Chen Chun, Li Baoxin
Key Laboratory of Analytical Chemistry for Life Science of Shaanxi Province, School of Chemistry & Chemical Engineering, Shaanxi Normal University, Xi'an 710062, China.
J Mater Chem B. 2013 May 21;1(19):2476-2481. doi: 10.1039/c3tb20270d. Epub 2013 Apr 16.
We report an amplified chemiluminescence (CL) biosensing platform for ultrasensitive DNA detection. It is based on exonuclease III-assisted target recycling amplification and the super quenching efficiency of graphene oxide (GO). In the presence of target DNA, the target-probe hybrid forms a double-stranded structure, and exonuclease III catalyzes the stepwise removal of mononucleotides from the fluorescein-labeled probe DNA, resulting in the recycling of the target DNA and CL signal amplification of the luminol-HO-HRP-fluorescein chemiluminescence resonance energy transfer (CRET) system. The detection limit of target DNA was estimated to be as low as 9 fM, and the sensitivity was about 3 orders of magnitude better than that of GO-based fluorescence resonance energy transfer (FRET) sensors for DNA with exonuclease III-assisted amplification. This CL biosensor offers the advantages of being facile, sensitive, rapid and cost-effective.
我们报道了一种用于超灵敏DNA检测的增强化学发光(CL)生物传感平台。它基于核酸外切酶III辅助的靶标循环扩增以及氧化石墨烯(GO)的超强猝灭效率。在存在靶标DNA的情况下,靶标-探针杂交体形成双链结构,核酸外切酶III催化从荧光素标记的探针DNA逐步去除单核苷酸,导致靶标DNA的循环以及鲁米诺-H₂O₂-辣根过氧化物酶-荧光素化学发光共振能量转移(CRET)系统的CL信号放大。靶标DNA的检测限估计低至9 fM,灵敏度比基于GO的具有核酸外切酶III辅助扩增的DNA荧光共振能量转移(FRET)传感器高出约3个数量级。这种CL生物传感器具有简便、灵敏、快速且经济高效的优点。