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基于适体的敏感荧光β-乳球蛋白食物过敏原生物测定法,通过双重和循环双向链置换扩增。

Aptamer-based sensitive fluorescence β-lactoglobulin food allergen bioassay via dual and cyclic bidirectional strand displacement amplifications.

机构信息

Key Laboratory of Luminescence Analysis and Molecular Sensing, Ministry of Education, School of Chemistry and Chemical Engineering, Southwest University, Chongqing, 400715, People's Republic of China.

School of Chemistry and Chemical Engineering, Chongqing University of Technology, Chongqing, 400054, People's Republic of China.

出版信息

Anal Bioanal Chem. 2024 Dec;416(29):7141-7149. doi: 10.1007/s00216-024-05618-w. Epub 2024 Nov 1.

Abstract

β-Lactoglobulin (β-Lg) is a prevalent allergenic protein found in most dairy products, which poses great food safety risks for individuals with allergies, especially for infants. Sensitive and effective detection methods for such allergens are essential to reduce the risk of allergies in daily life. Herein, a fluorescent aptamer bioassay based on a dual and cyclic bidirectional strand displacement means is developed for the sensitive detection of β-Lg in infant rice porridge and milk. The aptamer in the duplex DNA probe binds β-Lg to release the assistance strand to further hybridize with two hairpins, which triggers the initiation of two cyclic amplification cycles through the polymerization, displacement, and nicking of the strands under the action of DNA polymerase and endonuclease restriction enzymes. The amplification cycles lead to the unfolding of many fluorescently quenched signal probes to exhibit substantially enhanced fluorescence recovery for detecting β-Lg. The assay can realize detection of β-Lg in concentrations as low as 4.41 pM within the range of 0.01 to 10 nM. Furthermore, our sensing method has the capability to discriminate β-Lg from other proteins with high selectivity, resulting in low levels of β-Lg detection in rice porridge and milk samples, demonstrating promising potentials of the developed sensing method for monitoring various food allergens.

摘要

β-乳球蛋白(β-Lg)是一种普遍存在的过敏原蛋白,存在于大多数乳制品中,对过敏人群,尤其是婴儿,构成了巨大的食品安全风险。因此,需要开发敏感且有效的检测方法来降低日常生活中过敏的风险。在此,我们开发了一种基于双链和循环双向链置换的荧光适体生物测定法,用于检测婴儿米粥和牛奶中的β-Lg。双螺旋 DNA 探针中的适体与β-Lg 结合,释放出辅助链,进一步与两个发夹杂交,在 DNA 聚合酶和内切酶限制酶的作用下,引发聚合、置换和链切割的两个循环扩增。扩增循环导致许多荧光猝灭信号探针展开,从而表现出显著增强的荧光恢复,用于检测 β-Lg。该测定法可以在 0.01 到 10 nM 的范围内检测到低至 4.41 pM 的 β-Lg。此外,我们的传感方法具有从其他蛋白质中高选择性地区分 β-Lg 的能力,从而可以在米粥和牛奶样品中检测到低水平的 β-Lg,这表明所开发的传感方法在监测各种食物过敏原方面具有广阔的应用前景。

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