G-四倍体
血红素
脱氧核酶
检出限
DNA
化学
聚合酶链反应
生物物理学
细菌
适体
辣根过氧化物酶
分子生物学
生物化学
组合化学
色谱法
生物
基因
酶
遗传学
血红素
作者
Yanan Zhou,Yan Zeng,Peng Wang,Peng Qi,Yan Sun,Dun Zhang
标识
DOI:10.1016/j.snb.2023.133854
摘要
Here a colorimetric sensing platform for sulfate-reducing bacterial DNA analysis was described by using a catalytic hemin/G-quadruplex loaded rigid DNA triangle assembly. This two-dimensional rigid DNA triangle structure was assembled by target bacterial DNA and three hairpin beacon probes. As three tips of hairpin probes carry specific recognition sites for G-quadruplex formation, target bacterial DNA trigger the opening of hairpin probes, not only forming a steady rigid DNA triangle but also activating the hemin/G-quadruplex horseradish peroxidase mimicking DNAzyme. The resultant hemin/G-quadruplex loaded rigid DNA triangle assembly catalyzes a colorimetric reaction with the signal intensity correlated to target concentrations, achieving target bacterial DNA detection with a detection limit as low as 23.99 fM. We further analyzed actual bacteria with this system, by acquiring bacterial DNA including bacteria-specific sequences with polymerase chain reaction (PCR), with the detection limit down to 1 cfu/mL. The system shows good selectivity for the target and resistance to interference, highly stable performance for serum samples application, showing great potential for application in the fields of genetic analysis, environmental monitoring, and medical testing.
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