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双功能 M13 噬菌体作为酶容器,用于增强色 - 光热双模式检测赭曲霉毒素 A。

Bifunctional M13 Phage as Enzyme Container for the Reinforced Colorimetric-Photothermal Dual-Modal Sensing of Ochratoxin A.

机构信息

State Key Laboratory of Food Science and Technology, Nanchang University, Nanchang 330047, China.

School of Food Science and Technology, Nanchang University, Nanchang 330047, China.

出版信息

Toxins (Basel). 2022 Dec 20;15(1):5. doi: 10.3390/toxins15010005.

Abstract

"Point of care" (POC) methods without expensive instruments and special technicians are greatly needed for high-throughput analysis of mycotoxins. In comparison, the most widely used screening method of the conventional enzyme-linked immunosorbent assay (ELISA) confronts low sensitivity and harmful competing antigens. Herein, we develop a plasmonic-photothermal ELISA that allows precise readout by color-temperature dual-modal signals based on enzymatic reaction-induced AuNP aggregation for highly sensitive detection of ochratoxin A (OTA). The bifunctional M13 phage carrying OTA that mimics the mimotope on the end of p3 proteins and abundant biotin molecules on the major p8 proteins is adopted as an eco-friendly competing antigen and enzyme container for amplifying the signal intensity. Under optimal conditions, both colorimetric and photothermal signals enable good dynamic linearity for quantitative OTA detection with the limits of detection at 12.1 and 8.6 pg mL, respectively. Additionally, the proposed ELISA was adapted to visual determination with a cutoff limit of 78 pg mL according to a vivid color change from deep blue to red. The recoveries of OTA-spiked corn samples indicate the high accuracy and robustness of the proposed method. In conclusion, our proposed strategy provides a promising method for eco-friendly and sensitive POC screening of OTA. Moreover, it can be easily applied to other analytes by changing the involved specific mimotope sequence.

摘要

"床边"(POC)方法不需要昂贵的仪器和特殊技术,非常适合高通量分析真菌毒素。相比之下,传统酶联免疫吸附测定(ELISA)最广泛使用的筛选方法存在灵敏度低和有害竞争抗原的问题。在此,我们开发了一种等离子体光热 ELISA,该方法基于酶反应诱导的金纳米颗粒聚集,通过颜色-温度双模态信号进行精确读出,用于高度灵敏地检测赭曲霉毒素 A(OTA)。携带 OTA 的双功能 M13 噬菌体模拟 p3 蛋白末端的模拟表位和主要 p8 蛋白上丰富的生物素分子,用作生态友好型竞争抗原和酶容器,以增强信号强度。在最佳条件下,比色和光热信号都能实现定量 OTA 检测的良好动态线性,检测限分别为 12.1 和 8.6 pg/mL。此外,根据从深蓝色到红色的明显颜色变化,提出的 ELISA 可用于可视化测定,截止值为 78 pg/mL。OTA 污染玉米样品的回收率表明该方法具有较高的准确性和稳健性。总之,我们提出的策略为 OTA 的生态友好和敏感 POC 筛选提供了一种有前途的方法。此外,通过改变所涉及的特定模拟表位序列,该方法可以很容易地应用于其他分析物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0051/9867381/ce7be6e89a97/toxins-15-00005-sch001.jpg

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