Fabrication of Fragment Antibody-Enzyme Complex as a Sensing Element for Immunosensing.

Int J Mol Sci

Department of Biotechnology and Life Science, Graduate School of Engineering, Tokyo University of Agriculture and Technology, Tokyo 184-8588, Japan.

Published: January 2022

AI Article Synopsis

  • Antibody-enzyme complexes (AECs) are powerful tools for immunosensing because they combine target binding and signal generation through catalytic activity, especially from oxidoreductases.
  • The use of fragment antibodies instead of intact ones, like immunoglobulin G (IgG), helps address ethical concerns and reduce production costs.
  • Various fabrication methods for AECs, including direct fusion, enzymatic conjugation, and Catcher/Tag systems, are reviewed, highlighting their pros and cons for creating effective sensing applications.

Article Abstract

Antibody-enzyme complexes (AECs) are ideal molecular recognition elements for immunosensing applications. One molecule possesses both a binding ability to specific targets and catalytic activity to gain signals, particularly oxidoreductases, which can be integrated into rapid and sensitive electrochemical measurements. The development of AECs using fragment antibodies rather than intact antibodies, such as immunoglobulin G (IgG), has attracted attention for overcoming the ethical and cost issues associated with the production of intact antibodies. Conventionally, chemical conjugation has been used to fabricate AECs; however, controlling stoichiometric conjugation using this method is difficult. To prepare homogeneous AECs, methods based on direct fusion and enzymatic conjugation have been developed, and more convenient methods using Catcher/Tag systems as coupling modules have been reported. In this review, we summarize the methods for fabricating AECs using fragment antibodies developed for sensing applications and discuss the advantages and disadvantages of each method.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8836092PMC
http://dx.doi.org/10.3390/ijms23031335DOI Listing

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