De novo design of a stapled peptide targeting SARS-CoV-2 spike protein receptor-binding domain.

De novo design of a stapled peptide targeting SARS-CoV-2 spike protein receptor-binding domain.

Publication date: Sep 19, 2023

Although effective vaccines have been developed against SARS-CoV-2, many regions in the world still have low rates of vaccination and new variants with mutations in the viral spike protein have reduced the effectiveness of most available vaccines and treatments. There is an urgent need for a drug to cure this disease and prevent infection. The SARS-CoV-2 virus enters the host cell through protein-protein interaction between the virus’s spike protein and the host’s angiotensin converting enzyme (ACE2). Using protein design software and molecular dynamics simulations, we have designed a 17-residue peptide (pep39), that binds to the spike protein receptor-binding domain (RBD) and blocks interaction of spike protein with ACE2. We have confirmed the binding activity of the designed peptide for the original spike protein and the delta variant spike protein using micro-cantilever and bio-layer interferometry (BLI) based methods. We also confirmed that pep39 strongly inhibits SARS-CoV-2 virus replication in Vero E6 cells. Taken together these data suggest that a newly designed spike protein RBD blocking peptide pep39 has a potential as a SARS-CoV-2 virus inhibitor.

Concepts Keywords
Angiotensin Binding
Host Cov
Molecular Design
Pep39 Designed
Vaccines Domain
Host
Interaction
Pep39
Peptide
Protein
Receptor
Sars
Spike
Vaccines
Virus

Semantics

Type Source Name
disease VO effective
disease VO vaccination
disease VO effectiveness
disease MESH infection
disease IDO host
drug DRUGBANK Angiotensin II
disease IDO replication

Original Article

(Visited 1 times, 1 visits today)