Publication:
A density functional theory study on silver and bis-silver complexes with lighter tetrylene: are silver and bis-silver carbenes candidates for SARS-CoV-2 inhibition? Insight from molecular docking simulation
A density functional theory study on silver and bis-silver complexes with lighter tetrylene: are silver and bis-silver carbenes candidates for SARS-CoV-2 inhibition? Insight from molecular docking simulation
No Thumbnail Available
Files
Date
2020
Authors
Thanh Q. Bui
Huynh Thi Phuong Loan
Tran Thi Ai My
Duong Tuan Quang
Bui Thi Phuong Thuy
Vo Duy Nhan
Phan Tu Quy
Pham Van Tat
Duy Quang Dao
Nguyen Tien Trung
Journal Title
Journal ISSN
Volume Title
Publisher
Research Projects
Organizational Units
Journal Issue
Abstract
Ribavirin and remdesivir have been preclinically reported as potential drugs for the treatment of SARS-CoV-
2 infection, while light silver tetrylene complexes (NHEPh–AgCl and (NHEPh–AgCl)2 with E ¼ C, Si, and Ge)
have gained significant interest due to their promising applicability on the cytological scale. Firstly, the
structures and bonding states of silver–tetrylene complexes (NHE–Ag) and bis-silver–tetrylene
complexes (NHE–Ag-bis) were investigated using density functional theory (DFT) at the BP86 level with
the def2-SVP and def2-TZVPP basis sets. Secondly, the inhibitory capabilities of the carbene complexes
(NHC–Ag and NHC–Ag-bis) and the two potential drugs (ribavirin and remdesivir) on human-protein
ACE2 and SARS-CoV-2 protease PDB6LU7 were evaluated using molecular docking simulation. The
carbene ligand NHC bonds in a head-on configuration with AgCl and (AgCl)2, whereas, the other NHE (E
¼ Si and Ge) tetrylene ligands bond in a side-on mode to the metal fragments. The bond dissociation
energy (BDE) of the NHE–Ag bond in the complex families follows the order of NHC–Ag > NHSi–Ag >
NHGe–Ag and NHSi–Ag-bis > NHGe–Ag-bis > NHC–Ag-bis. The natural bond orbital analysis implies
that the [NHEPh/AgCl] and [(NHEPh)2/(AgCl)2] donations are derived mainly from the s- and pcontributions
of the ligands. The docking results indicate that both the ACE2 and PDB6LU7 proteins are
strongly inhibited by silver–carbene NHC–Ag, bis-silver–carbene NHC–Ag-bis, ribavirin, and remdesivir
with the docking score energy values varying from 17.5 to 16.5 kcal mol 1 and 16.9 to
16.6 kcal mol 1, respectively. The root-mean-square deviation values were recorded to be less than 2
A
in all the calculated systems. Thus, the present study suggests that silver–carbene NHC–Ag and bissilver–
carbene NHC–Ag-bis complexes are potential candidates to inhibit ACE2 and PDB6LU7, and thus
potentially conducive to prevent infection caused by the SARS-CoV-2 virus.