Gao Yuanyuan, Yu Hong, Tian Jingjing, Xiao Botao
Guangdong Provincial Key Laboratory of Fermentation and Enzyme Engineering, School of Biology and Biological Engineering, South China University of Technology, Guangzhou 510006, China.
State Key Laboratory of Marine Resource Utilization in South China Sea, School of Material Science and Engineering, Hainan University, Haikou 570228, China.
Nanomaterials (Basel). 2021 Oct 3;11(10):2608. doi: 10.3390/nano11102608.
Based on a fluorescence "on-off-on" strategy, we fabricated a simple and highly sensitive DNA-based fluorescence biosensor for the detection of micro (mi)RNA from carbon dots (CDs) and graphene oxide (GO) without complicated and time-consuming operations. CDs were successfully synthesized and conjugated to the end of a single-stranded fuel DNA that was adsorbed onto the surface of GO through π-π stacking, resulting in fluorescence quenching. In the presence of the target miRNA let-7a, the fuel DNA was desorbed from the GO surface, and fluorescence was restored through two successive toehold-mediated strand displacement reactions on double-stranded DNA-modified gold nanoparticles. The target miRNA let-7a was recycled, leading to signal amplification. The concentration of let-7a was proportional to the degree of fluorescence recovery. Under optimal conditions, there was a good linear relationship between the relative fluorescence intensity and let-7a concentration in the range of 0.01-1 nM, with a detection limit of 7.8 pM. With its advantages of signal amplification and high biocompatibility, this fluorescence sensing strategy can be applied to the detection of a variety of target miRNAs and can guide the design of novel biosensors with improved properties.
基于荧光“开-关-开”策略,我们制备了一种简单且高灵敏度的基于DNA的荧光生物传感器,用于从碳点(CDs)和氧化石墨烯(GO)检测微小RNA(miRNA),无需复杂且耗时的操作。成功合成了碳点,并将其与通过π-π堆积吸附在氧化石墨烯表面的单链燃料DNA末端共轭,导致荧光猝灭。在目标miRNA let-7a存在的情况下,燃料DNA从氧化石墨烯表面解吸,并通过在双链DNA修饰的金纳米颗粒上连续两次由链置换介导的反应恢复荧光。目标miRNA let-7a被循环利用,导致信号放大。let-7a的浓度与荧光恢复程度成正比。在最佳条件下,相对荧光强度与let-7a浓度在0.01 - 1 nM范围内具有良好的线性关系,检测限为7.8 pM。凭借其信号放大和高生物相容性的优点,这种荧光传感策略可应用于多种目标miRNA的检测,并可指导设计具有改进性能的新型生物传感器。