Amplification- and Enzyme-Free Magnetic Diagnostics Circuit for Whole-Genome Detection of SARS-CoV-2 RNA.
Enja Laureen RöschRebecca SackMohammad Suman ChowdhuryFlorian WolgastMargarete ZaborskiFrank LudwigMeinhard SchillingThilo ViereckUlfert RandAidin LakPublished in: Chembiochem : a European journal of chemical biology (2024)
Polymerase chain reaction (PCR) requires thermal cycling and enzymatic reactions for sequence amplification, hampering their applications in point-of-care (POC) settings. Magnetic bioassays based on magnetic particle spectroscopy (MPS) and magnetic nanoparticles (MNPs) are isothermal, wash-free, and can be quantitative. Realizing them amplification- and enzyme-free on a benchtop device, they will become irreplaceable for POC applications. Here we demonstrate a first-in-class magnetic signal amplification circuit (MAC) that enables detection of whole genome of SARS-CoV-2 by combining the specificity of toehold-mediated DNA strand displacement with the magnetic response of MNPs to declustering processes. Using MAC, we detect the N gene of SARS-CoV-2 samples at a concentration of 10 4 RNA copies/μl as determined by droplet digital PCR. Further, we demonstrate that MAC can reliably distinguish between SARS-CoV-2 and other human coronaviruses. Being a wash-, amplification- and enzyme-free biosensing concept and working at isothermal conditions (25 °C) on a low-cost benchtop MPS device, our MAC biosensing concept offers several indispensable features for translating nucleic acid detection to POC applications.
Keyphrases
- nucleic acid
- sars cov
- molecularly imprinted
- label free
- real time pcr
- respiratory syndrome coronavirus
- low cost
- loop mediated isothermal amplification
- magnetic nanoparticles
- endothelial cells
- high resolution
- genome wide
- single molecule
- gene expression
- high intensity
- mass spectrometry
- copy number
- nitric oxide
- solid phase extraction
- single cell
- quantum dots
- liquid chromatography
- sensitive detection
- solid state
- amino acid