Respiratory syncytial virus entry mechanism in host cells: A general overview

Author:

Cadena‐Cruz C.12ORCID,Villarreal Camacho J. L.2,De Ávila‐Arias Marcio1,Hurtado‐Gomez Leidy1,Rodriguez Alexander1,San‐Juan‐Vergara Homero1

Affiliation:

1. División Ciencias de la Salud Universidad del Norte Barranquilla Barranquilla Colombia

2. Facultad de Ciencias de la Salud, Programa de Medicina Universidad Libre Seccional Barranquilla Barranquilla Colombia

Abstract

AbstractRespiratory syncytial virus (RSV) is a virus that causes acute respiratory infections in neonates and older adults. To infect host cells, the attachment glycoprotein (G) interacts with a cell surface receptor. This interaction determines the specific cell types that are susceptible to infection. RSV possesses a type I fusion protein F. Type I fusion proteins are metastable when rearrangement of the prefusion F occurs; the fusion peptide is exposed transforming the protein into postfusion form. The transition between the prefusion form and its postfusion form facilitates the viral envelope and the host cell membrane to fuse, enabling the virus to enter the host cell. Understanding the entry mechanism employed by RSV is crucial for developing effective antiviral therapies. In this review, we will discuss the various types of viral fusion proteins and explore the potential entry mechanisms utilized by RSV. A deeper understanding of these mechanisms will provide valuable insights for the development of novel approaches to treat RSV infections.

Publisher

Wiley

Subject

Molecular Biology,Microbiology

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Structure-guided design of a trivalent nanobody cluster targeting SARS-CoV-2 spike protein;International Journal of Biological Macromolecules;2024-01

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