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Scheme : Project Grants
Research Topic : Protein Regulation
Australian State/Territory : NSW
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  • Funded Activity

    Structural And Functional Analysis Of A Cancer-linked Co-regulator Complex

    Funder
    National Health and Medical Research Council
    Funding Amount
    $729,571.00
    Summary
    We seek to understand the mechanisms by which genes are switched on and off throughout our lifetime. A number of multi-component protein machines are involved in this process but their make-up and mechanism of action is not understood. We will investigate the structure and function of one of these machines that has been strongly linked to cancer.
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    Funded Activity

    Discovery And Mechanisms Of Host Cell Factors In HIV Uncoating

    Funder
    National Health and Medical Research Council
    Funding Amount
    $635,098.00
    Summary
    HIV entry into the host cell involves release of its capsid, a protein shell protecting the viral genome. The capsid hijacks host proteins to cloak itself from cellular defenses while the cell has evolved sensors that can block viral infection. This proposal aims to discover proteins involved in this arms race between host and virus and decipher how they control capsid disassembly. This insight will help design new drugs against HIV infection and new ways to deliver genes for gene therapies.
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    Funded Activity

    Prion-like Behaviour In Immunity: Super-sized Signalling Platforms?

    Funder
    National Health and Medical Research Council
    Funding Amount
    $611,995.00
    Summary
    Prions have been mostly associated with pathologies but recent discoveries show that prion-like behaviour may be beneficial, enhancing our immune response for example. To test this, we want to systematically explore all human proteins involved in the defence against pathogens, find new prion-like trends and probe their role in the innate immune response.
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    Funded Activity

    Lipid Modulation Of Glycine Transporters

    Funder
    National Health and Medical Research Council
    Funding Amount
    $368,659.00
    Summary
    Many drugs modulate the function of proteins imbedded in cell membranes. Extensive research has been undertaken to better understand drug interactions with these proteins to improve drug therapies, but there has been relatively little progress in understanding the role of the cell membrane. This project will investigate how the cell membrane influences protein function and then use this information to develop novel drugs for the treatment of neurological disorders.
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    Funded Activity

    Genomic Analysis Of DNA Binding And Gene Regulation By The Chromatin Remodelling Factor UBF

    Funder
    National Health and Medical Research Council
    Funding Amount
    $624,254.00
    Summary
    Synthesis of ribosomes, the cellular protein synthetic machinery, is the major anabolic event of a growing cell and is frequently dysregulated during disease such as cancer. This grant will examine a protein termed UBF that we think plays an important role in orchestrating the cellular response to dysregulated ribosome biogenesis. By understanding how UBF functions we hope to uncover novel therapeutic approaches to treat diseases associated with ribosome stress .
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    Funded Activity

    The Structural Basis For Glutamate Transporter Function

    Funder
    National Health and Medical Research Council
    Funding Amount
    $373,144.00
    Summary
    Glutamate transporters are vacuum cleaners in the brain that suck the neurotransmitter glutamate into cells. When the glutamate vacuum breaks down or becomes blocked, glutamate levels outside cells increase, leading to cell death in the brain. This process underlies the damage in many brain diseases including Alzheimer’s disease and stroke. The aim of this project is to understand the mechanism of the glutamate vacuum cleaner so we can develop therapeutics to fix it when it breaks down.
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    Funded Activity

    H2A.Z Acetylation: Deregulation Of Enhancer Activity And 3D Chromatin In Prostate Cancer

    Funder
    National Health and Medical Research Council
    Funding Amount
    $859,350.00
    Summary
    DNA is not linear but packaged in the cell nucleus in a three-dimensional (3D) structure in such a way that distal regulatory regions can interact to control gene expression. Our new data suggests that a chemical modification of the histone variant H2A.Z plays a critical role in the formation of the 3D chromatin structure. This project is aimed to dissect the role of H2A.Z in prescribing 3D structure, which will provide a more precise understanding of gene deregulation in cancer.
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    Funded Activity

    Deciphering The Transcriptional Program That Instructs Lymphatic Endothelial Cell Fate.

    Funder
    National Health and Medical Research Council
    Funding Amount
    $541,950.00
    Summary
    Lymphatic vessels are essential to maintain fluid balance in most tissues of the human body. Further the lymphatic vasculature plays a central role during cancer and contributes to tumour metastasis. Despite this integral function in health and disease little is known about the molecular programs that coordinate gene expression to build a functional vasculature. This research project will address this gap in our knowledge and will open up new therapeutic avenues for lymphatic vascular disorders
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    Funded Activity

    Regulation Of Ribosomal RNA Gene Chromatin During Malignant Transformation.

    Funder
    National Health and Medical Research Council
    Funding Amount
    $882,486.00
    Summary
    The overarching goal of this proposal is to determine the molecular basis for tumour cell dependence on activated ribosomal RNA gene repeats (rDNA). Our working model posits that rDNA repeats become activated through changes in rDNA chromatin structure that include increased binding of the RNA Polymerase I transcription factor UBF.
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    Funded Activity

    Mechanistic And Functional Analysis Of The Id4 Proto-oncogene In Breast And Ovarian Cancer

    Funder
    National Health and Medical Research Council
    Funding Amount
    $693,983.00
    Summary
    Cancer arises through damage to normal regulatory processes in cells. Understanding these damaged processes is essential to implement personalized medicine. This proposal explores the role of the proto-oncogene ID4 in the closely related cancers triple negative breast cancer and serous ovarian cancer. This research may lead to the development of new therapeutic strategies or the refinement of existing strategies for these poor prognosis cancers.
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