Abstract
Okadaic acid (OA) is produced by Dinophysis and Prorocentrum dinoflagellates and primarily accumulates in bivalves, and this toxin has harmful effects on consumers and operators. In this work, we first report the use of aptamers as novel non-toxic probes capable of binding to a monoclonal antibody against OA (OA-mAb). Aptamers that mimic the OA toxin with high affinity and selectivity were generated by the magnetic bead-assisted systematic evolution of ligands by exponential enrichment (SELEX) strategy. After 12 selection rounds, cloning, sequencing and enzyme-linked immunosorbent assay (ELISA) analysis, four candidate aptamers (O24, O31, O39, O40) were selected that showed high affinity and specificity for OA-mAb. The affinity constants of O24, O31, O39 and O40 were 8.3 × 108 M−1, 1.47 × 109 M−1, 1.23 × 109 M−1 and 1.05 × 109 M−1, respectively. Indirect competitive ELISA was employed to determine the internal-image function of the aptamers. The results reveal that O31 has a similar competitive function as free OA toxin, whereas the other three aptamers did not bear the necessary internal-image function. Based on the derivation of the curvilinear equation for OA/O31, the equation that defined the relationship between the OA toxin content and O31 was Y = 2.185X − 1.78. The IC50 of O31 was 3.39 ng·mL−1, which was close to the value predicted by the OA ELISA (IC50 = 4.4 ng·mL−1); the IC10 was 0.33 ng·mL−1. The above data provides strong evidence that internal-image functional aptamers could be applicable as novel probes in a non-toxic assay.
Highlights
Okadaic acid (OA), a key toxin involved in diarrhoeic shellfish poisoning (DSP), and is produced by the Dinophysis and Prorocentrum dinoflagellates [1,2]
We report for the first time the development of aptamers that can mimic the OA toxin
The ic-enzyme-linked immunosorbent assay (ELISA) result revealed that only O31 had a similar function with the free OA toxin, which reacted with OA-mAb and reduced the binding probability of OA-Bovine serum albumin (BSA) and the antibody
Summary
Okadaic acid (OA), a key toxin involved in diarrhoeic shellfish poisoning (DSP), and is produced by the Dinophysis and Prorocentrum dinoflagellates [1,2]. This toxin is ingested through a filter feeding mechanism by various species of shellfish, such as bivalve mussels, scallops, oysters, and clams. This method has been prohibited since 2011 due to a lack of sensitivity, accuracy and ethical concerns For this reason, HPLC coupled to various detectors, including mass spectrometry, tandem mass spectrometry (MS/MS), and fluorescence detection are employed to quantify OA and its analogues [11,12,13,14]. OA toxicity is potentially harmful to the operator’s health
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