Literature DB >> 31332760

Site-Specific Photocrosslinking to Immunoglobulin G Using Photoreactive Antibody-Binding Domains.

Fabiana Zappala1, Andrew Tsourkas2.   

Abstract

The high specificity and strong binding affinity of antibodies, most commonly immunoglobulin G (IgG), have led to their use in a wide range of research, diagnostic and therapeutic applications. Many of these applications require the antibody to be labeled with additional chemical or biological moieties. Here, we describe a method for the rapid and site-specific labeling of nearly any "off-the-shelf" IgG. Our method utilizes small photoreactive antibody-binding domains (pAbBDs) that are produced by modifying the IgG-binding domains of Protein A and Protein G with the unnatural amino acid benzoylphenylalanine (BPA). The pAbBDs are covalently linked to IgG heavy chains upon exposure to ultraviolet light. Fusion of pAbBDs to a given protein of interest or conjugation of pAbBDs with drugs, fluorophores, and/or other chemical moieties, enables the facile production of a diverse range of antibody conjugates.

Entities:  

Keywords:  Antibody conjugates; Antibody labeling; Bioconjugation; Immunoglobulin G; Photocrosslinking; Site-specific modification; Unnatural amino acids

Mesh:

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Year:  2019        PMID: 31332760     DOI: 10.1007/978-1-4939-9654-4_18

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  2 in total

Review 1.  Protein scaffolds: antibody alternatives for cancer diagnosis and therapy.

Authors:  Renli Luo; Hongguang Liu; Zhen Cheng
Journal:  RSC Chem Biol       Date:  2022-05-25

2.  Rapid Production of Bispecific Antibodies from Off-the-Shelf IgGs with High Yield and Purity.

Authors:  Linghan Mei; Fabiana Zappala; Andrew Tsourkas
Journal:  Bioconjug Chem       Date:  2021-12-12       Impact factor: 6.069

  2 in total

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