Selectivity is a key obstacle in drug development. A new study describes how “peptide stapling,” a technique for making peptide α-helices more potent and cell permeable, allows the design of MCL-1 inhibitors with extraordinary selectivity.
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Kritzer, J. Magic bullets in nature's arsenal. Nat Chem Biol 6, 566–567 (2010). https://doi.org/10.1038/nchembio.407
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DOI: https://doi.org/10.1038/nchembio.407
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