Joshua S. Sharp

This study applies radical protein footprinting to mammalian whole blood, identifying disease-associated conformational changes in proteins from T2DM mice.

This paper introduces a novel method using radical carbohydrate footprinting to identify glycan-protein interactions and map binding interfaces by analyzing oxidation patterns of oligosaccharides.

This study identifies the fondaparinux binding sites on JR-FL gp120 using hydroxyl radical footprinting and docking, showing two binding regions: the V3 loop and the N- and C-termini.