College of Pharmacy, Weifang Medical University, Weifang 261053, China.
Analyst. 2019 Dec 16;145(1):46-51. doi: 10.1039/c9an01853k.
Development of a simple, fast, cost-efficient and sensitive approach for accurate protein analysis is of high significance due to its potential application in disease diagnosis and biomedicine research. Thus, we established a label-free fluorescence DNA walker for streptavidin detection based on terminal protection and dual enzyme assisted cleavage induced G-quadruplex/berberine conformation. In this paper, the swing arm probe and report probe were pre-assembled on gold nanoparticles. With the addition of a target, through the high-efficiency affinity between streptavidin and biotin in order to prevent the hydrolysis of exonuclease I, the swing arm probe which contains 8-17 DNAzyme cannot be destroyed and plays a role in the catalytic cleavage of the report probe, and the liberating fragment of the report probe which contains a specific sequence (5'-(TTAGGG)4) of G-quadruplex units can combine with berberine and shows an evident fluorescence signal enhancement. Our method, a sensitive and selective method of protein detection, achieves a 20 pM detection limit toward streptavidin. This developed DNA walker, which combines terminal protection and a dual enzyme assisted strategy, provides a prospective channel for streptavidin detection and should also be used for the design of biosensors in bio-detection and disease diagnosis.
由于其在疾病诊断和生物医学研究中的潜在应用,开发一种简单、快速、经济高效且灵敏的方法来准确分析蛋白质具有重要意义。因此,我们建立了一种基于末端保护和双酶辅助切割诱导的 G-四联体/小檗碱构象的无标记荧光 DNA walker 来检测链霉亲和素。在本文中,摆动臂探针和报告探针预先组装在金纳米粒子上。随着目标的加入,通过链霉亲和素和生物素之间的高效亲和力,以防止外切酶 I 的水解,包含 8-17 个 DNA 酶的摆动臂探针不能被破坏,并在报告探针的催化切割中发挥作用,报告探针的释放片段包含 G-四联体单元的特定序列(5'-(TTAGGG)4)可以与小檗碱结合并显示出明显的荧光信号增强。我们的方法是一种灵敏且选择性的蛋白质检测方法,对链霉亲和素的检测限达到 20 pM。这种结合末端保护和双酶辅助策略的 DNA walker 为链霉亲和素的检测提供了一个有前景的途径,也应该用于生物检测和疾病诊断中生物传感器的设计。