Vesiculovirus matrix proteins

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Vesiculovirus matrix (M) proteins are integral components of the Vesiculovirus genus within the family Rhabdoviridae, which includes viruses such as the Rabies virus and Vesicular stomatitis virus (VSV). These proteins play a crucial role in the virus life cycle, including virus assembly, budding, and pathogenesis. The M proteins are known for their ability to interact with multiple components of the host cell, thereby facilitating the efficient assembly and release of viral particles.

Function[edit | edit source]

The primary function of the Vesiculovirus M proteins is to mediate the assembly of virus particles and promote their budding from the host cell. They achieve this by interacting with the viral nucleocapsid and the host cell's plasma membrane, effectively bridging the gap between the two. This interaction is crucial for the encapsidation of the viral RNA genome and the formation of the viral envelope. Additionally, M proteins have been shown to play a role in inhibiting host antiviral responses, thereby aiding in the evasion of the host's immune system.

Structure[edit | edit source]

Vesiculovirus M proteins are small, basic proteins that possess the ability to bind to membranes. Their structure is characterized by a high degree of flexibility, which allows them to interact with various partners within the host cell. Despite their importance, the detailed structural information of these proteins is limited, and further studies are necessary to fully understand their mechanism of action.

Pathogenesis[edit | edit source]

The interaction of M proteins with host cell components is not only essential for virus assembly and release but also contributes to the pathogenicity of the virus. By inhibiting host antiviral responses, M proteins facilitate the sustained replication of the virus within the host. This mechanism is a key factor in the virulence of Vesiculoviruses.

Research and Implications[edit | edit source]

Research on Vesiculovirus M proteins has significant implications for understanding viral replication and pathogenesis. Insights into the interactions between M proteins and host cell components could lead to the development of novel antiviral strategies. Furthermore, the role of M proteins in immune evasion highlights their potential as targets for therapeutic intervention.

See Also[edit | edit source]


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Contributors: Prab R. Tumpati, MD