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Australian State/Territory : QLD
Research Topic : Protein characterisation
Socio-Economic Objective : Infectious Diseases
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Biochemistry and Cell Biology (3)
Protein Trafficking (3)
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Characterisation of Biological Macromolecules (1)
Industrial Biotechnology Diagnostics (incl. Biosensors) (1)
Industrial Molecular Engineering of Nucleic Acids and Proteins (1)
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  • Funded Activity

    Discovery Projects - Grant ID: DP110103920

    Funder
    Australian Research Council
    Funding Amount
    $315,000.00
    Summary
    SNARE-mediated perforin and cytokine release in natural killer cells. Cytotoxic cells release toxic granules and cytokine messengers to kill pathogen infected and cancerous cells and to mount immune responses. This project will investigate different SNARE molecules that regulate the secretion of perforin from granules and cytokines from other carriers, assisting in the understanding of complex but essential cellular pathways.
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    Funded Activity

    Discovery Projects - Grant ID: DP150100364

    Funder
    Australian Research Council
    Funding Amount
    $370,600.00
    Summary
    Formation of the Chlamydial Inclusion Requires Host Trafficking Pathways. Using cellular and biochemical approaches this project aims to examine the membrane trafficking pathways hijacked by the pathogen Chlamydia and to define the key components of these pathways. Chlamydia are obligate intracellular pathogens responsible for a range of human and animal diseases. In order to survive within the host cell, the pathogen hijacks the host's membrane trafficking pathways to engineer an intracellular .... Formation of the Chlamydial Inclusion Requires Host Trafficking Pathways. Using cellular and biochemical approaches this project aims to examine the membrane trafficking pathways hijacked by the pathogen Chlamydia and to define the key components of these pathways. Chlamydia are obligate intracellular pathogens responsible for a range of human and animal diseases. In order to survive within the host cell, the pathogen hijacks the host's membrane trafficking pathways to engineer an intracellular niche called an inclusion. In addition to providing a permissive environment, this strategy also shields the pathogen from the host's immune system.
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    Funded Activity

    Linkage Projects - Grant ID: LP100200504

    Funder
    Australian Research Council
    Funding Amount
    $225,000.00
    Summary
    Next generation dengue diagnostics. The 2009 dengue epidemic was widespread and the largest in North Queensland for 50 years. The outbreak was not quickly contained despite an extensive education program and a mosquito control taskforce. All four types of Dengue were detected, greatly increasing the chance of more severe complications such as Dengue haemorrhagic fever and Dengue shock syndrome. This project will improve our knowledge of Dengue proteins used in tests to diagnose the virus. The ne .... Next generation dengue diagnostics. The 2009 dengue epidemic was widespread and the largest in North Queensland for 50 years. The outbreak was not quickly contained despite an extensive education program and a mosquito control taskforce. All four types of Dengue were detected, greatly increasing the chance of more severe complications such as Dengue haemorrhagic fever and Dengue shock syndrome. This project will improve our knowledge of Dengue proteins used in tests to diagnose the virus. The new knowledge will be used to develop an easy to use test to diagnose Dengue infection early, rapidly and accurately. Effective diagnosis of Dengue will then allow timely implementation of intervention strategies (mosquito control, public advice, isolation and care).
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    Funded Activity

    ARC Future Fellowships - Grant ID: FT110100831

    Funder
    Australian Research Council
    Funding Amount
    $822,556.00
    Summary
    Regulation of human immunodeficiency virus type 1 (HIV-1) replication by viral and cellular proteins. Using a mouse model, human cells will be treated with a very powerful antiviral protein using a gene therapy approach so as to block the human immunodeficiency virus (HIV) from growing. By learning how this antiviral protein works, this project will assist in the development of new strategies to treat HIV infection.
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    Showing 1-4 of 4 Funded Activites

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