Deactivated Cas9-Engineered Magnetic Micromotors toward a Point-of-Care Digital Viral RNA Assay

环介导等温扩增 注意事项 纳米技术 计算机科学 数字聚合酶链反应 材料科学 生物系统 计算生物学 生物 DNA 遗传学 医学 聚合酶链反应 护理部 基因
作者
Younseong Song,Hyunji Park,Prudhvi Thirumalaraju,Niveditha Kovilakath,Joseph Hardie,Arafeh Bigdeli,Yingnan Bai,Shing-Wan Chang,Jungmin Yoo,Manoj Kumar Kanakasabapathy,Sungwan Kim,Juhyeon Chun,Hui Chen,Jonathan Z. Li,Athe Tsibris,Daniel R. Kuritzkes,Hadi Shafiee
出处
期刊:ACS Nano [American Chemical Society]
卷期号:19 (9): 8646-8660 被引量:5
标识
DOI:10.1021/acsnano.4c14913
摘要

Digital nucleic acid assays, known for their high sensitivity and specificity, typically rely on fluorescent readouts and expensive and complex nanowell manufacturing, which constrain their broader use in point-of-care (POC) application. Here, we introduce an alternative digital molecular diagnostics, termed dCRISTOR, by seamlessly integrating deactivated Cas9 (dCas9)-engineered micromotors, extraction-free loop-mediated isothermal amplification (LAMP), low-cost bright field microscopy, and deep learning-enabled image processing. The micromotor, composed of a polystyrene sphere attached to a magnetic bead, incorporates a dCas9 ribonucleoprotein complex. The presence of human immunodeficiency virus-1 (HIV-1) RNA in a sample results in the formation of large-sized amplicons that can be specifically captured by the micromotors, reducing their velocity induced by an external magnetic field. The micromotor is propelled by an external magnetic field, which eliminates the need for chemical fuels, reducing system complexity, and allowing for precise control over micromotor movement, enhancing accuracy and reliability. A convolutional neural network classification-based multiobject tracking algorithm, CNN-MOT, accurately measures the change in micromotor motion, facilitating the binary digital assay format ("1" or "0") for simplified result interpretation without user bias. Incorporating an extraction-free LAMP assay streamlines the dCRISTOR workflow, enabling qualitative HIV-1 detection in spiked plasma (n = 21) that demonstrates 100% sensitivity and specificity and achieves a limit of detection (LOD) of 0.96 copies/μL. The assay also achieved 100% correlation with reverse transcription-quantitative polymerase chain reaction (RT-qPCR) in clinical patient samples (n = 9). The dCRISTOR assay, a label-free digital nucleic acid testing system that eliminates the need for fluorescence readouts, absorbance measurements, or expensive manufacturing processes, represents a substantial advancement in digital viral RNA diagnostics.
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