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. 2023:2681:83-97.
doi: 10.1007/978-1-0716-3279-6_6.

Phage Display of Bovine Ultralong CDRH3

Affiliations

Phage Display of Bovine Ultralong CDRH3

Callum Joyce et al. Methods Mol Biol. 2023.

Abstract

Phage display is an in vitro technique used in the discovery of monoclonal antibodies that has been used successfully in the discovery of both camelid VHH and shark variable new antigen receptor domains (VNAR). Bovines also contain a unique "ultralong CDRH3" with a conserved structural motif, comprising a knob domain and β-stalk. When removed from the antibody scaffold, either the entire ultralong CDRH3 or the knob domain alone, is typically capable of binding an antigen, to produce antibody fragments that are smaller than both VHH and VNAR. By extracting immune material from bovine animals and specifically amplifying knob domain DNA sequences by PCR, knob domain sequences can be cloned into a phagemid vector producing knob domain phage libraries. Target-specific knob domains can be enriched by panning the libraries against an antigen of interest. Phage display of knob domains exploits the link between phage genotype and phenotype and could prove to be a high throughput method to discover target-specific knob domains, helping to explore the pharmacological properties of this unique antibody fragment.

Keywords: Antibody display; Antibody engineering; Bovine ultra-long CDR3H antibodies; Phage display; Stalk-knob.

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References

    1. Alfaleh M, Alsaab H, Mahmoud A et al (2020) Phage display derived monoclonal antibodies: from bench to bedside. Front Immunol 11:1986. https://doi.org/10.3389/fimmu.2020.01986 - DOI - PubMed - PMC
    1. McCafferty J, Griffiths AD, Winter G, Chiswell DJ (1990) Phage antibodies: filamentous phage displaying antibody variable domains. Nature 348(6301):552–554 - DOI - PubMed
    1. Romao E, Morales-Yanez F, Hu Y et al (2017) Identification of useful nanobodies by phage display of immune single domain libraries derived from camelid heavy chain antibodies. Curr Pharm Des 22(43):6500–6518 - DOI
    1. Berens S, Wylie D, Lopez O (1997) Use of a single VH family and long CDR3s in the variable region of cattle Ig heavy chains. Int Immunol 9(1):189–199 - DOI - PubMed
    1. Wang F, Ekiert DC, Ahmad I et al (2013) Reshaping antibody diversity. Cell 153(6):1379–1393 - DOI - PubMed - PMC

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