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| Publications [#260736] of Ashutosh Chilkoti
search scholar.google.com.Papers Published
- Bellucci, JJ; Bhattacharyya, J; Chilkoti, A, A noncanonical function of sortase enables site-specific conjugation of small molecules to lysine residues in proteins.,
Angewandte Chemie (International ed. in English), vol. 54 no. 2
(January, 2015),
pp. 441-445, ISSN 1433-7851 [doi]
(last updated on 2026/01/15)
Abstract: We provide the first demonstration that isopeptide ligation, a noncanonical activity of the enzyme sortase A, can be used to modify recombinant proteins. This reaction was used in vitro to conjugate small molecules to a peptide, an engineered targeting protein, and a full-length monoclonal antibody with an exquisite level of control over the site of conjugation. Attachment to the protein substrate occurred exclusively through isopeptide bonds at a lysine ε-amino group within a specific amino acid sequence. This reaction allows more than one molecule to be site-specifically conjugated to a protein at internal sites, thereby overcoming significant limitations of the canonical native peptide ligation reaction catalyzed by sortase A. Our method provides a unique chemical ligation procedure that is orthogonal to existing methods, supplying a new method to site-specifically modify lysine residues that will be a valuable addition to the protein conjugation toolbox.
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