Department of Laboratory Medicine, Guangdong Provincial Key Laboratory of Precision Medical Diagnostics, Guangdong Provincial Key Laboratory of Single Cell Technology and Application, Nanfang Hospital, Southern Medical University, Guangzhou, 510515, P.R. China.
School of Medical Technology, Guangdong Medical University, Dongguan, 523808, China.
J Nanobiotechnology. 2024 Oct 5;22(1):602. doi: 10.1186/s12951-024-02831-8.
Rapid and sensitive nucleic acid detection is vital in disease diagnosis and therapeutic assessment. Herein, we propose a co-freezing localized CRISPR-Cas12a (CL-Cas12a) strategy for sensitive nucleic acid detection. The CL-Cas12a was obtained through a 15-minute co-freezing process, allowing the Cas12a/crRNA complex and hairpin reporter confined on the AuNPs surface with high load efficiency, for rapid sensing of nucleic acid with superior performance to other localized Cas12a strategies. This CL-Cas12a based platform could quantitatively detect targets down to 98 aM in 30 min with excellent specificity. Furthermore, the CL-Cas12a successful applied to detect human papillomavirus infection and human lung cancer-associated single-nucleotide mutations. We also achieved powerful signal amplification for imaging Survivin mRNA in living cells. These findings highlight the potential of CL-Cas12a as an effective tool for nucleic acid diagnostics and disease monitoring.
快速灵敏的核酸检测在疾病诊断和治疗评估中至关重要。在此,我们提出了一种共冷冻无试剂的局部 CRISPR-Cas12a(CL-Cas12a)策略,用于灵敏的核酸检测。CL-Cas12a 通过 15 分钟的共冷冻过程获得,允许 Cas12a/crRNA 复合物和发夹报告分子以高负载效率被限制在 AuNPs 表面上,用于快速感应核酸,性能优于其他局部 Cas12a 策略。该基于 CL-Cas12a 的平台可在 30 分钟内定量检测低至 98 aM 的靶标,具有优异的特异性。此外,CL-Cas12a 成功应用于检测人乳头瘤病毒感染和与人类肺癌相关的单核苷酸突变。我们还实现了对活细胞中 Survivin mRNA 进行成像的强大信号放大。这些发现突显了 CL-Cas12a 在核酸诊断和疾病监测方面的应用潜力。