Molecular Modelling, Synthesis, and In-Vitro Assay to Identify Potential Antiviral Peptides Targeting the 3-Chymotrypsin-Like Protease of SARS-CoV-2
by Faddis, R.; Du, S.; Stewart, J.; Hasan, M. M.; Lewit, N.; Ali, M. A.; White, C. B.; Okoto, P.; Thallapuranam, S.; Halim, M. A.
Chymotrypsin- like cysteine protease, also known as main protease (3CLpro/Mpro) of SARS-CoV-2, is highly conserved among various coronaviruses. Hence, therapeutics targeting the main protease are likely to show broad-spectrum activity. Peptides are a promising avenue for antiviral therapeutics as they are capable of offering a sustainable strategy to combat infectious diseases. In this work, we screened clinically proven antimicrobial peptides against the cysteine protease of SARSCoV-2 using state-of-the-art cheminformatics methods including docking and dynamics simulation, statistical analysis, and structure-activity relationship studies. From the molecular docking investigation, three peptides were chosen which showed the high binding affinities [DRAMP18152 (Delta G = - 56.56 kcal/mol), DRAMP18160 (Delta G = - 59.9 kcal/mol), DRAMP20773 (Delta G = - 56.2 kcal/mol)] and active interactions with His41 and Cys145 residues. Molecular dynamics simulation was employed over 250 ns on these three peptide-Mpro complexes. The MD simulation results reflect the high inhibitory potential of DRAMP18152, DRAMP18160, and DRAMP20773 against Mpro. These three peptides were synthesized using standard solid phase peptide synthesis. Purity (> 90%) and identity of the peptides were established by liquid chromatography and electrospray ionization-mass spectrometry. FRET-based protease assay was conducted for these three top candidates in which only DRAMP18160 showed the inhibition efficiency with an estimated 50% inhibitory concentrations of 59 mu M with low cytotoxicity. These results suggest that pursuing further development of peptide-based inhibitors for antiviral applications may be a fruitful endeavor and yield novel antiviral therapeutics. [GRAPHICS] .
- Journal
- International Journal of Peptide Research and Therapeutics
- Volume
- 29
- Issue
- 5
- Year
- 2023
- Start Page
- 13
- URL
- https://dx.doi.org/10.1007/s10989-023-10563-w
- ISBN/ISSN
- 1573-3904; 1573-3149
- DOI
- 10.1007/s10989-023-10563-w