Official Project Description
Cryogenic electron microscopy has revolutionized the field of molecular biology.
It has revealed the structures of thousands of previously uncharacterised proteins, enabling the development of new therapeutics for every kind of human disease.
A crucial step in the preparation of proteins for study in this method involves the rapid cooling and vitrification of dissolved protein in liquid ethane.
Despite the ubiquity of this technique, its effects on molecular structure are not well understood, leaving important implications for the field of molecular biophysics.
In this project we will explicitly simulate the vitrification process to understand how it perturbs molecular structures-teaching us what kinds of structures are preserved during cooling and which ones are lost.
This will enable the transformation of cryogenic electron microscopy into a quantitative biophysical tool, letting us develop drugs more quickly and accurately for all diseases.