G-四倍体
脱氧核酶
化学
生物传感器
化学发光
组合化学
共价键
检出限
血红素
纳米技术
DNA
酶
血红素
生物化学
色谱法
有机化学
材料科学
作者
Yun Chen,Dehui Qiu,Xiaobo Zhang,Yuan Liu,Ming Cheng,Jianping Lei,Jean‐Louis Mergny,Huangxian Ju,Jun Zhou
标识
DOI:10.1021/acs.analchem.1c04842
摘要
G-quadruplex/hemin (G4/hemin) DNAzymes are biosensing systems, but their application remains limited by an overall low activity and a rather high level of unwarranted background reactions. Here, these issues were addressed through the rational design of F3T-azaC-hemin, a G4-based construct in which the hemin is covalently linked to the G4 core and its binding site flanked with a nucleotide activator, here d(T-azaC). This design led to a G4-DNAzyme whose performances have been ca. 150-fold increased compared to the parent G4-based system. The utility of F3T-azaC-hemin was demonstrated here through the ultrasensitive chemiluminescent detection of miRNA-221. The limit of detection (LOD) has been decreased to the femtomolar range, making it a new and highly efficient molecular tool in the biosensing technology field.
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