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Updated: Sep 17, 2025

A Protocol for Phage Display and Affinity Selection Using Recombinant Protein Baits
Published on: February 16, 2014
The first thermophilic phage display system
Piotr M Skowron1, Ireneusz Sobolewski1, Katarzyna Adamowicz1
1Department of Molecular Biotechnology, Faculty of Chemistry, University of Gdansk, Wita Stwosza 63, 80-308, Gdansk, Poland.
Abstract:
Phage display technology is a powerful technique that allows to expose any peptide fused to a bacteriophage coat protein on the surface of the virion. However, the phage display systems have limitations that impair their applications in microbiology and biotechnology. We present the construction of the first thermophilic phage display system, including 'mosaic' system, and provide examples of its biotechnological usefulness. The system relies on TP-84 bacteriophage, infecting Geobacillus stearothermophilus, with proliferation temperature up to 73°C, and developing only in the lytic mode, which allows liberating virion with any attached peptide. TP-84 has a large capsid, tolerates changes in the capsid proteins arrangement and develops in the thermophilic host, preventing recombinant protein aggregation in the cytoplasm. Furthermore, we introduce 'affinity coupling' functionalized bionanoparticle system, allowing attachment of theoretically any size proteins or even non-proteinous ligands onto TP-84 capsid, overcoming genome/capsid size limitations. The system provides technology for generation of novel types thermostable, biodegradable biomaterials. Moreover, the duplicated major capsid protein phage was constructed, forming the first thermophilic phage gene expression system. Upon a replacement of the engineered TP84_12 gene copy by a gene to be expressed, high level recombinant proteins expression can be achieved. This versatile phage display system should be useful in many microbiological approaches, overcoming the drawbacks of previous systems.
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