| Literature DB >> 28771896 |
Philipp R Spycher1, Christian A Amann1, Jöri E Wehrmüller1, David R Hurwitz1, Olivier Kreis1, Daniel Messmer2, Andreas Ritler1,3, Andreas Küchler2, Alain Blanc1, Martin Béhé1, Peter Walde2, Roger Schibli1,4.
Abstract
Microbial transglutaminase (MTG) was stably solid-phase immobilized on glass microbeads by using a second-generation dendronized polymer. Immobilized MTG enabled the efficient generation of site-specifically conjugated proteins, including antibody fragments, as well as whole antibodies through distinct glutamines and, unprecedentedly, also through lysines with various bifunctional substrates with defined stoichiometries. With this method, we generated dual, site-specifically modified antibodies comprising a fluorescent probe and a metal chelator for radiolabeling-a strategy anticipated to design antibodies for imaging and simultaneous therapy. Furthermore, we provide evidence that immobilized MTG features higher siteselectivity than soluble MTG.Entities:
Keywords: antibodies; bioconjugation; immobilization; site-specific modification; transglutaminase
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Year: 2017 PMID: 28771896 DOI: 10.1002/cbic.201700188
Source DB: PubMed Journal: Chembiochem ISSN: 1439-4227 Impact factor: 3.164