Journal
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 145, Issue 37, Pages 20214-20228Publisher
AMER CHEMICAL SOC
DOI: 10.1021/jacs.2c04835
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Funding
- NSF [CBET RAPID 20-27778]
- NIAAA [AA029348]
- NIDCR [DE030852]
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We propose a net-shaped DNA nanostructure design strategy for selective recognition and capture of intact SARS-CoV-2 virions, enabling the development of a rapid and inexpensive COVID-19 test. Furthermore, this strategy can be customized for tackling other viruses.
We present a net-shaped DNA nanostructure (called DNA Net herein) design strategy for selective recognition and high-affinity capture of intact SARS-CoV-2 virions through spatial pattern-matching and multivalent interactions between the aptamers (targeting wild-type spike-RED) positioned on the DNA Net and the trimeric spike glycoproteins displayed on the viral outer surface. Carrying a designer nanoswitch, the DNA Net-aptamers release fluorescence signals upon virus binding that are easily read with a handheld fluorimeter for a rapid (in 10 min), ature compatible, and inexpensive (similar to$1.26/test) COVID-19 test assay. The DNA Net-aptamers also impede authentic wild-type SARS-CoV-2 infection in cell culture with a near 1 x 10(3)-fold enhancement of the monomeric aptamer. Furthermore, our DNA Net design principle and strategy can be customized to tackle other life-threatening and economically influential viruses like influenza and HIV, whose surfaces carry class-I viral envelope glycoproteins like the SARS-CoV-2 spikes in trimeric forms.
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