Recombinant aequorin with a reactive cysteine residue for conjugation with maleimide-activated antibody
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Updated: Jul 5, 2026

Synthesis of Protein Bioconjugates via Cysteine-maleimide Chemistry
Published on: July 20, 2016
Satoshi Inouye1, Jun-ichi Sato
1Yokohama Research Center, Chisso Corporation, Kanazawa-ku, Yokohama 236-8605, Japan. sinouye@chisso.co.jp
Abstract:
The mutated recombinant aequorin with a reactive cysteine residue (Cys-aequorin) was highly purified and then conjugated with a maleimide-activated antibody without significant loss of luminescence activity. The conjugate ratio of Cys-aequorin to heavy chain of immunoglobulin G (IgG) was estimated to be 1:1. To test the bioluminescent immunoassay with aequorin-labeled antibody, alpha-fetoprotein (AFP), a serological marker of liver cancer, was used as a model analyte. The measurable range of AFP was 0.02 to 200 ng/ml with the coefficient of variation between 2.1 and 4.5%.

