Liu Li, Xu Zhiheng, Awayda Kamel, Dollery Stephen J, Bao Mengdi, Fan Jianlin, Cormier Denis, O'Connell Mitchell, Tobin Gregory J, Du Ke
Department of Microsystems Engineering, Rochester Institute of Technology, Rochester, NY 14623, USA.
Department of Mechanical Engineering, Rochester Institute of Technology, Rochester, NY 14623, USA.
Adv Mater Technol. 2022 Mar;7(3). doi: 10.1002/admt.202101550. Epub 2022 Jan 22.
A gold nanoparticle (AuNP) labeled CRISPR-Cas13a nucleic acid assay has been developed for sensitive solid-state nanopore sensing. Instead of directly detecting the translocation of RNA through a nanopore, our system utilizes non-covalent conjugates of AuNPs and RNA targets. Upon CRISPR activation, the AuNPs are liberated from the RNA, isolated, and passed through a nanopore sensor. Detection of the AuNPs can be observed as increasing ionic current in the chip. Each AuNP that is detected is enumerated as an event, leading to quantitative of molecular targets. Leveraging the high signal-to-noise ratio enabled by the AuNPs, a detection limit of 50 fM before front-end target amplification is achieved using SARS-CoV-2 RNA segments as a Cas13 target. Furthermore, a dynamic range of six orders of magnitude is demonstrated for quantitative RNA sensing. This simplified AuNP-based CRISPR assay is performed at the physiological temperature without relying on thermal cyclers. In addition, the nanopore reader is similar in size to a smartphone, making the assay system suitable for rapid and portable nucleic acid biomarker detection in either low-resource settings or hospitals.
一种用于灵敏固态纳米孔传感的金纳米颗粒(AuNP)标记的CRISPR-Cas13a核酸检测方法已经被开发出来。我们的系统并非直接检测RNA通过纳米孔的易位,而是利用AuNP与RNA靶标的非共价结合物。在CRISPR激活后,AuNP从RNA上释放出来,被分离并通过纳米孔传感器。AuNP的检测可通过芯片中离子电流的增加来观察。每一个被检测到的AuNP都被计为一个事件,从而实现分子靶标的定量。利用AuNP实现的高信噪比,以SARS-CoV-2 RNA片段作为Cas13靶标,在前端靶标扩增之前实现了50 fM的检测限。此外,还展示了用于定量RNA传感的六个数量级的动态范围。这种基于AuNP的简化CRISPR检测方法在生理温度下进行,无需依赖热循环仪。此外,纳米孔阅读器的尺寸与智能手机相似,使得该检测系统适用于在资源匮乏地区或医院进行快速、便携的核酸生物标志物检测。