence microscopy techniques. The antimicrobial peptide under study is an analogue of melittin; a well-characterised lytic peptide that displays significant activity to both eukaryotic and prokaryotic membranes. The analogue also bears a proline-to-lysine substitute around the centre of the peptide sequence, to which the fluorescent probe Alexa Fluor 430 is grafted. Using known photophysical information of the fluorescent peptide, information regarding the mechanistic progression of its interaction with membranes can be observed and deconvolved. This research progresses from developing a simple mechanistic understanding using model membrane systems, to increasingly complex living systems. In the liposome giant vesicle model, a slow two-step pore-formation mechanism was found to fit to the observed data, with major significance on the roles of aggregates. Leakage studies using the same liposome system found that the same pore-forming mechanism occurred in both unilamellar and multilamellar membranes, but with dramatically reduced pore stability in the latter. Similar experiments on E. coli bacteria revealed a more complex interaction that could not be adequately explained using either model systems. This finding has important ramifications for correlating information gained from model studies to living membranes. Finally, peptide interactions with Pseudomonas aeruginosa L-Forms were investigated in detail for the first time using super-resolution and fluorescence lifetime microscopies. The use of a biologically relevant environment was found to drastically alter the observed outcome of the peptide-membrane interaction, although the importance of peptide aggregates remains. Furthermore, little change in the fluorescence lifetime is observed over time, despite a clear time-resolved killing mechanism. The reasons for this, and the potential importance of the L-Form state, are explored in detail.
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    Investigating the structure and dynamics of DNA with fluorescence and computational techniques
    Smith, Darren Andrew ( 2014)
    Nucleic acids, such as DNA, play an essential role in all known forms of life; however, despite their fundamental importance, there is still a significant lack of understanding surrounding their functional behaviour. This thesis explores the structure and dynamics of DNA by employing methods based on fluorescence and through the use of computational calculations. Time-resolved fluorescence experiments have been performed on dinucleotides containing 2-aminopurine (2AP) in various alcohol-water mixtures. 2AP, a fluorescent analogue of the nucleobase adenine, has been used extensively to investigate nucleic acids because of its ability to be incorporated into their structures with minimal perturbation and its high sensitivity to its local environment. Direct solvent effects on 2AP were established through measurements on the free fluorophore. Analysis of the complex fluorescence decays associated with the dinucleotides was challenging but has provided insight into their conformational dynamics. Solvent polarity was found to play a significant role in determining both photophysical and conformational properties in these systems. The complicated fluorescence decay of 2AP in nucleic acids highlights the need for accurate and unbiased analysis methods. Various time-resolved fluorescence analysis methods, including iterative reconvolution and the exponential series method, have been investigated with real and simulated data to obtain an overview of their benefits and limitations. The main outcome of the evaluation is that no single method is preferred in all situations and there is likely to be value in using a combination when there is ambiguity in the interpretation of the results. Regardless of the analysis technique used, the parameterised description of the observed fluorescence decay is meaningless if the underlying physical model is unrealistic. The advance of computational methods has provided a new means to rigorously test the viability of proposed models. Calculations have been performed at the M06-2X/6-31+G(d) level of theory to investigate the stability of 2AP-containing dinucleotides in conformations similar to those observed in the double-helical structure of DNA. The results help to explain the similarity of the time-resolved fluorescence behaviour of 2AP in dinucleotide and DNA systems but also bring to light subtle differences that could perhaps account for experimental discrepancies. The recent emergence of advanced optical microscopy techniques has offered the prospect of being able to directly visualise nucleic acid structure at the nanoscale but, unfortunately, limitations of existing labelling methods have hindered delivery of this potential. To address this issue, a novel strategy has been used to introduce reversible fluorescence photoswitching into DNA at high label density. Photophysical studies have implicated aggregation and energy-transfer as possible quenching mechanisms in this system, which could be detrimental to its future application. The reliability of fluorescence photoswitching was investigated at ensemble and single-molecule level and by performing optical lock-in detection imaging. These developments lay the foundations for improved and sequence-specific super-resolution microscopy of DNA, which could offer new insights into the 3D nanoscale structure of this remarkable biopolymer. In summary, the work presented in this thesis outlines important observations and developments that have been made in the study of the structure and dynamics of nucleic acids.
