Using structural biology to understand programmed cell death

Using structural biology to understand programmed cell death

Project details

Apoptosis is the principle pathway that targets cells for programmed death and is required for removal of faulty cells, for example due to viral infection or cancer. Defective cell death can contribute to disease in various settings including cancers, heart attack, stroke or degenerative disease (Moldoveanu and Czabotar, Cold Spring Harbour Perpec Biol 2020 vol 12).  

We are interested in understanding how the pro-apoptotic proteins Bax and Bak, members of the BCL-2 protein family, promote apoptosis. To understand this we will characterise 3D structures of Bax using X-ray crystallography and CryoEM. In addition we will characterise binding of ligands to Bax using a combination of structural and biophysical techniques.  

The project will suit students interested in protein crystallography, structural biology, drug discovery and protein-ligand interactions. 

 

About our research group

The Czabotar lab is situated in the Structural Biology division. Our research focuses on using X-ray crystallography, CryoEM and other biophysical techniques to understand the processes involved in targeted cell death (eg Czabotar, Cell 2013 152:519-31). We aim to exploit high resolution structural information obtained by crystal structures to guide development of novel therapies for diseases characterized by cell death and to understand resistance mechanisms to drugs targeting the family members eg venetoclax (Birkinshaw Nature Communication 2018 vol 10 p2835).  

 

Email supervisors

 

Researchers:

Dr Michelle Miller
Dr
Michelle
Miller
Structural Biology division
Dr Richard Birkinshaw profile shot
Dr
Richard
Birkinshaw
Structural Biology division

Project Type: