Structural behavior of monomer of SARS-CoV-2 spike protein during initial stage of adsorption on graphene

• Type: Article in International Scientific Journal
• Date: 2021

Authors

Benkova, Z (Author) Other; Natalia N D S Cordeiro (Author) FCUP

Journal

The Journal is awaiting validation by the Administrative Services.

Title: MATERIALS TODAY CHEMISTRY

Vol. 22

ISSN: 2468-5194

Indexing

ISI Web of Knowledge - 6 Citations

Other information

Authenticus ID: P-00V-GTH

DOI: 10.1016/j.mtchem.2021.100572

Abstract (EN): Spike glycoprotein of the SARS-CoV-2 virus and its structure play a crucial role in the infections of cells containing angiotensin-converting enzyme 2 (ACE2) as well as in the interactions of this virus with surfaces. Protection against viruses and often even their deactivation is one of the great varieties of graphene applications. The structural changes of the non-glycosylated monomer of the spike glycoprotein trimer (denoted as S-protein in this work) triggered by its adsorption onto graphene at the initial stage are investigated by means of atomistic molecular dynamics simulations. The adsorption of the S protein happens readily during the first 10 ns. The shape of the S-protein becomes more prolate during the adsorption, but this trend, albeit less pronounced, is observed also for the freely relaxing S-protein in water. The receptor-binding domain (RBD) of the free and adsorbed S-protein manifests itself as the most rigid fragment of the whole S-protein. The adsorption even enhances the rigidity of the whole S-protein as well as its subunits. Only one residue of the RBD involved in the specific interactions with ACE2 during the cell infection is involved in the direct contact of the adsorbed S-protein with the graphene. The new intramolecular hydrogen bonds formed during the S-protein adsorption replace the S-protein-water hydrogen bonds; this trend, although less apparent, is observed also during the relaxation of the free S protein in water. In the initial phase, the secondary structure of the RBD fragment specifically interacting with ACE2 receptor is not affected during the S-protein adsorption onto the graphene.

Language: English

Type (Professor's evaluation): Scientific

No. of pages: 12