| Literature DB >> 26633100 |
Giang K T Nguyen1, Antony Kam1, Shining Loo1, Anna E Jansson1, Lucy X Pan1, James P Tam1.
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.Mesh:
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Year: 2015 PMID: 26633100 DOI: 10.1021/jacs.5b11014
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419