化学
判别式
反式激活crRNA
小RNA
计算生物学
纳米技术
生物系统
色谱法
人工智能
生物化学
清脆的
材料科学
生物
计算机科学
回文
基因
作者
Xinyi Xia,Zhigang Liang,Guanhong Xu,Fangdi Wei,Jing Yang,Xiaolei Zhu,Chenglin Zhou,Jun Ye,Qin Hu,Zheng Zhao,Ben Zhong Tang,Yao Cen
标识
DOI:10.1021/acs.analchem.4c05388
摘要
Multiple sclerosis (MS) can proceed into secondary progressive MS accompanied by persistent neurological deterioration; therefore, accurate diagnosis of MS is of vital significance. Irregularities of microRNAs (miRNAs) expression have been observed in MS, so miRNAs have been evaluated as novel biomarkers and therapeutic targets. Herein, a new strategy named split crRNA precisely assisted Cas12a expansion (SPACE) was developed for simultaneous, discriminative, and low-threshold determination of two MS-related miRNAs: miRNA-155 and miRNA-326. On the one hand, owing to the property that split crRNA could activate Cas12a, miRNAs were designed as the spacers of crRNA to combine with scaffold. These integrated crRNAs then recognized the activators, activating Cas12a and enabling RNA target identification. On the other hand, the SPACE strategy dexterously integrated the activator with reporter probe, and utilized Cas12a′s cis-cleavage to achieve simultaneous detection and differential signal output for miRNA-155 and miRNA-326. Moreover, trans-cleavage with ultra-high efficiency was assembled in the SPACE strategy to achieve sensitive quantification of total miRNAs in blood samples at low thresholds. Overall, the diversified and integrated design of the SPACE strategy enabled simultaneous, discriminative, and low-threshold detection of dual MS-related miRNAs in one pot and one step, providing a reliable and accurate Cas12a detection tool for clinical low-threshold diagnosis.
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