Rapid and Multiplexed Nucleic Acid Detection using Programmable Aptamer-Based RNA Switches
Yan, Z.; Tang, A. A.; Eshed, A.; Ticktin, Z. M.; Chaudhary, S.; Ma, D.; McCutcheon, G.; Li, Y.; Wu, K.; Saha, S.; Alcantar-Fernandez, J.; Moreno-Camacho, J. L.; Campos-Romero, A.; Collins, J. J.; Yin, P.; Green, A. A.
Show abstract
Rapid, simple, and low-cost diagnostic technologies are crucial tools for combatting infectious disease. Here, we describe a class of aptamer-based RNA switches called aptaswitches that recognize specific target nucleic acid molecules and respond by initiating folding of a reporter aptamer. Aptaswitches can detect virtually any sequence and provide a fast and intense fluorescent readout, generating signals in as little as 5 minutes and enabling detection by eye with minimal equipment. We demonstrate that aptaswitches can be used to regulate folding of six different fluorescent aptamer/fluorogen pairs, providing a general means of controlling aptamer activity and an array of different reporter colors for multiplexing. By coupling isothermal amplification reactions with aptaswitches, we reach sensitivities down to 1 RNA copy/{micro}L in one-pot reactions. Application of multiplexed one-pot reactions against RNA extracted from clinical saliva samples yields an overall accuracy of 96.67% for detection of SARS-CoV-2 in 30 minutes. Aptaswitches are thus versatile tools for nucleic acid detection that can be readily integrated into rapid diagnostic assays.
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