Aptamer-based electrochemical biosensor with S protein binding affinity for COVID-19 detection: Integrating computational design with experimental validation of S protein binding affinity

Abstract

Aptamer-based biosensors capable of rapid one-step detection of viruses provide new capabilities for large-scale detection of COVID-19. Here we report a combined aptamer-based electrochemical and computational approach to characterize the interaction between a 60 base single stranded (ss)DNA aptamer and the viral S protein using molecular docking and bioinformatics tools. To construct the biosensor, the DNA aptamer was immobilized to the surface of a gold nanoparticles (AuNPs) modified electrode and methylene blue (MB) was used as redox indicator. Based on thermodynamic calculations for the aptamer sequence as well as several runs in APBS (Adaptive Poisson-Boltzmann Equation), we found that S protein GLN104-ASP115 pocket is the candidate for DNA 30–39(GGGAGTGGTT) sequence interaction. In the presence of S-protein, the target induced conformational changes in the aptamer’s structure, generating an increase in the MB redox signal, with a linear range between 10 pM to 6 nM and a limit of detection of 91.1 pM using differential pulse voltammetry (DPV). The aptasensor was investigated in spiked human saliva and serum samples, demonstrating performance in both media. This study demonstrates the potential of the MB-labeled electrochemical aptasensor for direct one-step detection of viral proteins, COVID-19 and potentially other viral agents.