血红素
检出限
G-四倍体
脱氧核酶
生物分析
化学
适体
克莱诺碎片
生物传感器
分子生物学
聚合酶
组合化学
酶
基因
DNA
生物
生物化学
色谱法
血红素
核酸外切酶
作者
Weihua Zhao,Mingbin Liu,Hongbo Li,Suqin Wang,Shasha Tang,Rongmei Kong,Ru‐Qin Yu
标识
DOI:10.1016/j.bios.2019.111593
摘要
Accurate and sensitive detection of the Pax-5a gene is of great importance in the early diagnosis and prognosis of acute leukaemia. Herein, a label-free electrochemical sensing system was proposed for the detection of the acute leukaemia Pax-5a gene based on enzyme-assisted signal amplification to generate abundant G-quadruplex/hemin DNAzyme. The presence of Pax-5a can open the hairpin probe (HP), which acts as a template. Under the action of the restriction enzymes Nt.BbvCI and Klenow fragment polymerase, the target gene Pax-5a is cycled to open the HP; On the other hand, a large number of G-quadruplex sequences are produced. The resulting G-quadruplex sequence is capable of forming the G-quadruplex/hemin complex on the surface of the electrode in the presence of hemin. The ultrasensitive label-free electrochemical detection of Pax-5a can be realized via the G-quadruplex/hemin complex-catalysed reduction of H2O2, and the detection limit was estimated to be as low as 4.6 fM. In addition, the biosensor has good specificity and stability, and also has excellent detection capabilities in a complex substrate environment. Therefore, the sensor shows great potential in bioanalysis and clinical diagnosis.
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