Ka Yang
Junior PIka_yang@szbl.ac.cn
Educational background&Work experience
2026-Present Junior PI, Shenzhen Bay Laboratory,Research field
“Hard-to-drug” proteins lack clear ligandable sites, dynamic regulatory mechanisms, and effective intervention tools, representing a major bottleneck in innovative drug discovery. Focusing on the question of "how to discover small-molecule-regulatable functional sites and intervene in protein homeostasis at the proteomic scale," the research group has developed a research strategy of "site discovery—mechanism elucidation—chemical modulation." By applying technologies including high-throughput chemical proteomics, targeted protein degradation, and bioinformatics, the group focuses on identifying and validating new drug targets/sites, exploring the ligandability of undruggable targets, and discovering bioactive small molecules for the treatment of disease.