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Funding Provider : Australian Research Council
Research Topic : AMINO ACID
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Medical Biochemistry: Amino Acids and Metabolites (6)
Animal Physiology - Cell (2)
Biochemistry and Cell Biology (2)
Medical Biochemistry and Metabolomics (2)
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  • Active Funded Activity

    Discovery Projects - Grant ID: DP190101937

    Funder
    Australian Research Council
    Funding Amount
    $499,000.00
    Summary
    Age-related mechanisms of amino acid signalling in skeletal muscle. This project aims to increase our understanding of the role of glycine receptor-mediated signalling and its metabolism in the amino acid sensing capacity of mTORC1, a key enzyme regulating muscle protein synthesis. Ageing is associated with a progressive decline in skeletal muscle mass, weakness, and impaired regeneration after injury. Impaired anabolic signalling after food intake has been proposed as a key contributor, yet the .... Age-related mechanisms of amino acid signalling in skeletal muscle. This project aims to increase our understanding of the role of glycine receptor-mediated signalling and its metabolism in the amino acid sensing capacity of mTORC1, a key enzyme regulating muscle protein synthesis. Ageing is associated with a progressive decline in skeletal muscle mass, weakness, and impaired regeneration after injury. Impaired anabolic signalling after food intake has been proposed as a key contributor, yet the metabolic pathways responsible for nutrient sensing and regulation of protein synthesis remain unresolved. The project will assess defective amino acid sensing and protein synthesis in old mammals, identifying the role of glycine signalling in these processes. The project expects to underpin development of muscle-specific modulators of muscle homeostasis with broad relevance to Australia’s ageing population.
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    Funded Activity

    ARC Future Fellowships - Grant ID: FT120100397

    Funder
    Australian Research Council
    Funding Amount
    $818,856.00
    Summary
    Roles of the kynurenine pathway in physiological and pathological brain function. This project will aim to study the metabolism of the essential amino acid tryptophan in the brain and its involvement in diseases including multiple sclerosis and brain tumours.
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    Funded Activity

    ARC Future Fellowships - Grant ID: FT100100546

    Funder
    Australian Research Council
    Funding Amount
    $803,217.00
    Summary
    Unraveling the role of N-acetyl-aspartate in normal brain function and disease. The purpose of this project is to define the role of the predominating brain chemical N-acetyl-aspartate for normal nerve cell function and as toxic agent causing neurological illness and severe mental health problems. Findings of this research will enhance the design of novel therapies involving pharmacological and genetic treatment.
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    Funded Activity

    Discovery Projects - Grant ID: DP150102883

    Funder
    Australian Research Council
    Funding Amount
    $560,000.00
    Summary
    A novel family of amino acid transporters in Apicomplexan parasites. Apicomplexan parasites are single celled organisms that are the causative agents of major diseases in livestock and humans. However, the basic biochemistry of these intracellular parasites is poorly understood, and there are limited treatments available for the diseases these parasites cause. The project hypothesis is that a novel family of proteins that are unique to apicomplexan parasites play a key role in the uptake of esse .... A novel family of amino acid transporters in Apicomplexan parasites. Apicomplexan parasites are single celled organisms that are the causative agents of major diseases in livestock and humans. However, the basic biochemistry of these intracellular parasites is poorly understood, and there are limited treatments available for the diseases these parasites cause. The project hypothesis is that a novel family of proteins that are unique to apicomplexan parasites play a key role in the uptake of essential nutrients (amino acids) into these organisms. This project aims to use a combination of genetic, biochemical and physiological methods to understand the function of these proteins, the role(s) that they play in apicomplexan biology, and their importance for parasite survival.
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    Active Funded Activity

    Discovery Projects - Grant ID: DP200103530

    Funder
    Australian Research Council
    Funding Amount
    $437,420.00
    Summary
    The “New” Biochemistry of Polyamines: When Metabolic Pathways Collide. Basic biochemistry and the metabolic regulation of proliferation remain as the fundamental building blocks of knowledge in cell biology that have enabled breakthrough advances in biology and medicine. Polyamines are unique and ubiquitous low-Mr amines that play vital roles in many biological processes, including proliferation, DNA/RNA synthesis, etc. This proposal will mechanistically dissect the "new" biochemistry of polyami .... The “New” Biochemistry of Polyamines: When Metabolic Pathways Collide. Basic biochemistry and the metabolic regulation of proliferation remain as the fundamental building blocks of knowledge in cell biology that have enabled breakthrough advances in biology and medicine. Polyamines are unique and ubiquitous low-Mr amines that play vital roles in many biological processes, including proliferation, DNA/RNA synthesis, etc. This proposal will mechanistically dissect the "new" biochemistry of polyamines, as we have discovered that polyamines are regulated by iron at 2-major levels, involving >10-key polyamine pathway proteins. This proposal represents first-in-field studies specifically designed to dissect mechanisms involved in this relationship. Our Central Hypothesis is that iron regulates polyamine metabolism.
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    Funded Activity

    ARC Future Fellowships - Grant ID: FT120100039

    Funder
    Australian Research Council
    Funding Amount
    $707,628.00
    Summary
    Defining the cellular impacts of protein aggregation in neurodegenerative disease with an aggreomics platform. The brain disease Huntington’s is caused by abnormally shaped proteins that assemble into toxic clusters. This project will design new bioprobes to track how these clusters form and cause damage to cells. This strategy will also provide new opportunities for discovering novel therapeutic targets.
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