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Development of tetravalent antibody–enzyme complexes employing a lactate oxidase and the application to electrochemical immunosensors

Oda, Miho LU ; Hiraka, Kentaro ; Tsugawa, Wakako ; Ikebukuro, Kazunori ; Sode, Koji and Asano, Ryutaro (2025) In Biosensors and Bioelectronics 267.
Abstract

Antibody–enzyme complexes (AECs) are ideal for immunosensing. Although AECs using antibody fragments can be produced by bacterial hosts, their low affinity limits their sensing applications. We have improved the affinity of AECs by combining two antibodies using Catcher/Tag systems; however, it requires multiple antibodies and an enzyme production process. In this study, to realize the production of AECs harboring multiple antibody fragments in a single production process, we report a versatile development method of unique AECs based on a multimeric enzyme structure. Using the homotetrameric enzyme, lactate oxidase (LOx), as a labeling enzyme, tetravalent AECs were developed as an electrochemical immunosensor. Homogeneous tetravalent... (More)

Antibody–enzyme complexes (AECs) are ideal for immunosensing. Although AECs using antibody fragments can be produced by bacterial hosts, their low affinity limits their sensing applications. We have improved the affinity of AECs by combining two antibodies using Catcher/Tag systems; however, it requires multiple antibodies and an enzyme production process. In this study, to realize the production of AECs harboring multiple antibody fragments in a single production process, we report a versatile development method of unique AECs based on a multimeric enzyme structure. Using the homotetrameric enzyme, lactate oxidase (LOx), as a labeling enzyme, tetravalent AECs were developed as an electrochemical immunosensor. Homogeneous tetravalent AECs were successfully fabricated by fusing the anti-epidermal growth factor receptor (EGFR) variable domain of a heavy chain of heavy chain antibody to the N-terminus of LOx. The prepared AECs bound to EGFR, maintain their enzyme activity, and worked well as sensing elements in electrochemical sandwich enzyme-linked immunosorbent assay. Moreover, tetravalent AECs exhibited higher sensitivity than monovalent AECs because of their avidity. The fabricated AECs were successfully used in a wash-free homogeneous electrochemical detection system combined with magnetic separation. Our findings offer new insights into the applications of the LOx tetrameric enzyme for the fabrication of AECs with tetravalent antibodies, which may serve as scaffolds for immunosensors.

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author
; ; ; ; and
publishing date
type
Contribution to journal
publication status
published
keywords
Antibody–enzyme complex, Epidermal growth factor receptor, Homogeneous electrochemical detection, Labeling enzyme, Lactate oxidase, Variable domain of heavy chain of heavy chain antibody
in
Biosensors and Bioelectronics
volume
267
article number
116741
publisher
Elsevier
external identifiers
  • pmid:39250870
  • scopus:85203249375
ISSN
0956-5663
DOI
10.1016/j.bios.2024.116741
language
English
LU publication?
no
additional info
Publisher Copyright: © 2024 The Authors
id
60722e83-5865-4877-b39e-e2395928f792
date added to LUP
2025-08-21 15:13:08
date last changed
2025-10-16 21:08:53
@article{60722e83-5865-4877-b39e-e2395928f792,
  abstract     = {{<p>Antibody–enzyme complexes (AECs) are ideal for immunosensing. Although AECs using antibody fragments can be produced by bacterial hosts, their low affinity limits their sensing applications. We have improved the affinity of AECs by combining two antibodies using Catcher/Tag systems; however, it requires multiple antibodies and an enzyme production process. In this study, to realize the production of AECs harboring multiple antibody fragments in a single production process, we report a versatile development method of unique AECs based on a multimeric enzyme structure. Using the homotetrameric enzyme, lactate oxidase (LOx), as a labeling enzyme, tetravalent AECs were developed as an electrochemical immunosensor. Homogeneous tetravalent AECs were successfully fabricated by fusing the anti-epidermal growth factor receptor (EGFR) variable domain of a heavy chain of heavy chain antibody to the N-terminus of LOx. The prepared AECs bound to EGFR, maintain their enzyme activity, and worked well as sensing elements in electrochemical sandwich enzyme-linked immunosorbent assay. Moreover, tetravalent AECs exhibited higher sensitivity than monovalent AECs because of their avidity. The fabricated AECs were successfully used in a wash-free homogeneous electrochemical detection system combined with magnetic separation. Our findings offer new insights into the applications of the LOx tetrameric enzyme for the fabrication of AECs with tetravalent antibodies, which may serve as scaffolds for immunosensors.</p>}},
  author       = {{Oda, Miho and Hiraka, Kentaro and Tsugawa, Wakako and Ikebukuro, Kazunori and Sode, Koji and Asano, Ryutaro}},
  issn         = {{0956-5663}},
  keywords     = {{Antibody–enzyme complex; Epidermal growth factor receptor; Homogeneous electrochemical detection; Labeling enzyme; Lactate oxidase; Variable domain of heavy chain of heavy chain antibody}},
  language     = {{eng}},
  month        = {{01}},
  publisher    = {{Elsevier}},
  series       = {{Biosensors and Bioelectronics}},
  title        = {{Development of tetravalent antibody–enzyme complexes employing a lactate oxidase and the application to electrochemical immunosensors}},
  url          = {{http://dx.doi.org/10.1016/j.bios.2024.116741}},
  doi          = {{10.1016/j.bios.2024.116741}},
  volume       = {{267}},
  year         = {{2025}},
}