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Molecular Proteomics

Using quantitative proteomics to study the molecular function of secreted factors and extracellular vesicles in cancer, cardiometabolic disease and normal physiology

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Latest Achievements

Helen Amelia Hains Fellow

President, Australia and New Zealand Society of Extracellular Vesicles

Ludwig Institute for Cancer Research Excellence Medal

International Protein Society Hans Neurath Outstanding Promise Award

ROYAN International Research Award on Reproductive Biomedicine

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Associate Professor David Greening Laboratory Head
We use a multi-disciplinary approach to understand the molecular function of extracellular vesicles incorporating proteomics, cell biology, molecular biology, and physiology, with the goal of identifying new deliverable therapeutic targets.

 

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About the Molecular Proteomics laboratory

The Molecular Proteomics laboratory is focused on understanding the molecular function of nano-sized biological extracellular vesicles and how their intercellular signalling is important in normal physiology and pathologies including cancer and cardiometabolic disease with the goal of identifying new deliverable therapeutic targets. The advanced-nano approaches developed in our lab have identified novel regulators of secretome (cell-derived secreted factors) and extracellular vesicle biology and have utilised this knowledge for commercial and translational potential.

Extracellular vesicles are sophisticated signalling mediators, transporting select RNA and protein cargo. As secreted vesicles they have the capacity to enable intercellular communication and have become the focus of exponentially growing interest, both to study their functions and to understand ways to use them in the development of minimally invasive diagnostics. Importantly, extracellular vesicles are released into biological fluids including blood, urine, uterine fluid, and protect their cargo against degradation and denaturation in the extracellular environment.

We are particularly interested in studying dynamic changes in proteins and their post-translational modifications, and understanding how extracellular vesicles mediate function to ultimately shape cellular physiology. We primarily focus on cardiometabolic disease (fibrotic processes during myocardial infarction and hypertension), implantation biology and molecular events associated with implantation and receptivity (embryo-endometrial cross-talk) and cancer progression. It is crucial to define extracellular vesicles and understand the molecular mechanisms of their signalling and reprogramming to develop better approaches to investigate the many functions of cell communication, including in normal physiology and how they contribute to disease. This knowledge will lead to design of nano-carriers for the targeted and selective delivery to target organs/cells, define mechanisms of delivery and reprogramming of target cells, and development of novel therapeutics targeted to intercellular signalling.

We use a multi-disciplinary approach to understand the molecular function of extracellular vesicles incorporating proteomics, cell biology, molecular biology, nanomaterials, nanobiotechnology, regenerative cell biology, physiology, and experts in molecular therapies with the goal of identifying new deliverable therapeutic targets and facilitate effective engineered nanoparticles for next generation cell-free therapies.

Positions available

We offer projects in each of these areas, and a specific topic will be selected to cater for the interests and skills of a candidate. A prospective student will be a part of a successful multidisciplinary research team of molecular biologists, cell biologists, proteomics, nanomaterials, extracellular vesicles, and clinical scientists, and will gain experience in quantitative omics technologies (including proteomics), cardiovascular disease, cell biology, molecular biology and biochemistry. Contact us for more information...

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With the rising number of Australians affected by diabetes, heart disease and stroke, the need for research is more critical than ever.

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