RT Journal Article
SR Electronic
T1 MMGB/SA Consensus Estimate of the Binding Free Energy Between the Novel Coronavirus Spike Protein to the Human ACE2 Receptor
JF bioRxiv
FD Cold Spring Harbor Laboratory
SP 2020.08.25.267625
DO 10.1101/2020.08.25.267625
A1 Negin Forouzesh
A1 Alexey V. Onufriev
YR 2020
UL http://biorxiv.org/content/early/2020/08/26/2020.08.25.267625.abstract
AB The ability to estimate protein-protein binding free energy in a computationally efficient via a physics-based approach is beneficial to research focused on the mechanism of viruses binding to their target proteins. Implicit solvation methodology may be particularly useful in the early stages of such research, as it can offer valuable insights into the binding process, quickly. Here we evaluate the potential of the related molecular mechanics generalized Born surface area (MMGB/SA) approach to estimate the binding free energy ΔGbind between the SARS-CoV-2 spike receptor-binding domain and the human ACE2 receptor. The calculations are based on a recent flavor of the generalized Born model, GBNSR6. Two estimates of ΔGbind are performed: one based on standard bondi radii, and the other based on a newly developed set of atomic radii (OPT1), optimized specifically for protein-ligand binding. We take the average of the resulting two ΔGbind values as the consensus estimate. For the well-studied Ras-Raf protein-protein complex, which has similar binding free energy to that of the SARS-CoV-2/ACE2 complex, the consensus ΔGbind = −11.8 ± 1 kcal/mol, vs. experimental −9.7 ± 0.2 kcal/mol.The consensus estimates for the SARS-CoV-2/ACE2 complex is ΔGbind = −9.4 ± 1.5 kcal/mol, which is in near quantitative agreement with experiment (−10.6 kcal/mol). The availability of a conceptually simple MMGB/SA-based protocol for analysis of the SARS-CoV-2 /ACE2 binding may be beneficial in light of the need to move forward fast.Competing Interest StatementThe authors have declared no competing interest.