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    Assessment of perylene-based profluorescent nitroxides for monitoring polyester degradation upon weathering
    SYLVESTER, PAUL ( 2013)
    A profluorescent nitroxide possessing an isoindoline nitroxide moiety linked to a perylene fluorophore was developed to monitor radical mediated degradation of melamine-formaldehyde crosslinked polyester coil coatings in an industry standard accelerated weathering tester. Trapping of polyester derived radicals (most likely C-radicals) that are generated during polymer degradation leads to fluorescent closed-shell alkoxy amines. Time-dependent degradation profiles were generated to assess the relative stability of different polyesters towards weathering. The nitroxide probe couples excellent thermal stability and satisfactory photostability with high sensitivity and enables detection of free radical damage in polyesters under conditions that mimic exposure to the environment on a time scale of hours rather than months or years required by other testing methods. There are indications that the profluorescent nitroxide undergoes partial photodegradation in the absence of polymer derived radicals. It was also found that UV-induced fragmentation of the NO-C bond in closed-shell alkoxy amines leads to regeneration of the profluorescent nitroxide and the respective C-radical. The maximum fluorescence intensity that could be achieved with a given probe concentration is therefore not only determined by the amount of polyester radicals formed during accelerated weathering, but also by the light-driven side reactions of the profluorescent nitroxide and the corresponding alkoxy amine radical trapping products. Studies to determine the optimum probe concentration in the polymer matrix revealed that aggregation and reabsorption effects lowered the fluorescence intensity at higher concentrations of the profluorescent nitroxide, but lower probe concentrations, where these effects would be avoided, were not sufficient to trap the amount of polyester radicals formed upon weathering. The optimized experimental conditions were used to assess the impact of temperature and UV irradiance on polymer degradation during accelerated weathering.
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    Synthesis and application of molecular probes for biologically important metal ions
    BUNCIC, GOJKO ( 2012)
    The synthesis and characterization of new molecular probes aimed towards studies with metal ions in biology is described. One synthetic platform involves 1,2-phenylenediamine-based ligands which are divided into two classes. The first consists of ligands with carboxylic acid functional groups. These resemble the classic hexadentate ligand H4Edta. Previous studies demonstrated that functional groups substituted at the aromatic backbone affect the binding affinities for metal ions. This proves a way of preparing a family of ligands with similar coordination properties but different binding affinities. Interesting cobalt complexes were characterised by single crystal X-ray diffraction studies. Two cobalt atoms, each complexed to one ligand in a single crystal of one of the complexes, had different coordination geometries. A fluorescent group Bodipy was successfully attached to the aromatic backbone to make a new water soluble probe which exhibited a 2-fold fluorescence enhancement in presence of Zn(II). A second class of 1,2-phenylenediamine-based ligands was established by preparation of aminopyridine ligands, which were designed to optimize selectivity for Cu(II) and Cu(I) ions. A particular focus was the length of the linker to the pyridine arms for flexible coordination around the metal centre, with a particular Cu(II) complex demonstrating the point. Interesting redox behaviours were observed in the preparation of copper complexes. One ligand H2L binds Cu(I) to form salt [CuI(H2L)]BF4 which undergoes aerial oxidation in solution. A diamagnetic salt [CuIIL•-]BF4 was isolated where π-radical anion L•- is the (1e-, 2H+) oxidation product of H2L. This analysis was confirmed by a number of techniques including monitoring of the oxidation process by electrochemistry and electronic and NMR spectroscopies. The second synthetic platform focused on bis(thiosemicarbazone) compounds. New water soluble ligands were prepared by selective transamination reactions using sulfanilic acid as the transaminating group. Studies with the new ligands revealed that good water solubility, 1:1 binding stoichiometry and the ability of ligands to form chromophoric species with Zn(II) with buffered solutions make them potential molecular probes for studies with this ion. An affinity of KD = 6.0 x 10-9 M-1 for Zn(II) was determined for one ligand Na[H2L7] via competition assays with H2Egta2-. The new ligand was applied in estimating the binding affinities of two plant proteins.
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    Synthesis and study of organic light emitting materials
    Raja, Inam ul Haq ( 2011)
    Since the discovery of electroluminesence from organic materials, there has been a considerable amount of research, time and efforts devoted to developing conjugated materials as the active units in light emitting devices for use in display applications. This thesis describes the synthesis and study of organic materials to achieve high efficiency in organic light emitting devices (OLEDs). A number of blue fluorescent and green to blue phosphorescent host polymers based on dibenzophosphole oxides have been synthesized and studied. Effect of the structure of polymer backbone and different substituents on optical properties has been studied and described. In addition, the synthesis and the study of polymers based on phosphine oxides have been described which are potential charge-transporting high triplet energy materials. All these polymers are thermally stable, blue fluorescent, potential hosts for green and blue phosphorescent guests and expected to facilitate charge transport in OLEDs.