Description
Cells constantly monitor nutrients and energy levels to decide whether to grow, divide or recycle their contents. A major control point for this decision-making occurs at the lysosome, where large protein complexes sense nutrient availability and regulate mTORC1, a master pathway controlling cell growth, autophagy and metabolism. When this system is disrupted, it can contribute to cancer, metabolic disease and other disorders.
This project will investigate how lysosome-associated signalling complexes assemble and control mTORC1 activity. Students will contribute to a broader research program using structural biology, cryo-EM, protein biochemistry, mass spectrometry, computational modelling and live-cell biosensors to understand how these molecular machines work. Depending on the project stage, an Honours or PhD student could focus on protein complex purification, cryo-EM sample preparation, structural analysis, biochemical reconstitution, or the development and testing of biosensors that report signalling activity in living cells. The project is suited to students interested in structural biology, cell signalling, metabolism and molecular mechanisms of disease.
Essential criteria:
Minimum entry requirements can be found here: https://www.monash.edu/admissions/entry-requirements/minimum
Keywords
cryo-EM, lysosomes, mTORC1, TORC1, nutrient sensing, cell growth, metabolism, autophagy, structural biology, protein complexes, signalling complexes, membrane biology, cell signalling, cryo-ET, cross-linking mass spectrometry, live-cell imaging, FRET biosensors, protein engineering, biosensors, computational modelling, cancer biology, metabolic regulation
School
Biomedicine Discovery Institute (School of Biomedical Sciences) » Biochemistry and Molecular Biology
Available options
PhD/Doctorate
Honours
Time commitment
Full-time
Physical location
Monash Clayton Campus
