Gong Xiaoyu, Yu Chi, Zhang Yichang, Sun Yuan, Ye Lin, Li Juan
Longgang District People's Hospital of Shenzhen Shenzhen Guangdong 518172 P. R. China.
Hubei Key Laboratory of Resources and Chemistry of Chinese Medicine, Hubei University of Chinese Medicine Wuhan Hubei 430065 P. R. China
RSC Adv. 2019 Oct 22;9(58):33898-33902. doi: 10.1039/c9ra06798a. eCollection 2019 Oct 18.
A carbon nanoparticle (CNP) and Cryonase-aided method that realizes the amplified fluorescent detection of theophylline was proposed. The amplification technique exploits distinct binding affinities of CNP towards the FAM-labeled theophylline RNA aptamer (aptasensor) and aptasensor/theophylline complex as well as the protection effect of CNP for absorbed aptasensor from enzymatic digestion by Cryonase. Upon the addition of theophylline, it forms an aptasensor/theophylline complex with a fluorescent dye-tagged aptasensor that is initially absorbed and quenched by CNP. The nuclease activity of Cryonase towards detached aptasensor probes is then activated, leading to efficient cleavage of aptasensor probes and separation of the fluorescent dye from the CNP surface. Theophylline that has been liberated can launch another reaction cycle, which ensures the sensitivity enhancement. A detection limit is achieved as high as 6.3 nM, which is 400-fold better than traditional strategies. The proposed sensing system also provides desired selectivity even in serum samples. The assay is simple, sensitive, selective, and universal, and has great promise for the design and application of aptasensors in the biological, chemical, and biomedical fields.
提出了一种实现茶碱荧光放大检测的碳纳米颗粒(CNP)与低温酶辅助方法。该放大技术利用了CNP对FAM标记的茶碱RNA适体(适体传感器)和适体传感器/茶碱复合物的不同结合亲和力,以及CNP对吸附的适体传感器免受低温酶酶解的保护作用。加入茶碱后,它与最初被CNP吸附并淬灭的荧光染料标记的适体传感器形成适体传感器/茶碱复合物。然后激活低温酶对分离的适体传感器探针的核酸酶活性,导致适体传感器探针的有效切割以及荧光染料从CNP表面分离。释放出的茶碱可以启动另一个反应循环,这确保了灵敏度的提高。实现了低至6.3 nM的检测限,比传统策略好400倍。所提出的传感系统即使在血清样本中也具有所需的选择性。该检测方法简单、灵敏、选择性好且具有通用性,在生物、化学和生物医学领域的适体传感器设计和应用方面具有巨大潜力。