Sarah L. Perry

The paper develops a graphene device for high-temperature crystallography to study enzymatic reactivity across temperature ranges, revealing how transition state ensembles relate to catalytic rates.

The paper uses molecular dynamics simulations to identify a unifying mechanism for excipient-mediated protein thermal stability based on shape complementarity between proteins and solvents.

This paper introduces CapSACIN, a computational framework to study virus-excipient interactions, showing it effectively models PPV stability and excipient effects.

This paper describes a scalable microfluidic device for automated X-ray crystallography that enables efficient and damage-free crystal mounting for protein structure analysis.