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基于双酶介导的原位扩增策略的靶向激活超顺磁球形核酸纳米机器用于溶菌酶的超高灵敏 SERS 检测。

Targeted-activation superparamagnetic spherical nucleic acid nanomachine for ultrasensitive SERS detection of lysozyme based on a bienzymatic-mediated in situ amplification strategy.

机构信息

Key Laboratory of Optic-Electric Sensing and Analytical Chemistry for Life Science, Ministry of Education, Shandong Key Laboratory of Biochemical Analysis, and College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao, 266042, People's Republic of China.

Analytical and Testing Center, Qingdao University of Science and Technology, Qingdao, 266042, People's Republic of China.

出版信息

Anal Sci. 2024 Mar;40(3):429-438. doi: 10.1007/s44211-023-00471-w. Epub 2023 Dec 19.

DOI:10.1007/s44211-023-00471-w
PMID:38112960
Abstract

Lysozyme (LYS) is a widely used bacteriostatic enzyme. In this paper, we built a sensitive and accurate Raman biosensing platform to detect trace amounts of LYS. The method is based on magnetic spherical nucleic acid formed by a combination of LYS aptamer (Apt) and magnetic beads (MBs). Meanwhile, this method utilizes a dual enzyme-assisted nucleic acid amplification circuit and surface-enhanced Raman scattering (SERS). In this sensing strategy, which is based on the specific recognition of Apt, magnetic spherical nucleic acids were associated with SERS through a nucleic acid amplification circuit, and the low abundance of LYS was converted into a high-specificity Raman signal. Satellite-like MB@AuNPs were formed in the presence of the target, which separated specifically in a magnetic field, effectively avoided the interference of complex sample environment. Under the optimal sensing conditions, the concentration of LYS exhibited a good linear relationship between 1.0 × 10 and 5.0 × 10 M and the limit of detection was as low as 8.3 × 10 M. In addition, the sensor strategy shows excellent accuracy and sensitivity in complex samples, providing a new strategy for the specific detection of LYS.

摘要

溶菌酶(LYS)是一种广泛使用的抑菌酶。在本文中,我们构建了一种灵敏、准确的拉曼生物传感平台来检测痕量 LYS。该方法基于 LYS 适体(Apt)和磁性珠(MBs)结合形成的磁性球形核酸。同时,该方法利用双酶辅助核酸扩增电路和表面增强 Raman 散射(SERS)。在这种基于 Apt 特异性识别的传感策略中,磁性球形核酸通过核酸扩增电路与 SERS 相关联,将低丰度的 LYS 转化为高特异性的 Raman 信号。在存在靶标的情况下形成了类卫星状的 MB@AuNPs,它们在磁场中特异性分离,有效地避免了复杂样品环境的干扰。在最佳传感条件下,LYS 的浓度在 1.0×10 和 5.0×10 M 之间呈现良好的线性关系,检测限低至 8.3×10 M。此外,该传感器策略在复杂样品中表现出优异的准确性和灵敏度,为 LYS 的特异性检测提供了一种新策略。

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本文引用的文献

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