端粒酶
端粒
清脆的
赫拉
化学
反式激活crRNA
DNA
劈理(地质)
核糖核酸
计算生物学
分子生物学
Cas9
生物
细胞
基因
生物化学
古生物学
断裂(地质)
作者
Peihang Yu,Tiantian Yang,Decai Zhang,Lulu Xu,Xiaoxue Cheng,Shijia Ding,Wei Cheng
标识
DOI:10.1016/j.aca.2021.338404
摘要
As one of the crucial factors associated with human life span and cancer progression, telomerase is regarded as an emerging biomarker for cancer diagnosis. Therefore, a facile, rapid and sensitive approach for telomerase activity detection with point-of-care (POC) diagnosis potential is in great demands. Herein, an all-in-one telomerase activity detection assay was established based on the telomere synthesis activated CRISPR-Cas12a system. A telomerase extension reaction generated telomere repeats sequences (TTAGGG)n, which was recognized by a customized CRISPR-guided RNA (crRNA) simultaneously, and finally activated a typical trans-cleavage based CRISPR-Cas12a detection assay. With the inherent sensitivity of CRISPR-Cas12a, this approach achieved a great linear regression ranging from 100 to 2000 HeLa cells and a limitation of detection down to 26 HeLa cells. Moreover, by using the proposed method, telomerase can be detected in one pot under isothermal condition (37 °C) by a simple and fast workflow (one step within 1 h). Due to its excellent performance, this all-in-one method shows great potential in POC detection of the telomerase activity.
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