An all-in-one telomerase assay based on CRISPR-Cas12a trans-cleavage while telomere synthesis

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
出处
期刊:Analytica Chimica Acta [Elsevier BV]
卷期号:1159: 338404-338404 被引量:29
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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