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Preparation and Identification of a Single Domain Antibody Specific for Adenovirus Vectors and Its Application to the Immunoaffinity Purification of Adenoviruses

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Journal AMB Express
Date 2022 Jun 20
PMID 35723787
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Abstract

Adenovirus belongs to the family of Adenoviridae. As a vaccine carrier, it has high safety and stimulates the body to produce cellular immunity and humoral immunity. This study prepared an adenoviral vector-specific single-domain antibody for use in adenovirus identification and purification. We successfully constructed a single domain antibody phage display library with a capacity of 1.8 × 10 by immunizing and cloning the VHH gene from Bactrian camel. After the second round of biopanning, clones specific for adenovirus were screened using phage ELISA. Twenty-two positive clones were obtained, and two clones with the highest binding affinity from ELISA were selected and named sdAb 5 and sdAb 31 for further application. The recombinant single-domain antibody was solublely expressed in E. coli and specifically bound to adenoviruses rAd26, ChAd63 and HAd5 in ELISA and live cell immunofluorescence assays. We established an effective method for immunoaffinity purification of adenovirus by immobilizing the single domain antibody to Sepharose beads, and it may be used to selectively capture adenoviruses from cell culture medium. The preparation of the adenovirus-specific single-domain antibody lays a foundation for the one-step immunoaffinity purification and identification of adenoviruses.

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References
1.
Zhu F, Jin P, Zhu T, Wang W, Ye H, Pan H . Safety and Immunogenicity of a Recombinant Adenovirus Type-5-Vectored Coronavirus Disease 2019 (COVID-19) Vaccine With a Homologous Prime-Boost Regimen in Healthy Participants Aged ≥6 Years: A Randomized, Double-Blind, Placebo-Controlled, Phase 2b.... Clin Infect Dis. 2021; 75(1):e783-e791. PMC: 8522421. DOI: 10.1093/cid/ciab845. View

2.
Beghein E, Gettemans J . Nanobody Technology: A Versatile Toolkit for Microscopic Imaging, Protein-Protein Interaction Analysis, and Protein Function Exploration. Front Immunol. 2017; 8:771. PMC: 5495861. DOI: 10.3389/fimmu.2017.00771. View

3.
TRENTIN J, Yabe Y, Taylor G . The quest for human cancer viruses. Science. 1962; 137(3533):835-41. DOI: 10.1126/science.137.3533.835. View

4.
Vincke C, Loris R, Saerens D, Martinez-Rodriguez S, Muyldermans S, Conrath K . General strategy to humanize a camelid single-domain antibody and identification of a universal humanized nanobody scaffold. J Biol Chem. 2008; 284(5):3273-3284. DOI: 10.1074/jbc.M806889200. View

5.
Lafaye P, Li T . Use of camel single-domain antibodies for the diagnosis and treatment of zoonotic diseases. Comp Immunol Microbiol Infect Dis. 2018; 60:17-22. PMC: 7112682. DOI: 10.1016/j.cimid.2018.09.009. View