Ultrasensitive and rapid colorimetric detection of paraquat via a high specific VHH nanobody

百草枯 化学 淘选 免疫原 检出限 免疫分析 分析灵敏度 色谱法 分子生物学 抗体 单克隆抗体 肽库 生物化学 生物 肽序列 免疫学 基因 医学 替代医学 病理
作者
Qian Zhang,Lihua Li,Yu Wang,Hong Wang,Zhenlin Xu,Yuanxin Tian,Yuanming Sun,Jinyi Yang,Yu‐Dong Shen
出处
期刊:Biosensors and Bioelectronics [Elsevier]
卷期号:205: 114089-114089 被引量:27
标识
DOI:10.1016/j.bios.2022.114089
摘要

Rapid and quantitative detection of paraquat is crucial because of its high toxicity. Here, we developed an ultrasensitive time-resolved fluorescence immunochromatographic assay (TRFICA) strip based on our synthesized variable domain of heavy chain antibody (VHH, also called Nanobody) for paraquat detection. Briefly, the specific immunogen selected from six designed antigens was employed to immunize alpaca, and a high-efficiency capacity of 1.6 × 1013 pfu mL-1 phage display nanobody library was established for biopanning against paraquat. The selected nanobody exhibited high sensitivity (limit of detection (LOD) was 0.0090 ng mL-1 and IC50 was 0.0588 ng mL-1 in buffer) and stability to high temperatures and denaturants. The molecular docking results indicated that the π-π, cation-π, and hydrogen bond interactions between paraquat and the pocket-like structures of complementarity-determining regions (CDRs) in VHH played a critical role in the antibody-paraquat recognition, competition, and affinity processes. The constructed TRFICA recognized paraquat through a quantitative analysis using the strip reader, and showed no cross-reactivity with other herbicides, and a semi-quantitative analysis using the naked eye. Notably, the potential practical applications of the TRFICA evaluated by performing a quantitative analysis of paraquat in food samples (vegetables, fruits, and grain products) and biological samples (blood and urine) showed a recovery rate range between 76.7% and 133.3% with inter-assay coefficient variation lower than 18.5%. The nanobody from phage display libraries was effective for small molecule recognition and detection, and it is a vital tool for immunoassay.
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