核酸
底漆(化妆品)
病菌
化学
聚合酶链反应
多重位移放大
分子信标
病毒学
检出限
DNA
分子生物学
生物化学
色谱法
微生物学
DNA提取
生物
寡核苷酸
有机化学
基因
作者
Ye Zhang,Zihua Li,Wanting Su,Guangzhi Zhong,Xiaohe Zhang,Yuan Wu,Bo Situ,Yunju Xiao,Xiaohui Yan,Lei Zheng
标识
DOI:10.1016/j.aca.2022.340125
摘要
Existing detection methods for pathogen nucleic acid detection, such as polymerase chain reaction (PCR), are complicated and expensive to perform. Here, we report a simple and versatile strategy for highly sensitive detection of pathogen nucleic acid based on toehold-mediated strand displacement initiated primer exchange amplification (t-PER). In the presence of the target, the blocked hairpin substrate is released by toehold-mediated strand displacement, which triggers the primer exchange reaction amplification. Then, multiple long tandem-repeat single-strands generated by PER open the molecular beacon to recover the fluorescence signal. The t-PER protocol also successfully directly detected human papilloma virus from clinical cervical swab samples, with consistent results compared to real time-polymerase chain reaction (RT-PCR). Moreover, the versatility and clinical feasibility of this method was further confirmed by measuring Epstein-Barr virus, hepatitis B virus, and Ureaplasma urealyticum from different clinical samples (serum samples and urine samples). This simple platform enabled specific and sensitive detection of pathogen nucleic acid in a format that might hold great potential for point-of-care infection diagnosis.
科研通智能强力驱动
Strongly Powered by AbleSci AI