JobDescription
Ice-binding proteins (IBPs) protect against freeze damage in polar regions by keeping the nucleation and growth of ice crystals in check. How this works exactly is not yet known. This is because we currently lack designer ice-binders to unravel and utilize the structure-function relations underlying activity. In this project you will combine computational tools for protein engineering (de novo protein design, folding) with biochemical and structural biology techniques (protein expression, structure elucidation, activity assays) to bridge this knowledge gap. You will engineer IBPs de novo. You will express and study promising designs to elucidate the relation between IBP structure, composition and function. Through collaborations within the group and (inter)nationally, you will study how your designer IBPs with optimized and customized activity interact with ice and may be exploited for cardiac regenerative medicine.
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