Issue 41, 2019, Issue in Progress

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

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 SiO2–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 via 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.

Graphical abstract: A spherical poly(acrylic acid) brush–enzyme block with high catalytic capacity for signal amplification in digital biological assays

Supplementary files

Article information

Article type
Paper
Submitted
06 May 2019
Accepted
20 Jul 2019
First published
30 Jul 2019
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2019,9, 23658-23665

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

Y. Wang, Z. Gao, J. Yi, H. Zhou, X. Fang, H. Xu, J. Zhao and H. Gu, RSC Adv., 2019, 9, 23658 DOI: 10.1039/C9RA03404H

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