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Research Topic : lipid bilayers
Scheme : NHMRC Project Grants
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  • Funded Activity

    Functional And Structural Studies Of A Glycosyltransferase Essential For Complex Glycolipid Biosynthesis In Mycobacteria

    Funder
    National Health and Medical Research Council
    Funding Amount
    $508,838.00
    Summary
    Tuberculosis (TB) kills more than three million people each year while the causative bacterial species, Mycobacterium tuberculosis, infects one-third of the entire human population. An alarmingly high rate of TB exists in Australia's indigenous population. This proposal aims to identify and characterise essential processes involved in synthesis of the outer coat of the bacterium which are potential targets for new drugs for the treatment of this devastating disease.
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    Funded Activity

    Development Of Bacterial Mechanosensitive Channels As Nanodevices In Liposome Systems For Targeted Drug Delivery

    Funder
    National Health and Medical Research Council
    Funding Amount
    $502,341.00
    Summary
    Liposomes are among the most advanced mainstream particulate drug carriers in modern medicine. They vary in complexity, but in their most basic form consist of naturally occurring phospholipid vesicles, capable of encapsulating a wide range of drugs. Such liposomes provide a high degree of biocompatibility and a physical barrier that protects the drug cargo from degradative enzymes in the patient. Furthermore, liposomes provide an effective, non-toxic method to solubilise hydrophobic drugs and a .... Liposomes are among the most advanced mainstream particulate drug carriers in modern medicine. They vary in complexity, but in their most basic form consist of naturally occurring phospholipid vesicles, capable of encapsulating a wide range of drugs. Such liposomes provide a high degree of biocompatibility and a physical barrier that protects the drug cargo from degradative enzymes in the patient. Furthermore, liposomes provide an effective, non-toxic method to solubilise hydrophobic drugs and administer potent and even highly toxic drugs such as the anthracyclines, Doxorubicin and Daunorubicin (clinically approved anti-cancer treatments), Amphotericin B (fungal disease therapy) and Taxol (cancer therapy).The focus of this project is to incorporate nanovalves into these drug delivery systems, in the form of bacterial mechanosensitive (MS) channels, to facilitate the controlled and rapid release of encapsulated drugs at targeted tumours or disease tissues. The successful completion of this project represents a significant advance on existing liposomal drug delivery systems because MS channels open and release the drug into or onto the target cell immediately following liposome binding. Liposomal drug delivery systems offer the additional advantages that they concentrate the drug inside the target tissue, thereby increasing its efficacy; reduce the exposure of healthy cells to toxic drugs; and increase safety to patients through loading site-specific drugs into site-directed liposomes. Specifically this project will develop: 1. Liposome formulations in which the MS channels are closed, but poised to open upon binding to the target cell. 2. Customised MS channels designed to optimize controlled release. 3. Structural information that will assist in the treatment of channelopathies linked to MS channels, i.e. diseases resulting from defects in MS ion channel function (e.g. muscular dystrophy, cardiac arrhythmias, autosomal-dominant polycystic kidney disease).
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    Funded Activity

    Mechanosensitive Channels: Antimicrobials, Channelopathies And Nanovalves For Drug Delivery

    Funder
    National Health and Medical Research Council
    Funding Amount
    $673,953.00
    Summary
    Liposomal drug delivery systems (LDDS) are one of the most advanced particulate drug carriers in modern medicine. The ultimate goal of this project is to optimize a nanotechnology approach for improved control of therapeutic drug delivery for chemotherapy. The approach is using bacterial mechanosensitive channel MscL designed to act as a molecular nanovalve for localised drug release.
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    Funded Activity

    A Novel Patch-fluorimetry Technique For Investigating Structural Changes During Gating Of Mechanosensitive Ion Channnels

    Funder
    National Health and Medical Research Council
    Funding Amount
    $387,018.00
    Summary
    Membrane proteins, especially membrane channels play an important role in regulating the flow of substances across the cell. Dysfunction in these channels can lead to a variety of diseases. Thus approximately 60% of drug development is targeted against such proteins. In our research, we are looking at membrane channels found in bacteria. Understanding the function of these channels will help us develop novel anti-bacterial agents. It will also aid to understand a role of ion channels in disease.
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    Funded Activity

    The Role Of Seipin In Lipid Metabolism And Adipogenesis

    Funder
    National Health and Medical Research Council
    Funding Amount
    $397,749.00
    Summary
    The prevalence of obesity and its related disorders has reached an alarming level in Australia and other developed countries. Obesity is characterized by accumulation of fully-differentiated adipocytes loaded with lipid droplets (LDs). Therefore, understanding the cellular dynamics of LDs and the molecular mechanisms of adipogenesis (adipocyte differentiation) is of crucial importance in our battle against obesity. Our proposed study will help undertand the mechnisams of obesity.
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    Funded Activity

    Lipoprotein Metabolism And Mutations Of The APOB Gene Causing Familial Hypobetalipoproteinaemia

