Eui‐Jeon Woo

This paper redesigns an Fc-binding peptide to enable multivalent antibody assembly without altering the IgG scaffold, showing enhanced stability and functional utility.

This study identifies how cFP binds ToxRS in V. vulnificus to activate virulence genes by stabilizing the ToxR-ToxS heterodimer and enhancing promoter binding.

This paper develops an AI-guided method to design protein inhibitors that modulate FAD-GDH redox output, demonstrating their effectiveness in reducing GDH-mediated redox activity.

This paper designs AI-driven nanobinders targeting the TSLPR-IL-7R heterodimer interface to suppress type 2 inflammatory signaling, showing that geometric mimicry of the native cytokine is more effective than affinity alone.

This paper designs a potent Wnt surrogate specific for Fzd7 subtype members, showing strong binding affinity and functional activity in organoid formation and hair regeneration.