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一种用于数字生物分析中信号放大的具有高催化能力的球形聚(丙烯酸)刷酶块。

A spherical poly(acrylic acid) brush-enzyme block with high catalytic capacity for signal amplification in digital biological assays.

作者信息

Wang Yibei, Gao Zehang, Yi Jingwei, Zhou Hongbo, Fang Xiaoxia, Xu Hong, Zhao Jianlong, Gu Hongchen

机构信息

School of Biomedical Engineering, Med-X Research Institute, Shanghai Jiao Tong University Shanghai 200030 PR China

Shanghai Institute of Microsystem and Information Technology, Chinese Academy Science Shanghai 200030 PR China.

出版信息

RSC Adv. 2019 Jul 30;9(41):23658-23665. doi: 10.1039/c9ra03404h. eCollection 2019 Jul 29.

Abstract

Ultrasensitive determination of some ultra-low abundance biological molecules closely related to diseases is currently a wide concern and urgent issue to be addressed. Here, a spherical poly(acrylic acid)-alkaline phosphatase (SP-AKP) signal amplification block using spherical poly(acrylic acid) brush nanoparticles (SP) as the immobilized carriers was designed and synthesized optimally first. The results show that a single SP-AKP with high enzyme binding capacity and high catalytic ability (up to about 4800 effective free AKP per SP-AKP) has much greater fluorescence signal amplification ability than a single free AKP or SiO-COOH-AKP. Then, a droplet generation microfluidic chip was prepared successfully, and the SP-AKP was loaded and confined in a 14 pL droplet by adjusting its concentration to ensure at most one SP-AKP was encapsulated in each droplet according to Poisson's theory. Finally, the fluorescence signals produced by 4-methylumbelliferyl phosphate (4-MUP) catalyzed SP-AKP within 6 min were sufficient to be detected by a fluorescence microscope. Thus, the digital signal distribution of "1/0" (signal/background) was obtained, making this SP-AKP signal amplification block a promising enzyme label for potential high sensitivity digital biological detection applications.

摘要

超灵敏检测一些与疾病密切相关的超低丰度生物分子是当前备受关注且亟待解决的问题。在此,首先优化设计并合成了一种以球形聚丙烯酸刷状纳米颗粒(SP)作为固定载体的球形聚(丙烯酸)-碱性磷酸酶(SP-AKP)信号放大模块。结果表明,单个具有高酶结合能力和高催化能力(每个SP-AKP高达约4800个有效游离AKP)的SP-AKP比单个游离AKP或SiO-COOH-AKP具有更强的荧光信号放大能力。然后,成功制备了一种液滴生成微流控芯片,并通过调节其浓度将SP-AKP加载并限制在14 pL的液滴中,以确保根据泊松理论每个液滴中最多包封一个SP-AKP。最后,由4-甲基伞形酮磷酸酯(4-MUP)催化SP-AKP在6分钟内产生的荧光信号足以被荧光显微镜检测到。因此,获得了“1/0”(信号/背景)的数字信号分布,使得这种SP-AKP信号放大模块成为潜在高灵敏度数字生物检测应用中有前景的酶标记物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58f5/9069456/98748ce560a3/c9ra03404h-s1.jpg

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