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Updated: Jun 12, 2026

Biosensor-based High Throughput Biopanning and Bioinformatics Analysis Strategy for the Global Validation of Drug-protein Interactions
Published on: December 1, 2020
[Selecting the phage displaying tetrodotoxin mimic epitope by phage random peptide library]
Lin Zhang1, Tao Jiang, Rong Ji
1Institute of Nutrition and Food Safety, Chinese Center for Disease Control and Prevention, Beijing 100021, China.
Objective:
To screen the positive phage displaying the mimic epitope of tetrodotoxin (TTX) by using phage random peptide display library technology and to establish immunoassay for the detection of tetrodotoxin.
Methods:
Monoclonal antibody against TTX was used as a ligand to screen the binding peptide from the Ph. D.-7 peptide library. The library is displayed as a fusion protein with the coat protein III of filamentous phage M13. The positive clones were identified by ELISA. Results After four rounds of panning, 7 positive phages binding to the anti-TTX monoclone antibody were obtained, and through indirect competitive ELISA, 3 positive clones inhibiting TTX were screened. A competitive ELISA was established with phage P4, the linear range of the inhibition is 1-20 ng/ml, R2 = 0.9947, the detecting limit is 1 ng/ml.
Conclusion:
The phage display technique can be successfully applied to screen the mimic epitope of tetrodotoxin. The acquired phages may be used as the surrogate of the toxin to establish immunoassay.
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