Protein-Ligand Docking Simulations with AutoDock4 Focused on the Main Protease of SARS-CoV-2.

BACKGROUND

The main protease of SARS-CoV-2 (M) is one of the targets identified in SARS-CoV-2, the causative agent of COVID-19. The application of X-ray diffraction crystallography made available the three-dimensional structure of this protein target in complex with ligands, which paved the way for docking studies.

OBJECTIVE

Our goal here is to review recent efforts in the application of docking simulations to identify inhibitors of the M using the program AutoDock4.

METHODS

We searched PubMed to identify studies that applied AutoDock4 for docking against this protein target. We used the structures available for M to analyze intermolecular interactions and reviewed the methods used to search for inhibitors.

RESULTS

The application of docking against the structures available for the M found ligands with an estimated inhibition in the nanomolar range. Such computational approaches focused on the crystal structures revealed potential inhibitors of M that might exhibit pharmacological activity against SARS-CoV-2. Nevertheless, most of these studies lack the proper validation of the docking protocol. Also, they all ignored the potential use of machine learning to predict affinity.

CONCLUSION

The combination of structural data with computational approaches opened the possibility to accelerate the search for drugs to treat COVID-19. Several studies used AutoDock4 to search for inhibitors of M. Most of them did not employ a validated docking protocol, which lends support to critics of their computational methodology. Furthermore, one of these studies reported the binding of chloroquine and hydroxychloroquine to M. This study ignores the scientific evidence against the use of these antimalarial drugs to treat COVID-19.