| Literature DB >> 26367875 |
Vanessa Siegmund1, Stefan Schmelz2, Stephan Dickgiesser1, Jan Beck1, Aileen Ebenig1, Heiko Fittler1, Holm Frauendorf3, Birgit Piater4, Ulrich A K Betz4, Olga Avrutina1, Andrea Scrima2, Hans-Lothar Fuchsbauer5, Harald Kolmar6.
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.Entities:
Keywords: antibodies; bioconjugation; protein engineering; site-specific ligation; transglutaminase
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Year: 2015 PMID: 26367875 DOI: 10.1002/anie.201504851
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336