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Research Topic : CELL MIGRATION
Field of Research : Enzymes
Field of Research : Signal Transduction
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Biochemistry and Cell Biology (8)
Enzymes (8)
Signal Transduction (8)
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  • Researchers (12)
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  • Funded Activity

    Discovery Projects - Grant ID: DP190102285

    Funder
    Australian Research Council
    Funding Amount
    $495,000.00
    Summary
    Molecular determinants of inflammatory caspase activity upon inflammasomes. Most processes fundamental to life rely on the timely, and regulated, execution of cellular functions. The innate immune system, in which both timing and regulation is paramount, rapidly detects invading microbes and induces a measured and timely antimicrobial response to clear infection. This project aims to address a key knowledge gap by characterising a mechanism for timely and controlled immune system activation and .... Molecular determinants of inflammatory caspase activity upon inflammasomes. Most processes fundamental to life rely on the timely, and regulated, execution of cellular functions. The innate immune system, in which both timing and regulation is paramount, rapidly detects invading microbes and induces a measured and timely antimicrobial response to clear infection. This project aims to address a key knowledge gap by characterising a mechanism for timely and controlled immune system activation and immune cell death via the non-canonical inflammasome. We do not currently understand how some immune pathways are turned on or off. This project will yield fundamental insight into mechanisms of mammalian inflammasome, inflammation and anti-microbial responses.
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    Funded Activity

    Discovery Projects - Grant ID: DP160102702

    Funder
    Australian Research Council
    Funding Amount
    $494,400.00
    Summary
    A molecular timer for inflammation and cell death. This project aims to improve our understanding of the timely function of the immune system. Most processes fundamental to life rely on the timely execution of cellular functions. One biological system in which timing is paramount is the immune system. Organismal health relies upon this front-line defence system for rapidly detecting invading microbes and inducing an appropriate, and timely, antimicrobial response to clear infection. We do not cu .... A molecular timer for inflammation and cell death. This project aims to improve our understanding of the timely function of the immune system. Most processes fundamental to life rely on the timely execution of cellular functions. One biological system in which timing is paramount is the immune system. Organismal health relies upon this front-line defence system for rapidly detecting invading microbes and inducing an appropriate, and timely, antimicrobial response to clear infection. We do not currently understand how immune responses are temporally coordinated. This proposal aims to address this key knowledge gap by characterising a novel molecular timer that dictates the co-ordinated timing of immune responses and immune cell death. These studies may yield fundamental insight into mammalian anti-microbial mechanisms.
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    Funded Activity

    Discovery Projects - Grant ID: DP110102641

    Funder
    Australian Research Council
    Funding Amount
    $270,000.00
    Summary
    Structural and functional analysis of the protein kinase R. We have shown that protein kinase R (PKR) plays a key role in regulating the body's response to virus infections, inflammation and cancer. This project will identify mechanisms that regulate the activity of PKR and provide information useful for the development of novel drugs.
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    Active Funded Activity

    Discovery Projects - Grant ID: DP210100665

    Funder
    Australian Research Council
    Funding Amount
    $502,000.00
    Summary
    Regulation of autophagy dependent cell and tissue deletion. This project aims to elucidate novel mechanisms that regulate autophagy-depdendent cell death during animal development. It will combine the power of Drosophila genetics with multidisciplinary approaches, such as proteomics, bioinformatics and cell biology. Given the conserved nature of autophagy the oucomes will provide highly topical and exciting new knowledge of broad biological significance. The project will help establishing inter .... Regulation of autophagy dependent cell and tissue deletion. This project aims to elucidate novel mechanisms that regulate autophagy-depdendent cell death during animal development. It will combine the power of Drosophila genetics with multidisciplinary approaches, such as proteomics, bioinformatics and cell biology. Given the conserved nature of autophagy the oucomes will provide highly topical and exciting new knowledge of broad biological significance. The project will help establishing international collaborations, enhancing Australia’s competitiveness and reputation in an important area of research, and provide training of HDR students in skills across a range of areas. In the long-term the research findings may translate into improved agriculture, food production and human health outcomes.
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    Funded Activity

    Discovery Projects - Grant ID: DP150100936

    Funder
    Australian Research Council
    Funding Amount
    $534,700.00
    Summary
    Developing orthogonal synthetic signaling cascades. This project proposes a generic approach for the construction of molecular switches based on artificially autoinhibited proteases. The bottom-up design of protein-based signaling networks is a key goal of synthetic biology. Yet, this remains elusive due to our inability to tailor-make signal transducers and receptors that can be readily compiled into defined signaling networks. Using structure-guided design and directed protein evolution, a set .... Developing orthogonal synthetic signaling cascades. This project proposes a generic approach for the construction of molecular switches based on artificially autoinhibited proteases. The bottom-up design of protein-based signaling networks is a key goal of synthetic biology. Yet, this remains elusive due to our inability to tailor-make signal transducers and receptors that can be readily compiled into defined signaling networks. Using structure-guided design and directed protein evolution, a set of protease-based signal transducers and ligand activated allosteric receptors will be created. The developed components are intended to be used to construct artificial signaling networks in mammalian cells that are orthogonal to the endogenous signaling cascades.
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    Funded Activity

    ARC Future Fellowships - Grant ID: FT100100100

    Funder
    Australian Research Council
    Funding Amount
    $706,552.00
    Summary
    The discovery and characterisation of novel protein regulators of blood cell formation. All of the mature blood cells in the human body are derived from a common ancestor cell type known as a stem cell. Our proposed studies will enhance our knowledge of how functional, mature blood cells are formed from stem cells and how dysregulation of these normally tightly controlled pathways can give rise to severe blood diseases.
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    Funded Activity

    ARC Future Fellowships - Grant ID: FT110100169

    Funder
    Australian Research Council
    Funding Amount
    $620,628.00
    Summary
    Inhibiting pathological signalling in haematopoietic disease. Certain leukaemias and other blood diseases are caused by the mutation of one particular molecule, called Janus Kinase (JAK), inside our bodies. This project aims to understand the biochemical details of these diseases by studying this mutated molecule in detail. The project will aim to provide the information for developing effective therapeutics against these diseases.
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    Funded Activity

    Discovery Projects - Grant ID: DP110103655

    Funder
    Australian Research Council
    Funding Amount
    $420,000.00
    Summary
    Regulation of neurite outgrowth by an inhibitor of PI3K signalling. PIPP is an enzyme which inhibits important cellular functions such as cell maturation. We have shown the amount of PIPP is increased in Alzheimer's disease brains. This project will characterise the mechanisms by which PIPP regulates brain cell function to identify how PIPP may be acting to exacerbate Alzheimer's disease development/progression.
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    Showing 1-8 of 8 Funded Activites

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