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. Author manuscript; available in PMC: 2021 Apr 13.
Published in final edited form as: Cancer Cell. 2020 Apr 13;37(4):431–442. doi: 10.1016/j.ccell.2020.03.014

Figure 3A-D. New frontiers for drug development.

Figure 3A-D.

(A) Isoform-selective inhibitors bind to an individual protein isoform within the cell. (B) Antibody drug conjugates bind to cell surface antigens and are internalized into the cell where they release a cytotoxic payload to induce cell death. (C) Proteolysis Targeting Chimeras (PROTACs) bind both mutant proteins and E3 ubiquitin ligase, facilitating proteasomal degradation of the target. (D) Protein refolders enable mutant proteins to regain wildtype conformation and activity.