Proteins form up to 25% of our diet. The first step in protein absorption is the digestion of protein into smaller units called peptides and amino acids. Both components are subsequently taken up by specialised cells in the wall of the intestine. In this project we plan to study how protein absorption occurs at the surface of these intestinal cells and investigate why this process fails in malabsorption syndromes, where the uptake of amino acids is impaired.
The Potential Benefit Of Resistant Starch On Zinc Retention And Its Potential For Utilisation In Infants At Risk Of Zinc Deficiency.
Funder
National Health and Medical Research Council
Funding Amount
$101,991.00
Summary
Resistant starch (RS) can promote absorption of minerals such as calcium and magnesium from the large intestine. As zinc deficiency in children from the developing world remains a major public health issue, we will use a rodent model to determine if RS can improve zinc absorption in growing rats with preceeding zinc deficiency. In parallel we will also determine whether infants, who are most vulnerable to the effects of zinc deficiency, have the gut bacteria required to utilise the potential and ....Resistant starch (RS) can promote absorption of minerals such as calcium and magnesium from the large intestine. As zinc deficiency in children from the developing world remains a major public health issue, we will use a rodent model to determine if RS can improve zinc absorption in growing rats with preceeding zinc deficiency. In parallel we will also determine whether infants, who are most vulnerable to the effects of zinc deficiency, have the gut bacteria required to utilise the potential and known health benefits of RS.Read moreRead less
Involvement Of Interstitial Cells Of Cajal In The Pathogenesis Of Diabetic Gastroparesis
Funder
National Health and Medical Research Council
Funding Amount
$386,104.00
Summary
Diabetics commonly suffer from gastrointestinal symptoms such as bloating and nausea. We have preliminary evidence that interstitial cells of Cajal (ICC), which are essential for normal gut motility, are particularly vunerable to damage in diabetes. The goal of this study is to determine how the loss of ICC in diabetes leads to delayed gastric emptying. Our overall aim is to identify potential therapeutic targets for improved treatment of diabetes-related gastrointestinal motility disorders.
Role Of Hsp40 And Hsp70 In Huntingtin Misfolding, Oligomerization And Inclusion Assembly
Funder
National Health and Medical Research Council
Funding Amount
$590,103.00
Summary
Huntington disease results from a mutation that causes the Htt protein to become abnormally sticky and form toxic clusters in neurons. Cells have natural defences to clustering with proteins called chaperones, which are exciting therapeutic targets. This project will examine how chaperones defend against toxic Htt clustering with cutting-edge imaging technologies. The knowledge gained will aid in designing therapeutic strategies that stimulate the defence processes and suppress the clusters.
Developing Novel Molecules That Target Hormone Receptors As An Alternative Cancer Therapy
Funder
National Health and Medical Research Council
Funding Amount
$459,867.00
Summary
A promising class of cancer drugs target heat shock protein 90 (Hsp90) and prevent Hsp90 from maintaining its ~100 proteins involved in cell growth. However, all current Hsp90 chemotherapeutics non-selectively target proteins maintained by Hsp90, and induce a cell rescue mechanism involving Hsp70. We describe the development of a novel molecule that will selectively control cell growth and prevent cell rescue via a unique Hsp90 regulated mechanism.
Understanding Age-related Protein Aggregation. The Mechanism Of Cataract And Its Prevention
Funder
National Health and Medical Research Council
Funding Amount
$709,333.00
Summary
Cataract arises from clouding of the eye lens due to the aggregation of crystallin proteins whose high concentration and close packing facilitate lens transparency. This proposal will investigate crystallin structure and interactions to understand the reasons for cataract formation and its prevention via the design of aggregation inhibitors. The results will facilitate the development of drugs to prevent cataract and other related protein aggregation diseases, e.g. Alzheimer’s and Parkinson’s.
Directed Molecular Evolution Of G Protein-coupled Receptors For Stable And Functional Expression In Escherichia Coli
Funder
National Health and Medical Research Council
Funding Amount
$383,479.00
Summary
Approximately half of all prescription drugs on the market act on G protein coupled receptors (GPCRs). The mechanisms underlying GPCR function are mainly unknown due to a lack of structural information. No solved structures exist for any of the estimated 800 human GPCRs, making it difficult to design new drugs. By applying advanced protein engineering techniques I aim to produce human GPCRs in bacteria to ultimately acquire structural information, which will enable novel drug development.