We report here a generally applicable method for the selective covalent attachment of a reporter molecule to a replicating entity that allows one to obtain specific binders from a single round of library screening. We show that selective biotinylation of phage particles displaying a binder to any given target can be achieved by application of a coupled enzyme reaction on the surface of the target-binding phage particles that includes a peroxidase, an oxidase and a catalase. Due to the covalent linkage of biotin together with the tight and stable interaction of biotin with streptavidin, very stringent wash conditions for removal of nonspecific binders can be applied. The method termed 3CARD (triple catalytic reporter deposition) was successfully applied to single-round screening of a phage display library of camelid single-domain antibodies against three different target proteins. © 2013 © The Author 2014. Published by Oxford University Press. All rights reserved.
CITATION STYLE
Maaß, A., Heiseler, T., Maaß, F., Fritz, J., Hofmeyer, T., Glotzbach, B., … Kolmar, H. (2014). A general strategy for antibody library screening via conversion of transient target binding into permanent reporter deposition. Protein Engineering, Design and Selection, 27(2), 41–47. https://doi.org/10.1093/protein/gzt060
Mendeley helps you to discover research relevant for your work.