Woo‐Chan Ahn

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.