Options
Locked by Design: A Conformationally Constrained Transglutaminase Tag Enables Efficient Site-Specific Conjugation
ISSN
1521-3773
1433-7851
Date Issued
2015
Author(s)
Siegmund, Vanessa
Schmelz, Stefan
Dickgiesser, Stephan
Beck, Jan
Ebenig, Aileen
Fittler, Heiko
Piater, Birgit
Betz, Ulrich A. K.
Avrutina, Olga
Scrima, Andrea
Fuchsbauer, Hans-Lothar
Kolmar, Harald
DOI
10.1002/anie.201504851
Abstract
Based on the crystal structure of a natural protein substrate for microbial transglutaminase, an enzyme that catalyzes protein crosslinking, a recognition motif for site-specific conjugation was rationally designed. Conformationally locked by an intramolecular disulfide bond, this structural mimic of a native conjugation site ensured efficient conjugation of a reporter cargo to the therapeutic monoclonal antibody cetuximab without erosion of its binding properties.