Abstract
Macrocyclization is a valuable tool for drug design and protein engineering. Although various methods have been developed to prepare macrocycles, a general and efficient strategy is needed. Here we report a highly efficient method using butelase 1 to macrocyclize peptides and proteins ranging in sizes from 26 to >200 residues. We achieved cyclizations that are 20,000 times faster than sortase A, the most widely used ligase for protein cyclization. The reactions completed within minutes with up to 95% yields.
Original language | English |
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Pages (from-to) | 15398-15401 |
Journal | Journal of the American Chemical Society |
Volume | 137 |
Issue number | 49 |
Publication status | Published - 3 Dec 2015 |