{"title":"Graphene Oxide Nanofluidic Ion Channels with Two-Gene Rolling Circle Amplification for Ultrasensitive and Specific Detection of SARS-CoV-2","authors":"Meihua Lin, , , Mengyu Yang, , , Yuling Xiao, , , Jing Zhao, , , Zhiwei Shang, , , Xinyi Liu, , , Luping Wang, , , Jing Pan, , , Xiaoqing Yi, , , Xiaojin Zhang*, , and , Fan Xia, ","doi":"10.1021/acs.analchem.5c04178","DOIUrl":null,"url":null,"abstract":"<p >Rapid, sensitive, and specific detection of SARS-CoV-2 remains a critical challenge for early diagnosis and effective outbreak control. Here, we present a solid-state nanochannel biosensor integrated with two-gene rolling circle amplification (RCA) for the ultrasensitive and specific detection of SARS-CoV-2. In this system, target gene fragments initiate RCA to generate highly charged, three-dimensional DNA nanoflowers, which can effectively hybridize with the capture probes functionalized on the surface of the graphene oxide membranes. The accumulation of these nanostructures modulates the surface charge, significantly enhancing ion current signals through the nanochannels for highly sensitive electrical detection. The biosensor achieves detection limits of 0.3 fM for the S gene DNA fragment and 0.1 fM for the N gene DNA fragment. When applied to pseudovirus samples, the dual-gene RCA dramatically improves sensitivity and can detect SARS-CoV-2 pseudovirus at as low as a 10,000-fold dilution, corresponding to just 0.3 copies/μL of the S gene and 0.4 copies/μL of the N gene, which represents a 10-fold improvement over single-gene assays. By integrating nanofluidic sensing with programmable nucleic acid amplification, this label-free platform offers robust and specific SARS-CoV-2 detection with promising adaptability for diagnosing other pathogens.</p>","PeriodicalId":27,"journal":{"name":"Analytical Chemistry","volume":"97 40","pages":"22153–22163"},"PeriodicalIF":6.7000,"publicationDate":"2025-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Analytical Chemistry","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.analchem.5c04178","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Rapid, sensitive, and specific detection of SARS-CoV-2 remains a critical challenge for early diagnosis and effective outbreak control. Here, we present a solid-state nanochannel biosensor integrated with two-gene rolling circle amplification (RCA) for the ultrasensitive and specific detection of SARS-CoV-2. In this system, target gene fragments initiate RCA to generate highly charged, three-dimensional DNA nanoflowers, which can effectively hybridize with the capture probes functionalized on the surface of the graphene oxide membranes. The accumulation of these nanostructures modulates the surface charge, significantly enhancing ion current signals through the nanochannels for highly sensitive electrical detection. The biosensor achieves detection limits of 0.3 fM for the S gene DNA fragment and 0.1 fM for the N gene DNA fragment. When applied to pseudovirus samples, the dual-gene RCA dramatically improves sensitivity and can detect SARS-CoV-2 pseudovirus at as low as a 10,000-fold dilution, corresponding to just 0.3 copies/μL of the S gene and 0.4 copies/μL of the N gene, which represents a 10-fold improvement over single-gene assays. By integrating nanofluidic sensing with programmable nucleic acid amplification, this label-free platform offers robust and specific SARS-CoV-2 detection with promising adaptability for diagnosing other pathogens.
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.