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Development of recombinant secondary antibody mimics (rSAMs) for immunoassays through genetic fusion of monomeric alkaline phosphatase with antibody binders.
- Source :
-
International journal of biological macromolecules [Int J Biol Macromol] 2023 Nov 01; Vol. 251, pp. 126299. Date of Electronic Publication: 2023 Aug 11. - Publication Year :
- 2023
-
Abstract
- In conventional immunoassays, a secondary antibody is used to amplify the signal generated by the binding of the primary antibody to the target analyte. Due to concerns regarding animal use and cost-inefficiency of secondary antibody productions, there is a significant demand for the development of recombinant secondary antibody mimics (rSAMs). Here, we developed rSAMs using a signal-generating enzyme, monomeric alkaline phosphatase (mALP), and antibody-binders, including monomeric streptavidin (mSA2) and mouse IgG1- or rabbit IgG-binding nanobodies (MG1Nb or RNb). The mALP-MG1Nb, mALP-RNb, and mALP-mSA2 were genetically constructed and produced in large quantities using bacterial overexpression systems, which reduced manufacturing costs and time without the use of animals. Each rSAM exhibited high and selective binding to its respective primary antibody, generating linear band signals corresponding to the amounts of target analytes in western blots. The rSAMs also successfully generated sigmoidal signal curves that increased as the sample concentration increased. Moreover, they generated stronger signals than conventional ALP-conjugated secondary antibodies and SA, particularly in the medium to high sample concentration range, in both indirect and sandwich-type indirect ELISAs at the same sample concentration. The rSAMs we developed here may provide new insights to develop novel immunoassay-based analytical and diagnostic tools.<br />Competing Interests: Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Sebyung Kang reports financial support was provided by National Research Foundation of Korea. Sebyung Kang reports financial support was provided by Ulsan National Institute of Science and Technology.<br /> (Copyright © 2023 Elsevier B.V. All rights reserved.)
- Subjects :
- Animals
Immunoassay methods
Single-Domain Antibodies genetics
Single-Domain Antibodies chemistry
Single-Domain Antibodies immunology
Mice
Recombinant Fusion Proteins genetics
Recombinant Fusion Proteins chemistry
Antibodies immunology
Antibodies chemistry
Antibodies genetics
Rabbits
Immunoglobulin G genetics
Immunoglobulin G immunology
Enzyme-Linked Immunosorbent Assay methods
Alkaline Phosphatase genetics
Alkaline Phosphatase metabolism
Alkaline Phosphatase chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 1879-0003
- Volume :
- 251
- Database :
- MEDLINE
- Journal :
- International journal of biological macromolecules
- Publication Type :
- Academic Journal
- Accession number :
- 37573903
- Full Text :
- https://doi.org/10.1016/j.ijbiomac.2023.126299