» Articles » PMID: 39402013

Viral Entry Mechanisms: the Role of Molecular Simulation in Unlocking a Key Step in Viral Infections

Overview
Journal FEBS Open Bio
Specialty Biology
Date 2024 Oct 14
PMID 39402013
Authors
Affiliations
Soon will be listed here.
Abstract

Viral infections are a major global health concern, affecting millions of people each year. Viral entry is one of the crucial stages in the infection process, but its details remain elusive. Enveloped viruses are enclosed by a lipid membrane that protects their genetic material and these viruses are linked to various human illnesses, including influenza, and COVID-19. Due to the advancements made in the field of molecular simulation, significant progress has been made in unraveling the dynamic processes involved in viral entry of enveloped viruses. Simulation studies have provided deep insight into the function of the proteins responsible for attaching to the host receptors and promoting membrane fusion (fusion proteins), deciphering interactions between these proteins and receptors, and shedding light on the functional significance of key regions, such as the fusion peptide. These studies have already significantly contributed to our understanding of this critical aspect of viral infection and assisted the development of effective strategies to combat viral diseases and improve global health. This review focuses on the vital role of fusion proteins in facilitating the entry process of enveloped viruses and highlights the contributions of molecular simulation studies to uncover the molecular details underlying their mechanisms of action.

Citing Articles

Structural Bioinformatics: exciting times in a rapidly evolving field.

Soares C, Lousa D FEBS Open Bio. 2025; 15(2):200-201.

PMID: 39895624 PMC: 11788741. DOI: 10.1002/2211-5463.13968.

References
1.
Legare S, Lague P . The influenza fusion peptide adopts a flexible flat V conformation in membranes. Biophys J. 2012; 102(10):2270-8. PMC: 3353013. DOI: 10.1016/j.bpj.2012.04.003. View

2.
Pabis A, Rawle R, Kasson P . Influenza hemagglutinin drives viral entry via two sequential intramembrane mechanisms. Proc Natl Acad Sci U S A. 2020; 117(13):7200-7207. PMC: 7132276. DOI: 10.1073/pnas.1914188117. View

3.
Valerio M, Mendonca D, Morais J, Buga C, Cruz C, Castanho M . Parainfluenza Fusion Peptide Promotes Membrane Fusion by Assembling into Oligomeric Porelike Structures. ACS Chem Biol. 2022; 17(7):1831-1843. PMC: 9295702. DOI: 10.1021/acschembio.2c00208. View

4.
Durrant J, Kochanek S, Casalino L, Ieong P, Dommer A, Amaro R . Mesoscale All-Atom Influenza Virus Simulations Suggest New Substrate Binding Mechanism. ACS Cent Sci. 2020; 6(2):189-196. PMC: 7048371. DOI: 10.1021/acscentsci.9b01071. View

5.
Sun X, Jayaraman A, Maniprasad P, Raman R, Houser K, Pappas C . N-linked glycosylation of the hemagglutinin protein influences virulence and antigenicity of the 1918 pandemic and seasonal H1N1 influenza A viruses. J Virol. 2013; 87(15):8756-66. PMC: 3719814. DOI: 10.1128/JVI.00593-13. View