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Research Topic : cell population dynamics
Status : Declined
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Biochemistry and Cell Biology (3)
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  • Funded Activity

    Discovery Projects - Grant ID: DP220102089

    Funder
    Australian Research Council
    Funding Amount
    $454,560.00
    Summary
    Investigating Wnt signaling during human nephron commitment and patterning. Aims: To use gene edited stem cell lines that display cell location, identity and cell state to map human kidney tissue formation in the laboratory. By monitoring how each cell responds to those around it across time and space, we will for the first time map the formation of kidney tissue in the dish. Significance: Understanding how stem cells form a tissue will help us to improve and control the process. This is key to .... Investigating Wnt signaling during human nephron commitment and patterning. Aims: To use gene edited stem cell lines that display cell location, identity and cell state to map human kidney tissue formation in the laboratory. By monitoring how each cell responds to those around it across time and space, we will for the first time map the formation of kidney tissue in the dish. Significance: Understanding how stem cells form a tissue will help us to improve and control the process. This is key to advancing tissue engineering. Expected outcomes: The proposal will pioneer state-of-the-art imaging, gene editing and machine learning approaches, generating models of human development that are currently unavailable. Benefits: This understanding will guide the development of novel approaches to tissue engineering.
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    Funded Activity

    Discovery Early Career Researcher Award - Grant ID: DE160100293

    Funder
    Australian Research Council
    Funding Amount
    $372,000.00
    Summary
    Cracking the phosphoinositide code. This project seeks to determine how protein interactions with membrane lipids regulate recruitment to cellular organelles, providing new insight into the complex pathways of cellular homeostasis. Controlling the distribution of proteins within cells is critical for cell signalling and membrane trafficking. This is orchestrated by the interaction of specific protein modules with lipids on the surface of different organelles. The phox homology (PX) domain is a l .... Cracking the phosphoinositide code. This project seeks to determine how protein interactions with membrane lipids regulate recruitment to cellular organelles, providing new insight into the complex pathways of cellular homeostasis. Controlling the distribution of proteins within cells is critical for cell signalling and membrane trafficking. This is orchestrated by the interaction of specific protein modules with lipids on the surface of different organelles. The phox homology (PX) domain is a lipid-binding module found in numerous proteins essential for normal cell trafficking and homeostasis, and perturbed in many conditions including immune dysfunction and cancer. This project plans to investigate molecular determinants of PX-lipid association, generating knowledge about protein-membrane interactions required for cellular function. These insights may underpin future drug design.
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    Funded Activity

    Discovery Early Career Researcher Award - Grant ID: DE160101535

    Funder
    Australian Research Council
    Funding Amount
    $363,000.00
    Summary
    Ancient genomics of Western Australian taxa to inform conservation management. The project aims to apply genomic approaches to infer the genetic health and evolutionary history of three threatened, iconic Western Australian taxa: black cockatoos, ghost bats and woylies. Genomic data provide a powerful lens through which to study species, but the applications of genomic techniques in conservation biology have been sparse. Effective restoration and conservation initiatives require an understanding .... Ancient genomics of Western Australian taxa to inform conservation management. The project aims to apply genomic approaches to infer the genetic health and evolutionary history of three threatened, iconic Western Australian taxa: black cockatoos, ghost bats and woylies. Genomic data provide a powerful lens through which to study species, but the applications of genomic techniques in conservation biology have been sparse. Effective restoration and conservation initiatives require an understanding of species' former population sizes, connectivity and biodiversity. The project seeks to elucidate the population genetic, phylogenetic, and conservation genetic parameters of the three species at the genomic level using DNA isolated from modern and ancient sources (eg museum skins and fossils). The information gained may inform conservation efforts for some of Australia’s endangered biota.
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    Funded Activity

    Discovery Early Career Researcher Award - Grant ID: DE240100793

    Funder
    Australian Research Council
    Funding Amount
    $463,180.00
    Summary
    Unraveling a new cytokine working model in immune cell exhaustion. This project will investigate a novel paradigm of how a key messenger protein can be sensed by fundamental immune cells, preventing their ‘exhaustion’. Immune cell exhaustion is a fundamental mechanism to maintain the internal homeostasis of vertebrates. However, it is often hijacked by pathogens to dampen the defensive capacity of the immune system. And this specific messenger protein is the only known soluble factor that can d .... Unraveling a new cytokine working model in immune cell exhaustion. This project will investigate a novel paradigm of how a key messenger protein can be sensed by fundamental immune cells, preventing their ‘exhaustion’. Immune cell exhaustion is a fundamental mechanism to maintain the internal homeostasis of vertebrates. However, it is often hijacked by pathogens to dampen the defensive capacity of the immune system. And this specific messenger protein is the only known soluble factor that can deliver ‘anti-exhaustion’ signals to immune cells. This study will advance basic knowledge in biochemistry and immunology by combining interdisciplinary and cutting-edge approaches. The expected outcomes include the developing new scientific theories and identifying novel molecular basis of biological processes.
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    Funded Activity

    Australian Laureate Fellowships - Grant ID: FL160100170

    Funder
    Australian Research Council
    Funding Amount
    $2,887,531.00
    Summary
    Scaling in biology: size control at the cell, organelle and organism level. This project aims to decipher the universal mechanisms that coordinate growth with division and thereby dictate the size of the cell. It would investigate this question from the triangulating perspective of evolution using yeast and animal models. It plans to interrogate the complex sub-networks that govern cell size using novel genome-scale reagent sets for systematic genetics and other approaches. It would integrate th .... Scaling in biology: size control at the cell, organelle and organism level. This project aims to decipher the universal mechanisms that coordinate growth with division and thereby dictate the size of the cell. It would investigate this question from the triangulating perspective of evolution using yeast and animal models. It plans to interrogate the complex sub-networks that govern cell size using novel genome-scale reagent sets for systematic genetics and other approaches. It would integrate this data in predictive mathematical models of size control that illuminate how the cell processes size-related information, and how size mechanisms evolve to impact form and function in biology. This research is expected to have commercial applications in biotechnology processes and bioengineering.
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