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Research Topic : Membrane Protiens
Field of Research : Cellular Immunology
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  • Researchers (34)
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  • Funded Activity

    How Does T Cell Receptor Signaling Begin?

    Funder
    National Health and Medical Research Council
    Funding Amount
    $318,768.00
    Summary
    The initial step of T cell activation of how the external ligand binding is translated to an increase of receptor phosphorylation at the cytoplasmic side is remain poorly understood. It is believed that the loss of immune recognition in cancer and over reactivity in auto-immune diseases are caused by abnormality of this transmembrane signalling transduction. Clarification of this molecular machinery can provide a molecular basis of those diseases and guidelines of more effective therapies.
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    Funded Activity

    Structure And Composition Of The Pre-T Cell Receptor-CD3 Complex

    Funder
    National Health and Medical Research Council
    Funding Amount
    $307,946.00
    Summary
    In order to recognize a wide variety of pathogens, humans produce many different T cell receptors (TCRs) by the process of gene-rearrangement. However, gene-rearrangement may not always lead to a functioning TCR. We are studying the pre-TCR protein that is responsible for monitoring the success of gene-rearrangement and is thus essential for the formation of a robust immune system. Understanding pre-TCR function will lead to new treatments for immune related diseases.
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    Funded Activity

    The Structure And Composition Of The T-Cell Receptor-CD3 Complex

    Funder
    National Health and Medical Research Council
    Funding Amount
    $419,180.00
    Summary
    My research will use cutting edge imaging techniques to provide a fundamental advance in our understanding of how foreign viruses and pathogens trigger the immune system. Gaining a greater understanding of these central events will facilitate the design of novel therapies to treat immune associated disorders such as transplant rejection, autoimmune disease and some cancers.
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    Funded Activity

    Linkage Infrastructure, Equipment And Facilities - Grant ID: LE160100097

    Funder
    Australian Research Council
    Funding Amount
    $675,000.00
    Summary
    An Automated Protein Nano-Crystallisation Facility. An automated protein nano-crystallisation facility: The project aims to establish a high throughput protein nanocrystallisation and imaging facility for protein crystallography. Protein crystallography is an important field of biological research, however there are many proteins, such as integral membrane proteins and transient molecular complexes that are more challenging to crystallise. The facility aims to use state-of-the-art imaging and c .... An Automated Protein Nano-Crystallisation Facility. An automated protein nano-crystallisation facility: The project aims to establish a high throughput protein nanocrystallisation and imaging facility for protein crystallography. Protein crystallography is an important field of biological research, however there are many proteins, such as integral membrane proteins and transient molecular complexes that are more challenging to crystallise. The facility aims to use state-of-the-art imaging and crystallisation techniques, including second order nonlinear imaging of chiral crystals (SONICC) imaging and lipid cubic phase approaches, to enable structural studies to be undertaken on challenging proteins. This information is often used for the rational development of therapeutics. The facility would support cutting-edge biological research In Australia.
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    Active Funded Activity

    Discovery Projects - Grant ID: DP220102288

    Funder
    Australian Research Council
    Funding Amount
    $597,830.00
    Summary
    A novel axis of cooperation between innate and adaptive immunity. The project aims to understand how two molecular components of the immune system, Complement and MHC, cooperate to protect the host. Further, these two molecules mediate trogocytosis, a little-studied form of intercellular communication, between two major immune cell types: dendritic cells and B cells. The project will be multidisciplinary, applying high-end microscopy, biochemistry, cell biology and immunology techniques. Person .... A novel axis of cooperation between innate and adaptive immunity. The project aims to understand how two molecular components of the immune system, Complement and MHC, cooperate to protect the host. Further, these two molecules mediate trogocytosis, a little-studied form of intercellular communication, between two major immune cell types: dendritic cells and B cells. The project will be multidisciplinary, applying high-end microscopy, biochemistry, cell biology and immunology techniques. Personnel will be trained in cutting-edge techniques. The project will expand knowledge on basic immunology and cell-cell cooperation. It will generate intellectual property for the biotechnology sector to develop new commercial products that might improve the health of humans and also animals of economic importance.
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    Funded Activity

