Bactrian camel nanobody-based immunoassay for specific and sensitive detection of Cry1Fa toxin
The variable domain of the heavy-chain-only antibody (VHH) or nanobody (Nb), derived from camelids, begins to play an important role on the detection of protein markers. In this study, we constructed a phage-displayed library of VHHs against Cry1Fa by immunizing a healthy Bactrian camel with Cry1Fa...
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Veröffentlicht in: | Toxicon (Oxford) 2014-12, Vol.92, p.186-192 |
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Sprache: | eng |
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Zusammenfassung: | The variable domain of the heavy-chain-only antibody (VHH) or nanobody (Nb), derived from camelids, begins to play an important role on the detection of protein markers. In this study, we constructed a phage-displayed library of VHHs against Cry1Fa by immunizing a healthy Bactrian camel with Cry1Fa toxin. After a series of bio-panning and screening by phage display technology, three anti-Cry1Fa nanobodies (Nbs) with great difference in complementarity determining region 3 (CDR3) were obtained and they were highly specific to Cry1Fa as well as showed full of activity when exposed to 70 °C for 3 h. Through modifying Nbs with Horseradish Peroxidase (HRP) and biotin, two Nbs which can recognize the different epitopes of Cry1Fa were determined and they were used to establish a novel sandwich immune ELISA based on biotin-SA interaction for Cry1Fa detection. The immunoassay exhibited a linear range from 1 to 100 ng/mL with a detection limit of 0.88 ng/mL. The recoveries from spiked corn and soybean samples were ranged from 83.33 to 117.17%, with a coefficient of variation (C.V) less than 6.0%. All together, the proposed immunoassay will be a promising way for sensitive and accurate determination of Cry1Fa toxin.
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•A novel sandwich immunoassay based on nanobody for Cry1Fa detection.•An immune library of nanobody against Cry1Fa toxin was generated.•The immunoassay exhibited a working range of 1–100 ng/mL for Cry1Fa.•The sandwich immune system exhibited acceptable sensitivity and reproducibility. |
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ISSN: | 0041-0101 1879-3150 |
DOI: | 10.1016/j.toxicon.2014.10.024 |