Back to Search
Start Over
Fabrication of cysteine-modified antibodies with Fc-specific conjugation for covalent and oriented immobilization of native antibodies.
- Source :
-
International journal of biological macromolecules [Int J Biol Macromol] 2024 Sep; Vol. 276 (Pt 2), pp. 133962. Date of Electronic Publication: 2024 Jul 17. - Publication Year :
- 2024
-
Abstract
- Covalent and oriented immobilization of antibodies (Abs) can substantially improve the sensitivity and stability of solid-phase immunoassays. By modifying the natural Abs with functional groups that provide unique handles for further conjugation, Abs could be immobilized onto the solid matrices with uniform orientation. Herein, an effective approach for Fc-specific modification of Abs was developed for the oriented and covalent immobilization of Abs. Twelve photoreactive Z-domain variants, incorporated with a photoactivable probe (p-benzoyl-L-phenylalanine, Bpa) at different positions and carrying a C-terminal Cys-tag (i.e. Z <subscript>Bpa</subscript> -Cys variants), were individually constructed and produced in Escherichia coli and tested for photo-cross-linking to various IgGs. The different Z <subscript>Bpa</subscript> -Cys variants demonstrated large differences in photo-conjugation efficiency for the tested IgGs. The conjugation efficiencies of <superscript>17th</superscript> Z <subscript>Bpa</subscript> -Cys ranged from 90 % to nearly 100 % for rabbit IgG and mouse IgG <subscript>2a</subscript> , IgG <subscript>2b</subscript> and IgG <subscript>3</subscript> . Other variants, including <superscript>5th</superscript> Z <subscript>Bpa</subscript> -Cys, <superscript>18th</superscript> Z <subscript>Bpa</subscript> -Cys, <superscript>32th</superscript> Z <subscript>Bpa</subscript> -Cys, and <superscript>35th</superscript> Z <subscript>Bpa</subscript> -Cys, also displayed conjugation efficiencies of 61 %-83 % for mouse IgG <subscript>1</subscript> , IgG <subscript>2a</subscript> and IgG <subscript>3</subscript> . Subsequently, the photo-modified Abs, namely IgG-Cys conjugates, were covalently immobilized onto a maleimide group-functionalized solid-phase carrier on the basis of the reaction of sulfhydryl and maleimide. Thus, a generic platform for the controlled and oriented immobilization of Abs was developed, and the efficacy and potential of the proposed approach for sensitive immunoassays was demonstrated by detecting human α-fetoprotein.<br />Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2024 Elsevier B.V. All rights reserved.)
- Subjects :
- Animals
Mice
Rabbits
Phenylalanine chemistry
Phenylalanine analogs & derivatives
Immunoassay methods
Escherichia coli
Antibodies chemistry
Antibodies immunology
Cysteine chemistry
Immunoglobulin G chemistry
Immunoglobulin G immunology
Immunoglobulin Fc Fragments chemistry
Antibodies, Immobilized chemistry
Antibodies, Immobilized immunology
Subjects
Details
- Language :
- English
- ISSN :
- 1879-0003
- Volume :
- 276
- Issue :
- Pt 2
- Database :
- MEDLINE
- Journal :
- International journal of biological macromolecules
- Publication Type :
- Academic Journal
- Accession number :
- 39029833
- Full Text :
- https://doi.org/10.1016/j.ijbiomac.2024.133962