Candice S. Klug

This study investigates how receptor phosphorylation and membrane lipids cooperatively control arrestin activation, identifying key phospho-motifs and lipid interactions.

This study compares the membrane-binding properties of arrestin-2 and arrestin-3 using biophysical and cell-based methods, revealing distinct lipid interaction mechanisms and activation dynamics.

The paper develops a high-sensitivity stopped-flow EPR system for studying millisecond protein conformational dynamics, demonstrating its use on T4 lysozyme and β2 adrenergic receptor.

This paper improves EPR sensitivity for small aqueous biological samples using optimized dielectric resonators and multi-channel cells.