Influence of Cholesterol on the Insertion and Interaction of SARS-CoV-2 Proteins with Lipid Membranes
Open Access
- 6 June 2025
- journal article
- Published by American Chemical Society (ACS) in ACS Applied Bio Materials
- Vol. 8 (6) , 5380-5394
Abstract
Cholesterol is an essential sterol in cell membranes that regulates organization and fluidity. This biomolecule has been identified as one of the critical factors in the internalization process of various viruses in human cells. Therefore, understanding these mechanisms is crucial for a deeper comprehension of viral pathogenicity in the search for practical therapeutic approaches against viral diseases. The biochemical and biophysical processes related to these diseases are highly complex. For this reason, studying model systems capable of mimicking the interaction of lipid membranes with cholesterol and proteins is fundamental. In this work, we propose to study the structural and elastic changes in mono-, bi-, and tridimensional lipid systems composed of dipalmitoylphosphatidylcholine (PC) with varying amounts of cholesterol in the presence and absence of the S protein (Spike) and its receptor-binding domain (RBD) from SARS-CoV-2. To characterize these systems, we used both experimental and theoretical approaches such as Langmuir trough, atomic force microscopy (AFM), small-angle X-ray scattering (SAXS), electrochemical methods, and molecular dynamics (MD) simulations. With the interpretation of all results obtained in this work, it was possible to propose a structural model of the membrane in the presence of cholesterol and the interaction with the Spike protein and RBD. The behavior of the adsorption isotherm and SAXS data, together with the results provided by MD simulations, led us to conclude that cholesterol in PC monolayers promotes local alterations, inducing the formation of more rigid membrane regions. More importantly, cholesterol plays a crucial role in facilitating the allocation of SARS-CoV-2 proteins in lipid systems. This is especially true for the Spike protein, which displayed a non-ACE2 mediated stable binding to the lipid membrane with high internalization.Keywords
Funding Information
- Conselho Nacional de Desenvolvimento Cient?fico e Tecnol?gico (305574/2023-0, 382612/2022-1, 465389/2014-7)
- Funda??o de Amparo ? Pesquisa do Estado de S?o Paulo (2014/50867-3, 2017/02317-2, 2022/14753-0)
- Programa de Desarrollo de las Ciencias B?sicas
This publication has 67 references indexed in Scilit:
- Giant Plasma Membrane Vesicles as Cellular‐Mimics for Probing SARS‐CoV‐2 Binding at Single Particle LevelChemistrySelect, 2023
- Effect of γ-Oryzanol on the LE–LC Phase Coexistence Region of DPPC Langmuir MonolayerThe Journal of Membrane Biology, 2023
- Extracellular vesicles over adeno-associated viruses: Advantages and limitations as drug delivery platforms in precision medicineAdvanced Drug Delivery Reviews, 2022
- Spatial arrangement of proteins in planar and curved membranes by PPM 3.0Protein Science, 2021
- Synergy in the interaction of amoxicillin and methylene blue with dipalmitoyl phosphatidyl choline (DPPC) monolayersApplied Surface Science, 2019
- High Cholesterol/Low Cholesterol: Effects in Biological Membranes: A ReviewCell Biochemistry and Biophysics, 2017
- CHARMM36 all-atom additive protein force field: Validation based on comparison to NMR dataJournal of Computational Chemistry, 2013
- CHARMM‐GUI: A web‐based graphical user interface for CHARMMJournal of Computational Chemistry, 2008
- G-Protein-Coupled Receptor-Signaling Components in Membrane Raft and Caveolae Microdomains2008
- VMD: Visual molecular dynamicsJournal of Molecular Graphics, 1996