Net-Shaped DNA Nanostructures Designed for Rapid/Sensitive Detection and Potential Inhibition of the SARS-CoV-2 Virus.
Neha ChauhanYanyu XiongShaokang RenAbhisek DwivedyNicholas MagazineLifeng ZhouXiaohe JinTianyi ZhangBrian T CunninghamSherwood YaoWeishan HuangXing WangPublished in: Journal of the American Chemical Society (2022)
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-RBD) 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), simple (mix-and-read), sensitive (PCR equivalent), room temperature compatible, and inexpensive (∼$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 × 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.
Keyphrases
- sars cov
- single molecule
- circulating tumor
- cell free
- nucleic acid
- sensitive detection
- respiratory syndrome coronavirus
- wild type
- room temperature
- circulating tumor cells
- hiv infected
- human immunodeficiency virus
- gold nanoparticles
- antiretroviral therapy
- hiv aids
- hiv positive
- drug delivery
- cystic fibrosis
- transcription factor