tetano
Editor, Senior Moderator
Pathogens
. 2022 Feb 11;11(2):238.
doi: 10.3390/pathogens11020238.
The pH Effects on SARS-CoV and SARS-CoV-2 Spike Proteins in the Process of Binding to hACE2
Yixin Xie[SUP] 1 [/SUP], Wenhan Guo[SUP] 1 [/SUP], Alan Lopez-Hernadez[SUP] 1 [/SUP], Shaolei Teng[SUP] 2 [/SUP], Lin Li[SUP] 1 3 [/SUP]
Affiliations
Abstract
COVID-19 has been threatening human health since the late 2019, and has a significant impact on human health and economy. Understanding SARS-CoV-2 and other coronaviruses is important to develop effective treatments for COVID-19 and other coronavirus-caused diseases. In this work, we applied multi-scale computational approaches to study the electrostatic features of spike (S) proteins for SARS-CoV and SARS-CoV-2. From our results, we found that SARS-CoV and SARS-CoV-2 have similar charge distributions and electrostatic features when binding with the human angiotensin-converting enzyme 2 (hACE2). Energy pH-dependence calculations revealed that the complex structures of hACE2 and the S proteins of SARS-CoV/SARS-CoV-2 are stable at pH values ranging from 7.5 to 9. Three independent 100 ns molecular dynamics (MD) simulations were performed using NAMD to investigate the hydrogen bonds between S proteins RBD and hACE2 RBD. From MD simulations, we found that SARS-CoV-2 forms 19 pairs (average of three simulations) of hydrogen bonds with high occupancy (>50%) to hACE2, compared to 16 pairs between SARS-CoV and hACE2. Additionally, SARS-CoV viruses prefer sticking to the same hydrogen bond pairs, while SARS-CoV-2 tends to have a larger range of selections on hydrogen bonds acceptors. We also labelled key residues involved in forming the top five hydrogen bonds that were found in all three independent 100 ns simulations. This identification is important to potential drug designs for COVID-19 treatments. Our work will shed the light on current and future coronavirus-caused diseases.
Keywords: Angiotensin-Converting Enzyme 2; COVID-19; SARS-CoV; SARS-CoV-2; binding energy; electrostatic features; folding energy; hACE2; hydrogen bonds; pH dependence; spike protein.
. 2022 Feb 11;11(2):238.
doi: 10.3390/pathogens11020238.
The pH Effects on SARS-CoV and SARS-CoV-2 Spike Proteins in the Process of Binding to hACE2
Yixin Xie[SUP] 1 [/SUP], Wenhan Guo[SUP] 1 [/SUP], Alan Lopez-Hernadez[SUP] 1 [/SUP], Shaolei Teng[SUP] 2 [/SUP], Lin Li[SUP] 1 3 [/SUP]
Affiliations
- PMID: 35215181
- DOI: 10.3390/pathogens11020238
Abstract
COVID-19 has been threatening human health since the late 2019, and has a significant impact on human health and economy. Understanding SARS-CoV-2 and other coronaviruses is important to develop effective treatments for COVID-19 and other coronavirus-caused diseases. In this work, we applied multi-scale computational approaches to study the electrostatic features of spike (S) proteins for SARS-CoV and SARS-CoV-2. From our results, we found that SARS-CoV and SARS-CoV-2 have similar charge distributions and electrostatic features when binding with the human angiotensin-converting enzyme 2 (hACE2). Energy pH-dependence calculations revealed that the complex structures of hACE2 and the S proteins of SARS-CoV/SARS-CoV-2 are stable at pH values ranging from 7.5 to 9. Three independent 100 ns molecular dynamics (MD) simulations were performed using NAMD to investigate the hydrogen bonds between S proteins RBD and hACE2 RBD. From MD simulations, we found that SARS-CoV-2 forms 19 pairs (average of three simulations) of hydrogen bonds with high occupancy (>50%) to hACE2, compared to 16 pairs between SARS-CoV and hACE2. Additionally, SARS-CoV viruses prefer sticking to the same hydrogen bond pairs, while SARS-CoV-2 tends to have a larger range of selections on hydrogen bonds acceptors. We also labelled key residues involved in forming the top five hydrogen bonds that were found in all three independent 100 ns simulations. This identification is important to potential drug designs for COVID-19 treatments. Our work will shed the light on current and future coronavirus-caused diseases.
Keywords: Angiotensin-Converting Enzyme 2; COVID-19; SARS-CoV; SARS-CoV-2; binding energy; electrostatic features; folding energy; hACE2; hydrogen bonds; pH dependence; spike protein.