Gustavo Avelar Molina

A rapid, automation-friendly, cell-free and purification-free pipeline for binding and kinetic characterisation of de novo designed binders with high quality standardised per-design data

This paper presents a rapid, automation-friendly pipeline for characterizing de novo protein binders without cell culture or purification, achieving binding affinity and kinetics in three days.

Interrelationship of substrate crystallinity, enzyme binding strength, and cellulase activity

This study examines the relationship between substrate crystallinity, enzyme binding strength, and cellulase activity, revealing a linear free energy relationship with varying slopes linked to substrate crystallinity.