Speaker
Roman Hillig
Description
The selenoprotein GPX4 is a potential cancer drug target. Inhibitors covalently target the active site selenocysteine. Co-crystallization with covalent inhibitors initially failed, most likely due to heterogenous covalent modification. A mass spec-based approach to monitor cysteine modification, together with a surface cysteine mutation, enabled the structure determination of GPX4 with the covalent inhibitor ML162 and opens the path to further inhibitor co-complex structures of this drug target.
Primary author
Roman Hillig