Nature Biotechnology
19, 75 - 78 (2001)
doi:10.1038/83567
A helper phage to improve single-chain antibody presentation in phage displaySusanne Rondot1, 5, Joachim Koch2, 5, Frank Breitling3
& Stefan Dübel41
Molekulargenetisches Labor Prof. Raue, Friedrich-Ebert-Anlage 28, 69117 Heidelberg, Germany. 2
Forschungsstelle Hantaviren der Heidelberger Akademie der Wissenschaften, Im Neuenheimer Feld 230, 69120 Heidelberg, Germany. 3
Abt. Genomanalyse, Deutsches Krebsforschungszentrum, Im Neuenheimer Feld 280, 69120 Heidelberg, Germany. 4
Molekulare Genetik, Universität Heidelberg, Im Neuenheimer Feld 230, 69120 Heidelberg, Germany. 5
The first two authors contributed equally to this work.
Correspondence should be addressed to Stefan Dübel sd@uni-hd.deWe show here that the number of single-chain antibody fragments (scFv) presented on filamentous phage particles generated with antibody display phagemids can be increased by more than two orders of magnitude by using a newly developed helper phage (hyperphage). Hyperphage have a wild-type pIII phenotype and are therefore able to infect F+ Escherichia coli cells with high efficiency; however, their lack of a functional pIII gene means that the phagemid-encoded pIII−antibody fusion is the sole source of pIII in phage assembly. This results in an considerable increase in the fraction of phage particles carrying an antibody fragment on their surface. Antigen-binding activity was increased about 400-fold by enforced oligovalent antibody display on every phage particle. When used for packaging a universal human scFv library, hyperphage improved the specific enrichment factor obtained when panning on tetanus toxin. After two panning rounds, more than 50% of the phage were found to bind to the antigen, compared to 3% when conventional M13KO7 helper phage was used. Thus, hyperphage is particularly useful in stoichiometric situations, when there is little chance that a single phage will locate the desired antigen.
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