    Funder
    National Health and Medical Research Council
    Funding Amount
    $396,179.00
    Summary
    Cardiovascular disease is an increasing problem in Australia, however, the cause of atherosclerosis is incompletely understood. A protein, known as apolipoprotein (apo) B, plays a central role in lipoprotein metabolism. Elevated levels of apoB are characteristic of many forms of hypercholestrolaemia. Familial combined hyperlipidaemia and polygenic hypercholesterolaemia are two common inherited disorders of lipoprotein metabolism that are characterised by elevated apoB levels in the blood and ear .... Cardiovascular disease is an increasing problem in Australia, however, the cause of atherosclerosis is incompletely understood. A protein, known as apolipoprotein (apo) B, plays a central role in lipoprotein metabolism. Elevated levels of apoB are characteristic of many forms of hypercholestrolaemia. Familial combined hyperlipidaemia and polygenic hypercholesterolaemia are two common inherited disorders of lipoprotein metabolism that are characterised by elevated apoB levels in the blood and early atherosclerosis. In contrast, familial hypobetalipoproteinemia is a rare inherited disorder of lipoprotein metabolism characterised by very low levels of cholesterol and apoB in the blood and resistance to atherosclerosis and cardiovascular disease. The focus of this research project is to explore the regulation of apoB metabolism using individuals from unique families with familial hypobetalipoproteinaemia. First, we will determine and characterise the alterations in the APOB gene causing the low cholesterol levels in families with familial hypobetalipoproteinaemia. Second, we will determine if these apoB alterations affect the production and-or clearance of blood fats, or lipoproteins in affected individuals, when compared to controls, by performing metabolic studies. The proposed human in vivo metabolic studies will lead to a better understanding of the mechanism(s) involved in the assembly, secretion, transport, and clearance of plasma apoB-containing lipoproteins. Furthermore, these studies may reveal new protective mechanisms and potentially aid in the development of strategies to suppress over-production of apoB-containing lipoproteins in reciprocal conditions such as familial combined hyperlipidaemia or polygenic hypercholesterolaemia.
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    Funded Activity

    Identifying A Novel Role For Pigment Epithelium-derived Factor In Obesity-related Metabolic Dysfunction

    Funder
    National Health and Medical Research Council
    Funding Amount
    $361,637.00
    Summary
    Obesity is an important factor contributing to insulin resistance and type 2 diabetes; however, the factors linking these disorders are not well defined. A protein called PEDF is elevated in obesity and type 2 diabetes. This project will examine how PEDF causes insulin resistance and whether blocking PEDF's actions prevents insulin resistance. Successful completion of this project may lead to therapeutics that reduce the risk of developing type 2 diabetes.
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    Funded Activity

    The Role Of Endothelial Lipase In High Density Lipoprotein Metabolism

    Funder
    National Health and Medical Research Council
    Funding Amount
    $130,550.00
    Summary
    Atherosclerosis is a major cause of death and disability in Australia. A high level of blood cholesterol increases the risk of developing atherosclerosis. This increase in risk is caused by the cholesterol that is carried in low density lipoproteins (LDL). However, not all cholesterol is bad. A proportion of the cholesterol in blood is carried in high density lipoproteins (HDL), which are powerful protectors against atherosclerosis. As not all HDL protect equally well against atherosclerosis, it .... Atherosclerosis is a major cause of death and disability in Australia. A high level of blood cholesterol increases the risk of developing atherosclerosis. This increase in risk is caused by the cholesterol that is carried in low density lipoproteins (LDL). However, not all cholesterol is bad. A proportion of the cholesterol in blood is carried in high density lipoproteins (HDL), which are powerful protectors against atherosclerosis. As not all HDL protect equally well against atherosclerosis, it is important to know how blood levels of HDL are regulated. In 1999 a new enzyme called endothelial lipase was discovered. Endothelial lipase dramatically decreases HDL levels in mice. The reason why this happens is not known. The main aims of this project are to work out how endothelial lipase decreases HDL levels and whether it decreases the levels of all HDL equally or whether it preferentially decreases the levels of certain types of HDL. The outcome of this project will establish how endothelial lipase affects the ability of HDL to protect against atherosclerosis in humans.
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    Funded Activity

    Niemann Pick Disease Type C And Intracellular Sterol Trafficking

    Funder
    National Health and Medical Research Council
    Funding Amount
    $317,741.00
    Summary
    Abnormal distribution of cellular cholesterol causes Nieman Pick Disease type C (NP-C), and is also strongly associated with common neurodegenerative diseases such as Alzheimer's disease. We aim to understand the molecular mechanisms by which cholesterol is sorted and transported in the cell. Our results may help develop effective therapeutic strategies against NP-C, Alzheimers' disease and other cholesterol related disorders.
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    Funded Activity

    The Role Of Lycopene Supplementation In The Management Of Asthma

    Funder
    National Health and Medical Research Council
    Funding Amount
    $332,875.00
    Summary
    Asthma is a significant and increasing health problem for Australia and is now listed as a National Health Priority Area. There is immense community interest in dietary factors affecting asthma. This project examines the potential for dietary carotenoids to be used to manage asthma. Carotenoids are antioxidants that are found in orange and red fruits and vegetables, such as tomatoes, carrots and mangoes. Research suggests that dietary carotenoids may be protective against asthma symptoms and -or .... Asthma is a significant and increasing health problem for Australia and is now listed as a National Health Priority Area. There is immense community interest in dietary factors affecting asthma. This project examines the potential for dietary carotenoids to be used to manage asthma. Carotenoids are antioxidants that are found in orange and red fruits and vegetables, such as tomatoes, carrots and mangoes. Research suggests that dietary carotenoids may be protective against asthma symptoms and -or onset. It is also likely that increasing intake of carotenoid-rich foods may be more effective than taking dietary supplements, as the key nutrients or combination of nutrients may not be known. This project will examine whether carotenoids such as lycopene can reduce the tendency of asthmatic airways to overreact to common triggers. It also investigates whether carotenoids can be used to prevent or reduce the severity of asthma attacks. The project will determine whether tomato juice or lycopene capsules are more effective in this role. This work will provide the necessary information to develop a large trial testing the ability of carotenoids to improve quality of life for people with asthma. While there is evidence to suggest that carotenoids may be helpful in asthma, the data to date is inconclusive. This study provides a scientific approach to evaluating the potential for carotenoids to be used as a treatment for asthma.
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