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Status : Active
Field of Research : Biological Physics
Australian State/Territory : ACT
Research Topic : Solar physics
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  • Active Funded Activity

    ARC Future Fellowships - Grant ID: FT180100100

    Funder
    Australian Research Council
    Funding Amount
    $728,125.00
    Summary
    Single spin molecular microscope. This project aims to create a new tool for imaging and analysing material at the atomic level. The tool is based on individual quantum coherent spins in diamond which can be manipulated and optically read. The project expects to generate knowledge in quantum metrology and an understanding of molecular dynamics at the nanoscale. The expected outcome is a new type of device capable of imaging complex physical systems at the level of their individual constituent co .... Single spin molecular microscope. This project aims to create a new tool for imaging and analysing material at the atomic level. The tool is based on individual quantum coherent spins in diamond which can be manipulated and optically read. The project expects to generate knowledge in quantum metrology and an understanding of molecular dynamics at the nanoscale. The expected outcome is a new type of device capable of imaging complex physical systems at the level of their individual constituent components. This has significant benefits in improving designer materials, energy production, information storage, and drug design.
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    Active Funded Activity

    Linkage Infrastructure, Equipment And Facilities - Grant ID: LE210100046

    Funder
    Australian Research Council
    Funding Amount
    $289,381.00
    Summary
    A fast fluorescence lifetime imaging microscope to track protein dynamics. This project aims to establish a fast fluorescence lifetime imaging microscope that can track the intracellular journey of a protein throughout the entire structural framework of a living cell. By coupling single particle tracking technology with a cutting-edge fluorescence lifetime camera, this one-of-a-kind microscope will enable protein mobility and interaction to be spatially mapped with unprecedented temporal resolut .... A fast fluorescence lifetime imaging microscope to track protein dynamics. This project aims to establish a fast fluorescence lifetime imaging microscope that can track the intracellular journey of a protein throughout the entire structural framework of a living cell. By coupling single particle tracking technology with a cutting-edge fluorescence lifetime camera, this one-of-a-kind microscope will enable protein mobility and interaction to be spatially mapped with unprecedented temporal resolution. The benefit of this technology is that it will enable scientists in Australia to image, for the first time, the biophysical mechanism by which a protein navigates intracellular architecture to regulate a complex biological function at the single molecule level.
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    Active Funded Activity

    Discovery Projects - Grant ID: DP200100364

    Funder
    Australian Research Council
    Funding Amount
    $470,000.00
    Summary
    5D Imaging Flow Cytometry for in vivo Quantification of Biological Fluids. Rapid and accurate quantification of live biological fluid properties at sub-cellular and molecular levels forms the bedrock of biofluidic sciences. Majority of the biofluidic devices rely on quantifying biological fluids after its removal from the body in an in vitro Flow Cytometer (FC). FC faces many caveats i.e. biological degradation and small volume etc. In this project, we shall engineer the first in vivo 5D imaging .... 5D Imaging Flow Cytometry for in vivo Quantification of Biological Fluids. Rapid and accurate quantification of live biological fluid properties at sub-cellular and molecular levels forms the bedrock of biofluidic sciences. Majority of the biofluidic devices rely on quantifying biological fluids after its removal from the body in an in vitro Flow Cytometer (FC). FC faces many caveats i.e. biological degradation and small volume etc. In this project, we shall engineer the first in vivo 5D imaging flow cytometer (5D IFC) capable of continuous assessment of potentially entire blood volume in a living mice without removing fluid out of the body. The project represents a major advancement beyond any existing flow cytometer and overcome the engineering limits of state-of-art laser scanning imaging devices.
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    Active Funded Activity

    Discovery Projects - Grant ID: DP200100338

    Funder
    Australian Research Council
    Funding Amount
    $390,000.00
    Summary
    Photosynthesis under extreme conditions. The aim of this project is to characterise modifications to the light dependent reactions of photosynthesis of simple, single cell organisms that live under harsh environmental conditions including: i) elevated temperature; ii) low, variable and low energy (red) light; iii) arid and variable hydration; and iv) chemical stress e.g. low pH. In a changing biosphere brought about by anthropological climate change, a better understanding of existing adaptions .... Photosynthesis under extreme conditions. The aim of this project is to characterise modifications to the light dependent reactions of photosynthesis of simple, single cell organisms that live under harsh environmental conditions including: i) elevated temperature; ii) low, variable and low energy (red) light; iii) arid and variable hydration; and iv) chemical stress e.g. low pH. In a changing biosphere brought about by anthropological climate change, a better understanding of existing adaptions of bacterial photosynthetic organisms may allow more resilient crops and other essential plants to be developed in the future. The project brings together an international consortium of world renowned experts across key aspects of photosynthesis.
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    Active Funded Activity

    Discovery Projects - Grant ID: DP190100510

    Funder
    Australian Research Council
    Funding Amount
    $470,000.00
    Summary
    Molecular mechanisms of mechanosensation and shape regulation in cells. This project aims to explore how cells physically sense and respond to the surrounding environment on a molecular level. Physical distortion of erythrocytes doubles their glucose consumption and increases cation membrane flux five-fold. This mechanism involves opening of the mechanosenstive ion channel Piezo1. This project will include a kinetic description of these phenomena, with a goal to establish a predictive mathematic .... Molecular mechanisms of mechanosensation and shape regulation in cells. This project aims to explore how cells physically sense and respond to the surrounding environment on a molecular level. Physical distortion of erythrocytes doubles their glucose consumption and increases cation membrane flux five-fold. This mechanism involves opening of the mechanosenstive ion channel Piezo1. This project will include a kinetic description of these phenomena, with a goal to establish a predictive mathematical model of the regulation of cell-shape and volume. The project will provide an understanding of mechanisms operating when cells and tissues are succumbing to trauma and invasion, and how to control these processes on a molecular level.
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