SPRINT-Cas12a: A Single Leading-Hairpin Probe-Enabled Dual-Pathway Activation Strategy for Sensitive miRNA Detection

IF 7.3 1区 化学 Q1 CHEMISTRY, ANALYTICAL
Qian Li,Junda Liu,Mo Xue,Jiahao Wang,Youfei Zhang,Luzhen Huai,Xingzhou Zhu,Xiaoyan Liu,Jie Wang
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引用次数: 0

Abstract

CRISPR−Cas12a possesses robust trans-cleavage activity and has emerged as a powerful tool for nucleic acid detection. However, the efficient integration of Cas12a trans-cleavage with direct miRNA recognition and signal amplification remains challenging, particularly because conventional assay designs often rely on multiple probes or a single activation pathway. Here, we developed SPRINT-Cas12a, a single-probe RNA-triggered integrated trans-cleavage platform for sensitive miRNA detection. In this design, a leading hairpin probe (L-HP) specifically recognizes the target miRNA and initiates polymerase-mediated cascade isothermal amplification, synchronously generating two structurally distinct Cas12a-activating products: an RNA−DNA complex and a long-chain micro-hairpin probe (L-MHP). These products provide complementary activation pathways for Cas12a, thereby promoting reporter cleavage and fluorescence signal generation. The single-probe architecture simplifies probe design while enabling synergistic signal amplification through dual-pathway Cas12a activation. The platform was successfully adapted for the detection of miR-21 and miR-122, two miRNAs with distinct sequences, demonstrating its modularity and sequence versatility. Using miR-192 as a hepatocellular carcinoma-associated target, the method achieved sensitive detection in serum samples and distinguished patients with hepatocellular carcinoma from healthy controls, with results consistent with stem-loop quantitative reverse-transcription PCR. In addition, the platform was coupled with a lateral flow assay to provide an instrument-free visual readout. Depending on the amplification and readout format, the assay could be completed within 90 min to 120 min using simple laboratory equipment. Overall, SPRINT-Cas12a provides a single-probe, dual-pathway strategy for Cas12a-mediated miRNA detection and shows promise for portable molecular diagnostics and point-of-care testing.

Abstract Image

SPRINT-Cas12a:用于敏感miRNA检测的单导发夹探针双通路激活策略
CRISPR - Cas12a具有强大的反式切割活性,已成为核酸检测的有力工具。然而,Cas12a反式切割与直接miRNA识别和信号扩增的有效整合仍然具有挑战性,特别是因为传统的检测设计通常依赖于多个探针或单一激活途径。在这里,我们开发了SPRINT-Cas12a,这是一种单探针rna触发的集成反式切割平台,用于敏感的miRNA检测。在这个设计中,一个领先的发夹探针(L-HP)特异性识别目标miRNA并启动聚合酶介导的级联等温扩增,同步产生两个结构不同的cas12a激活产物:RNA - DNA复合物和长链微发夹探针(L-MHP)。这些产物为Cas12a提供了互补的激活途径,从而促进报告基因的裂解和荧光信号的产生。单探针结构简化了探针设计,同时通过双通路Cas12a激活实现了协同信号放大。该平台成功用于检测miR-21和miR-122这两种具有不同序列的mirna,证明了其模块化和序列通用性。利用miR-192作为肝细胞癌相关靶点,该方法在血清样本中实现了敏感检测,并将肝细胞癌患者与健康对照区分开来,结果与茎环定量反转录PCR一致。此外,该平台与横向流动分析相结合,提供无仪器的视觉读数。根据扩增和读出格式,使用简单的实验室设备,分析可在90分钟至120分钟内完成。总的来说,SPRINT-Cas12a为cas12a介导的miRNA检测提供了单探针、双途径策略,并有望用于便携式分子诊断和即时检测。
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来源期刊
Analytical Chemistry
Analytical Chemistry 化学-分析化学
CiteScore
12.10
自引率
12.20%
发文量
1949
审稿时长
1.4 months
期刊介绍: Analytical Chemistry, a peer-reviewed research journal, focuses on disseminating new and original knowledge across all branches of analytical chemistry. Fundamental articles may explore general principles of chemical measurement science and need not directly address existing or potential analytical methodology. They can be entirely theoretical or report experimental results. Contributions may cover various phases of analytical operations, including sampling, bioanalysis, electrochemistry, mass spectrometry, microscale and nanoscale systems, environmental analysis, separations, spectroscopy, chemical reactions and selectivity, instrumentation, imaging, surface analysis, and data processing. Papers discussing known analytical methods should present a significant, original application of the method, a notable improvement, or results on an important analyte.
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