The channel for RNA unwinding of NSP13 SARS-CoV-2 helicase is highly conserved in alpha and beta mammals coronavirus. Exploiting a funnel-like computational pipeline, we identified several micromolar or submicromolar NSP13 ligands blocking the central channel of NSP13. These compounds could potentially be good candidates for the development of a broad-spectrum drug for coronavirus infections.

Abstract

We have assembled a computational pipeline based on virtual screening, docking techniques, and nonequilibrium molecular dynamics simulations, with the goal of identifying possible inhibitors of the SARS-CoV-2 NSP13 helicase, catalyzing by ATP hydrolysis the unwinding of double or single-stranded RNA in the viral replication process inside the host cell. The druggable sites for broad-spectrum inhibitors are represented by the RNA binding sites at the 5’ entrance and 3’ exit of the central channel, a structural motif that is highly conserved across coronaviruses. Potential binders were first generated using structure-based ligand techniques. Their potency was estimated by using four popular docking scoring functions. Common docking hits for NSP13 were finally tested using advanced nonequilibrium alchemical techniques for binding free energy calculations on a high-performing parallel cluster. Four potential NSP13 inhibitors with potency from submicrimolar to nanomolar were finally identified.