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推进 miRNA 检测:增强型生物素-链霉亲和素双模相成像表面等离子体共振适体传感器。

Advancing MicroRNA Detection: Enhanced Biotin-Streptavidin Dual-Mode Phase Imaging Surface Plasmon Resonance Aptasensor.

机构信息

State Key Laboratory of Radio Frequency Heterogeneous Integration, Key Laboratory of Optoelectronic Devices and Systems of Ministry of Education and Guangdong Province, College of Physics and Optoelectronics Engineering, Shenzhen University, Shenzhen 518060, China.

Department of Laboratory Medicine, Shenzhen Second People's Hospital, the First Affiliated Hospital of Shenzhen University, Shenzhen 518035, China.

出版信息

Anal Chem. 2024 May 28;96(21):8791-8799. doi: 10.1021/acs.analchem.4c01234. Epub 2024 May 14.

Abstract

MicroRNAs (miRNAs) are novel tumor biomarkers owing to their important physiological functions in cell communication and the progression of multiple diseases. Due to the small molecular weight, short sequence length, and low concentration levels of miRNA, miRNA detection presents substantial challenges, requiring the advancement of more refined and sensitive techniques. There is an urgent demand for the development of a rapid, user-friendly, and sensitive miRNA analysis method. Here, we developed an enhanced biotin-streptavidin dual-mode phase imaging surface plasmon resonance (PI-SPR) aptasensor for sensitive and rapid detection of miRNA. Initially, we evaluated the linear sensing range for miRNA detection across two distinct sensing modalities and investigated the physical factors that influence the sensing signal in the aptamer-miRNA interaction within the PI-SPR aptasensor. Then, an enhanced biotin-streptavidin amplification strategy was introduced in the PI-SPR aptasensor, which effectively reduced the nonspecific adsorption by 20% and improved the limit of detection by 548 times. Furthermore, we have produced three types of tumor marker chips, which utilize the rapid sensing mode (less than 2 min) of PI-SPR aptasensor to achieve simultaneous detection of multiple miRNA markers in the serum from clinical cancer patients. This work not only developed a new approach to detect miRNA in different application scenarios but also provided a new reference for the application of the biotin-streptavidin amplification system in the detection of other small biomolecules.

摘要

微小 RNA(miRNA)是新型肿瘤生物标志物,因为它们在细胞通讯和多种疾病的进展中具有重要的生理功能。由于 miRNA 分子量小、序列短、浓度低,因此 miRNA 的检测具有很大的挑战性,需要更精细和灵敏的技术。人们迫切需要开发一种快速、易用和灵敏的 miRNA 分析方法。在这里,我们开发了一种增强型的生物素-链霉亲和素双模式相衬表面等离子体共振(PI-SPR)适体传感器,用于灵敏和快速检测 miRNA。首先,我们评估了两种不同传感模式下 miRNA 检测的线性传感范围,并研究了在 PI-SPR 适体传感器中适体-miRNA 相互作用中影响传感信号的物理因素。然后,我们在 PI-SPR 适体传感器中引入了增强型生物素-链霉亲和素放大策略,该策略有效减少了 20%的非特异性吸附,并将检测限提高了 548 倍。此外,我们还制作了三种肿瘤标志物芯片,利用 PI-SPR 适体传感器的快速传感模式(不到 2 分钟),实现了对临床癌症患者血清中多种 miRNA 标志物的同时检测。这项工作不仅开发了一种在不同应用场景下检测 miRNA 的新方法,还为生物素-链霉亲和素放大系统在检测其他小分子生物标志物中的应用提供了新的参考。

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