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Catalytic amplification by transition-state molecular switches for direct and sensitive detection of SARS-CoV-2

Despite the importance of nucleic acid testing in managing the COVID-19 pandemic, current detection approaches remain limited due to their high complexity and extensive processing. Here, we describe a molecular nanotechnology that enables direct and sensitive detection of viral RNA targets in native...

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Detalles Bibliográficos
Autores principales: Sundah, Noah R., Natalia, Auginia, Liu, Yu, Ho, Nicholas R. Y., Zhao, Haitao, Chen, Yuan, Miow, Qing Hao, Wang, Yu, Beh, Darius L. L., Chew, Ka Lip, Chan, Douglas, Tambyah, Paul A., Ong, Catherine W. M., Shao, Huilin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7968834/
https://www.ncbi.nlm.nih.gov/pubmed/33731349
http://dx.doi.org/10.1126/sciadv.abe5940
Descripción
Sumario:Despite the importance of nucleic acid testing in managing the COVID-19 pandemic, current detection approaches remain limited due to their high complexity and extensive processing. Here, we describe a molecular nanotechnology that enables direct and sensitive detection of viral RNA targets in native clinical samples. The technology, termed catalytic amplification by transition-state molecular switch (CATCH), leverages DNA-enzyme hybrid complexes to form a molecular switch. By ratiometric tuning of its constituents, the multicomponent molecular switch is prepared in a hyperresponsive state—the transition state—that can be readily activated upon the binding of sparse RNA targets to turn on substantial enzymatic activity. CATCH thus achieves superior performance (~8 RNA copies/μl), direct fluorescence detection that bypasses all steps of PCR (<1 hour at room temperature), and versatile implementation (high-throughput 96-well format and portable microfluidic assay). When applied for clinical COVID-19 diagnostics, CATCH demonstrated direct and accurate detection in minimally processed patient swab samples.