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A Protocol for Phage Display and Affinity Selection Using Recombinant Protein Baits
Published on: February 16, 2014
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Isolation of isoform-specific binding proteins (Affimers) by phage display using negative selection
Anna Ah-San Tang1,2, Christian Tiede1,2, David J Hughes3
1School of Molecular and Cellular Biology, Faculty of Biological Science, University of Leeds, Leeds LS2 9JT, UK.
Science Signaling
|November 16, 2017
Summary
Phage display technology enables the selection of artificial binding proteins. An adapted protocol using Affimers successfully identifies isoform-specific binding proteins, overcoming a key challenge.
Area of Science:
- Biotechnology
- Molecular Biology
- Protein Engineering
Background:
- Phage display is a powerful in vitro selection technique widely used for generating binding proteins.
- Artificial binding proteins have diverse applications, including diagnostics, therapeutics, and research reagents.
- Selecting isoform-specific binding proteins using current methods remains a significant challenge.
Purpose of the Study:
- To adapt phage display for the selection of highly specific binding proteins.
- To develop a method for identifying isoform-selective reagents.
- To overcome limitations in current protein selection strategies.
Main Methods:
- Utilized an adapted phage display protocol.
- Employed artificial binding proteins known as Affimers.
- Focused on the selection of isoform-specific binding proteins.
Main Results:
- Successfully adapted the phage display protocol for enhanced protein selection.
- Demonstrated the capability of Affimers in selecting isoform-specific binding proteins.
- Overcame the challenge of identifying isoform-selective reagents.
Conclusions:
- The adapted phage display protocol is effective for selecting isoform-specific binding proteins.
- Affimer technology provides a viable approach for generating targeted protein reagents.
- This method advances the development of specific reagents for research and therapeutic applications.

