Isolation of isoform-specific binding proteins (Affimers) by phage display using negative selection

Anna Ah-San Tang, Christian Tiede, David J Hughes, Michael J McPherson, Darren C Tomlinson

Research output: Contribution to journalArticlepeer-review

22 Citations (Scopus)
2 Downloads (Pure)


Some 30 years after its discovery, phage display remains one of the most widely used methods of in vitro selection. Initially developed to revolutionize the generation of therapeutic antibodies, phage display is now the first choice for screening artificial binding proteins. Artificial binding proteins can be used as reagents to study protein-protein interactions, target posttranslational modifications, and distinguish between homologous proteins. They can also be used as research and affinity reagents, for diagnostic purposes, and as therapeutics. However, the ability to identify isoform-specific reagents remains highly challenging. We describe an adapted phage display protocol using an artificial binding protein (Affimer) for the selection of isoform-selective binding proteins.

Original languageEnglish
Article numbereaan0868
Number of pages12
JournalScience Signaling
Issue number505
Publication statusPublished - 14 Nov 2017


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