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三螺旋分子开关驱动的滚环扩增和催化发夹组装多级信号放大荧光适体传感器用于检测黄曲霉毒素 B1。

Triple-helix molecular-switch-actuated rolling circle amplification and catalytic hairpin assembly multistage signal amplified fluorescent aptasensor for detection of aflatoxin B1.

机构信息

College of Food Science and Technology, Henan Key Laboratory of Cereal and Oil Food Safety Inspection and Control, Henan University of Technology, Zhengzhou, 450001, China.

College of Food Science and Technology, Henan Key Laboratory of Cereal and Oil Food Safety Inspection and Control, Henan University of Technology, Zhengzhou, 450001, China.

出版信息

Anal Chim Acta. 2024 Sep 22;1323:343072. doi: 10.1016/j.aca.2024.343072. Epub 2024 Aug 6.

Abstract

BACKGROUND

Mycotoxins, a class of secondary metabolites produced by molds, are widely distributed in nature and are very common in food contamination. Aflatoxin B1 (AFB1) is a highly stable natural mycotoxin, and many agricultural products are easily contaminated by AFB1, it is important to establish a sensitive and efficient AFB1 detection method for food safety. The fluorescence aptamer sensor has shown satisfactory performance in AFB1 detection, but most of the fluorescence aptasensors are not sensitive enough, so improving the sensitivity of the aptasensor becomes the focus of this work.

RESULTS

Herein, an innovative fluorescent aptasensor for AFB1 detection which is based on catalytic hairpin assembly (CHA) and rolling circle amplification (RCA) driven by triple helix molecular switch (THMS) is proposed. A functional single-strand with an AFB1 aptamer, here called an APF, is first designed to lock onto the signal transduction probe (STP), which separates from THMS when target AFB1 is present. Subsequently, STP initiates the RCA reaction along the circular probe, syntheses macro-molecular mass products through repeated triggering sequences, triggers the CHA reaction to produce a large number of H1-H2 structures, which causes FAM to move away from BHQ-1 and recover its fluorescence signal. The fluorescence signal from FAM at 520 nm was collected as the signal output of aptasensor in this work. With high amplification efficiency of RCA and CHA of the fluorescence sensor, resulting in a low LOD value of 2.95 pg mL(S/N = 3).

SIGNIFICANCE

The successful establishment of the sensor designed in this work shows that the cascade amplification reaction is perfectly applied in the fluorescent aptamer sensor, and the signal amplification through the reaction between DNA strands is a simple and efficient method. In addition, it's also important to remember that the aptasensor can detect other targets only by changing the sequence of the aptamer, without redesigning other DNA sequences in the reaction system.

摘要

背景

真菌产生的次生代谢产物霉菌毒素广泛存在于自然界中,且在食品污染中非常常见。黄曲霉毒素 B1(AFB1)是一种非常稳定的天然霉菌毒素,许多农产品容易受到 AFB1 的污染,因此建立一种用于食品安全的灵敏高效的 AFB1 检测方法非常重要。荧光适体传感器在 AFB1 检测中表现出了令人满意的性能,但大多数荧光适体传感器的灵敏度不够高,因此提高适体传感器的灵敏度成为了这项工作的重点。

结果

在此,提出了一种基于三螺旋分子开关(THMS)驱动的催化发夹组装(CHA)和滚环扩增(RCA)的新型 AFB1 荧光适体传感器。首先设计了一条带有 AFB1 适体的功能性单链,称为 APF,当存在目标 AFB1 时,它与信号转导探针(STP)锁定,而 STP 从 THMS 上分离。随后,STP 沿着环形探针启动 RCA 反应,通过重复触发序列合成大分子质量产物,触发 CHA 反应产生大量 H1-H2 结构,从而使 FAM 远离 BHQ-1 并恢复其荧光信号。本工作中,将 FAM 在 520nm 处的荧光信号作为适体传感器的信号输出。由于 RCA 和 CHA 的高放大效率,使得该荧光传感器的检测限(LOD)值低至 2.95pgmL(S/N=3)。

意义

本工作设计的传感器的成功建立表明级联放大反应在荧光适体传感器中得到了完美的应用,并且通过 DNA 链之间的反应进行信号放大是一种简单高效的方法。此外,还需要记住的是,通过改变适体的序列,适体传感器可以检测其他目标,而无需重新设计反应系统中的其他 DNA 序列。

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