Rapid one-pot isothermal amplification reassembled of fluorescent RNA aptamer for SARS-CoV-2 detection.

Rapid one-pot isothermal amplification reassembled of fluorescent RNA aptamer for SARS-CoV-2 detection.

Publication date: Aug 15, 2024

The outbreak of SARS-CoV-2 poses a serious threat to human life and health. A rapid nucleic acid tests can effectively curb the spread of the disease. With the advantages of fluorescent RNA aptamers, low background and high sensitivity. A variety of fluorescent RNA aptamer sensors have been developed for the detection of nucleic acid. Here, we report a hypersensitive detection platform in which SARS-CoV-2 initiates RTF-EXPAR to amplify trigger fragments. This activation leads to the reassembled of the SRB2 fluorescent RNA aptamer, restoring its secondary structure for SR-DN binding and turn-on fluorescence. The platform completes the assay in 30 min and all reactions occur in one tube. The detection limit is as low as 116 aM. Significantly, the platform’s quantitative analyses were almost identical to qPCR results in simulated tests of positive samples. In conclusion, the platform is sensitive, accurate and provides a new protocol for point-of-care testing of viruses.

Concepts Keywords
30min Aptamers, Nucleotide
Fluorescence Aptamers, Nucleotide
Isothermal COVID-19
Tests Fluorescent Dyes
Viruses Fluorescent Dyes
Fluorescent RNA aptamer
Humans
Limit of Detection
One-pot
POCT
Reassembly
RNA, Viral
RNA, Viral
RTF-EXPAR
SARS-CoV-2

Semantics

Type Source Name
disease VO report
disease IDO assay
disease VO protocol
disease VO Viruses
disease MESH COVID-19

Original Article

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