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In Vitro Disassembly of Influenza A Virus Capsids by Gradient Centrifugation
Published on: March 27, 2016
Molecular mechanism of paramyxovirus budding
1Department of Microbiology and Immunology, University of Rochester Medical Center, 601 Elmwood Avenue, Box 672, Rochester, NY 14642, USA. toru_takimoto@urmc.rochester.edu
Abstract:
Components of paramyxoviruses are assembled at the plasma membrane of infected cells, and progeny viruses are formed by the budding process. Although the molecular mechanisms that drive budding (membrane curving and "pinching-off" reaction) are not well understood, the viral matrix (M) protein is thought to play a major role in the process. The M protein forms a dense layer tightly associated with the inner leaflet of the plasma membrane of infected cells. Expression of the M protein of some paramyxoviruses results in the formation and release of virus-like particles that contain the M protein; thus, in these viruses, the M protein alone can apparently trigger all steps required for the formation and release of virus-like particles. M also interacts specifically with viral envelope glycoproteins and nucleocapsids and is involved in directed transport of viral components to the budding site at the apical surface of polarized cells. In addition, protein-protein interactions between M and the cytoplasmic tail of viral glycoproteins and between M and the nucleocapsid affect the efficiency of virus production. The structural organization of the virion and the functions of the M protein clearly indicate that this protein orchestrates the budding of paramyxovirus.
Insights
The paramyxovirus matrix (M) protein orchestrates virus budding by organizing viral components at the plasma membrane. This essential viral protein alone can drive the formation and release of virus-like particles.
Area of Science:
- Virology
- Cell Biology
- Structural Biology
Background:
- Paramyxoviruses assemble at the plasma membrane, with progeny viruses forming via budding.
- The molecular mechanisms of viral budding, including membrane dynamics, are not fully understood.
- The viral matrix (M) protein is a key component implicated in paramyxovirus budding.
Purpose of the Study:
- To elucidate the role of the paramyxovirus matrix (M) protein in viral assembly and budding.
- To investigate the M protein's interactions with viral components and the host cell membrane.
- To understand how M protein drives the formation and release of virus-like particles.
Main Methods:
- Analysis of M protein expression and its association with the plasma membrane.
- Investigating M protein interactions with viral glycoproteins and nucleocapsids.
- Studying the formation of virus-like particles upon M protein expression.
Main Results:
- The M protein forms a dense layer on the inner leaflet of the plasma membrane.
- M protein expression alone can induce the formation and release of virus-like particles.
- M protein mediates interactions with glycoproteins and nucleocapsids, directing them to the budding site.
Conclusions:
- The paramyxovirus M protein plays a central, orchestrating role in the viral budding process.
- M protein's ability to induce virus-like particle formation highlights its critical function in assembly and release.
- Understanding M protein function is crucial for developing antiviral strategies against paramyxoviruses.
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