    Analysis Of Antigen Receptor Sharing By T And B Lymphocytes

    Funder
    National Health and Medical Research Council
    Funding Amount
    $540,356.00
    Summary
    To survive an infection the immune system must rapidly expand the number of immune cells that have pathogen-specific receptors that recognise, and therefore specifically combat, the infection. This normally occurs through proliferation of the immune cells. We have found that in addition to proliferation, the number of cells with these receptors can be increased by a process of receptor transfer between cells. This grant aims to further advance our understanding of this novel phenomenon.
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    Active Funded Activity

    Discovery Early Career Researcher Award - Grant ID: DE220100830

    Funder
    Australian Research Council
    Funding Amount
    $464,928.00
    Summary
    Elucidating the genesis of MAIT cell-mediated immunity. T cells develop in the thymus and proceed to survey our body probing molecules that signal if anything is abnormal. A specialised subset of T cells, mucosal associated invariant T (MAIT) cells are crucial in detecting microbial molecules and infection, yet their numbers vary widely between individuals. A key problem is that the factors controlling their development and function are poorly understood. This proposal aims to decode this critic .... Elucidating the genesis of MAIT cell-mediated immunity. T cells develop in the thymus and proceed to survey our body probing molecules that signal if anything is abnormal. A specialised subset of T cells, mucosal associated invariant T (MAIT) cells are crucial in detecting microbial molecules and infection, yet their numbers vary widely between individuals. A key problem is that the factors controlling their development and function are poorly understood. This proposal aims to decode this critical issue in MAIT cell biology, using innovative tools to investigate the molecular basis underpinning their development in the thymus. This work will provide vital, fundamental discoveries into how MAIT cells are produced and regulated, as we ultimately wish to harness MAIT cells to improve human health.
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    Funded Activity

    Antigen Receptor Sharing By Lymphocytes During An Immune Response

    Funder
    National Health and Medical Research Council
    Funding Amount
    $286,328.00
    Summary
    A successful immune response relies on the ability of immune cells to quickly mount a specific offensive against invading foreign pathogens like bacteria or viruses. The specificity of this offensive is governed by receptors that can recognise pathogens. To survive an infection the immune system must rapidly expand the number of immune cells that have receptors that recognise, and can therefore specifically combat, the infection. The underlying theory of immunology, the clonal selection theory, .... A successful immune response relies on the ability of immune cells to quickly mount a specific offensive against invading foreign pathogens like bacteria or viruses. The specificity of this offensive is governed by receptors that can recognise pathogens. To survive an infection the immune system must rapidly expand the number of immune cells that have receptors that recognise, and can therefore specifically combat, the infection. The underlying theory of immunology, the clonal selection theory, states that this expansion is mediated by the proliferation of immune cells selected on the basis of expressing a pathogen specific receptor. We hypothesise that in addition to this proliferation the immune system may also expand the number of immune cells expressing pathogen-specific receptors by transferring these receptors between cells by a means of cell-membrane sharing. Indeed, we have evidence that this does occur both in the test tube and in animals and can function to amplify the number of immune cells that can specifically recognise a pathogen and thereby help with immune response development. This grant aims to further advance our understanding of this novel phenomenon.
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    Funded Activity

    Discovery Early Career Researcher Award - Grant ID: DE130100251

    Funder
    Australian Research Council
    Funding Amount
    $375,000.00
    Summary
    Biophysical mechanisms regulating early T cell signalling events. T cell activation in response to foreign pathogens or cancer cells requires a complex set of protein interactions which must be controlled in space and time. This project will use new microscopy methods with single-molecule sensitivity to determine how the cell membrane and protein clustering regulate these interactions.
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    Funded Activity

    Australian Laureate Fellowships - Grant ID: FL160100049

    Funder
    Australian Research Council
    Funding Amount
    $2,915,738.00
    Summary
    A molecular investigation into immune function. A molecular investigation into immune function. The project aims to understand how key immune recognition events enable immunity. This project would use a multidisciplinary approach empowered by technological innovations, including the latest advances in atomic and molecular imaging. This research is expected to identify new approaches for the biotechnology industry.
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