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Chinese Academy of Sciences Institutional Repositories Grid
Dual-Pathway Lateral Flow Assay for Rapid and Sensitive SARS-CoV-2 RNA Detection via CRISPR/Cas13a-Mediated SERS

文献类型:期刊论文

作者Joung, Younju4; Han, Do Kyoung3; Jang, Hyowon2; Kang, Taejoon2,5; Chen, Lingxin1; Choo, Jaebum4
刊名ACS SENSORS
出版日期2025-08-22
卷号10期号:8页码:6253-6262
关键词surface-enhanced Raman scattering lateral flow assaystrips dual-pathway CRISPR/Cas13a SARS-CoV-2
ISSN号2379-3694
DOI10.1021/acssensors.5c02084
通讯作者Chen, Lingxin(lxchen@yic.ac.cn) ; Choo, Jaebum(jbchoo@cau.ac.kr)
英文摘要Reverse transcription-polymerase chain reaction (RT-PCR) has been the gold standard for SARS-CoV-2 detection during the COVID-19 pandemic. However, its requirement for RNA-to-DNA conversion, reliance on centralized laboratory infrastructure, and lengthy turnaround times have limited its application in point-of-care (POC) settings. CRISPR/Cas13a-mediated lateral flow assays (LFAs) have emerged as promising alternatives for direct RNA analysis, yet their two-step workflows introduce procedural complexity and reduce sensitivity. To overcome these limitations, we developed a dual-pathway LFA strip based on surface-enhanced Raman scattering (SERS), which integrates CRISPR/Cas13a-mediated RNA cleavage and SERS detection into a single, portable platform. The device utilizes five vertically stacked paper layers with distinct geometries, enabling sequential CRISPR reaction and SERS quantification through two independent pathways. When tested with SARS-CoV-2 ORF1ab RNA targets, the system exhibited an 80-fold increase in sensitivity and a 10 min reduction in assay time compared to conventional fluorescence assays. Clinical validation using 18 samples (13 positives and 5 negatives) demonstrated high diagnostic accuracy, fully consistent with RT-PCR results. By unifying CRISPR-based RNA recognition and SERS signal amplification in a user-friendly format, this dual-pathway LFA strip offers a rapid, ultrasensitive, and practical diagnostic tool for infectious diseases in POC settings.
WOS关键词AMPLIFICATION
WOS研究方向Chemistry ; Science & Technology - Other Topics
语种英语
WOS记录号WOS:001559994000001
资助机构National Natural Science Foundation of China ; National Research Foundation of Korea ; Technology Innovation Program ; Ministry of Trade, Industry, and Energy (MOTIE, Korea) ; National Nature Science Foundation of China ; Korea Basic Science Institute ; KRIBB Research Initiative Program
源URL[http://ir.yic.ac.cn/handle/133337/40796]  
专题烟台海岸带研究所_中科院海岸带环境过程与生态修复重点实验室
通讯作者Chen, Lingxin; Choo, Jaebum
作者单位1.Chinese Acad Sci, Yantai Inst Coastal Zone Res, Key Lab Coastal Environm Proc & Ecol Remediat, Yantai 264003, Peoples R China
2.Korea Res Inst Biosci & Biotechnol, Bionanotechnol Res Ctr, Daejeon 34141, South Korea
3.Korea Basic Sci Inst, Div Mat Anal & Res, Daejeon 34133, South Korea
4.Chung Ang Univ, Dept Chem, Seoul 06974, South Korea
5.Sungkyunkwan Univ, Sch Pharm, Suwon 16419, South Korea
推荐引用方式
GB/T 7714
Joung, Younju,Han, Do Kyoung,Jang, Hyowon,et al. Dual-Pathway Lateral Flow Assay for Rapid and Sensitive SARS-CoV-2 RNA Detection via CRISPR/Cas13a-Mediated SERS[J]. ACS SENSORS,2025,10(8):6253-6262.
APA Joung, Younju,Han, Do Kyoung,Jang, Hyowon,Kang, Taejoon,Chen, Lingxin,&Choo, Jaebum.(2025).Dual-Pathway Lateral Flow Assay for Rapid and Sensitive SARS-CoV-2 RNA Detection via CRISPR/Cas13a-Mediated SERS.ACS SENSORS,10(8),6253-6262.
MLA Joung, Younju,et al."Dual-Pathway Lateral Flow Assay for Rapid and Sensitive SARS-CoV-2 RNA Detection via CRISPR/Cas13a-Mediated SERS".ACS SENSORS 10.8(2025):6253-6262.

入库方式: OAI收割

来源:烟台海岸带研究所

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