生物传感器
脱氧核酶
清脆的
检出限
适体
类鼻疽伯克霍尔德菌
化学
组合化学
DNA
纳米技术
计算生物学
材料科学
细菌
分子生物学
生物
生物化学
色谱法
基因
遗传学
作者
Cai Li,Changjin Liu,Rui Liu,Yuexin Wang,Anyang Li,Shen Tian,Wei Cheng,Shijia Ding,Wenting Li,Min Zhao,Qianfeng Xia
标识
DOI:10.1016/j.bios.2023.115098
摘要
In this work, PtPd nanoparticles functionalized porphyrin metal-organic framework nanoenzymes (PtPd@PCN-224 nanoenzymes) are exploited as signal amplification tags to fabricate a rapid and ultrasensitive sensitive CRISPR/Cas14a-based electrochemical biosensor for Burkholderia pseudomallei (B. pseudomallei) specific DNA sequences detection. The prepared PtPd@PCN-224 nanoenzymes not only catalyze the reduction peak current of H2O2 to obtain a strong electrochemical signal output, but also provide massive active sites for the assembly of nucleic acids by Zr-O-P bonds. Besides, the designed target-activated CRISPR/Cas14a is able to recognize the target DNA sequences and further trigger the trans-cleavage of ssDNA for signal amplification. Benefiting from the target-activated CRISPR/Cas14a and PtPd@PCN-224 nanoenzymes, the developed electrochemical biosensor for B. pseudomallei DNA detection exhibits high sensitivity with detection of limit down to 12.8 aM and excellent specificity for distinguishing non-targeted bacteria. Moreover, the CRISPR/Cas14a-based electrochemical detection platform can also apply for other pathogenic bacteria diagnostic by well-designing sgRNA for target sequence recognition, possessing high flexibility and versatility in clinical diagnosis.
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