Discovery Early Career Researcher Award - Grant ID: DE120100467
Funder
Australian Research Council
Funding Amount
$375,000.00
Summary
Unravelling the intrinsic structure and stability of multiply charged anions in the gas-phase using photoelectron spectroscopy and mass spectrometry. Molecules possessing multiple negative charges are common constituents in chemistry, influencing a range of processes ranging from photochemical smog formation to protein structure in vivo. This project will develop new technologies to probe their molecular structure in the gas-phase, leading to a more rigorous understanding of these species.
New laser and mass spectrometry-based tools for comprehensive structural elucidation of lipids and their biomolecular interactions. Lipid-related disorders such as obesity, diabetes and heart disease are reaching epidemic proportions. We propose the development of specialised instrumentation to identify and quantify lipids (fats) in tissue and culture samples thus providing Australian scientists with unique capabilities to investigate the mechanisms of disease.
Linkage Infrastructure, Equipment And Facilities - Grant ID: LE120100059
Funder
Australian Research Council
Funding Amount
$220,000.00
Summary
Multiplexed capabilities for surface analysis and imaging by mass spectrometry. This facility will support research aimed at developing rapid and reliable analytical methods for the detection of chemicals directly from biological and man-made materials. The mass spectroscopy methods used at the facility will reveal molecular-level changes in systems ranging from the lens of the human eye to Colorbond steel® and have applications in the detection of chemical and biological hazards.
Spectroscopic investigations into nano-scale drug interactions and molecular processes in single living cells and isolated molecules. This project will develop micro-spectroscopy and nano-spectroscopy molecular imaging based techniques to spatially locate and determine the bonding sites of a new range of chemotherapeutic drugs designed to treat cancer and malaria. This project will adopt a translational approach looking first at drug interactions directly with molecules such as DNA. Secondly, in ....Spectroscopic investigations into nano-scale drug interactions and molecular processes in single living cells and isolated molecules. This project will develop micro-spectroscopy and nano-spectroscopy molecular imaging based techniques to spatially locate and determine the bonding sites of a new range of chemotherapeutic drugs designed to treat cancer and malaria. This project will adopt a translational approach looking first at drug interactions directly with molecules such as DNA. Secondly, investigating these interactions in living cells and finally applying the technology to tissue samples. The outcome of this research will be new drug screening technologies and methodologies to address two of the most devastating diseases to afflict human kind, offering hope to the countless millions suffering from these diseases.Read moreRead less
Rapid, ultra-sensitive protein structure elucidation by mass spectrometry. This project seeks to develop a method for rapidly discovering classes of molecules that bind to unique sites on proteins. The development of new pharmaceuticals is frequently delayed by the time and resources required to identify the sites that new chemical entities bind to protein targets. A recent discovery has resulted in the ability to completely characterise large protein sequences directly from single mass spectra. ....Rapid, ultra-sensitive protein structure elucidation by mass spectrometry. This project seeks to develop a method for rapidly discovering classes of molecules that bind to unique sites on proteins. The development of new pharmaceuticals is frequently delayed by the time and resources required to identify the sites that new chemical entities bind to protein targets. A recent discovery has resulted in the ability to completely characterise large protein sequences directly from single mass spectra. This project aims to leverage this breakthrough by developing a rapid new approach for revealing ligand-protein binding sites using whole-protein mass spectrometry. This would enable novel sites of interactions between molecules and protein targets to be discovered rapidly with high sensitivity. In turn, this would allow the efficient design of next-generation classes of bioactive molecules.Read moreRead less