Env (gene)

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Env (short for envelope) is a gene found in retroviruses that encodes the viral envelope protein. This protein is crucial for the virus's ability to infect host cells. The Env gene is a key component in the life cycle of retroviruses, including the Human Immunodeficiency Virus (HIV) and the Human T-lymphotropic virus (HTLV).

Structure and Function[edit | edit source]

The Env gene encodes a precursor protein known as gp160 in HIV, which is subsequently cleaved into two subunits: gp120 and gp41. These subunits form a complex that is essential for the virus's ability to bind to and enter host cells.

  • gp120: This subunit is responsible for binding to the CD4 receptor on the surface of T cells, macrophages, and dendritic cells. The interaction between gp120 and the CD4 receptor is the first step in the viral entry process.
  • gp41: This subunit facilitates the fusion of the viral membrane with the host cell membrane, allowing the viral RNA to enter the host cell.

Role in Viral Entry[edit | edit source]

The Env protein mediates the initial attachment of the virus to the host cell. After gp120 binds to the CD4 receptor, it undergoes a conformational change that allows it to interact with a co-receptor, typically CCR5 or CXCR4. This interaction triggers further conformational changes in gp41, leading to the fusion of the viral and cellular membranes.

Genetic Variability[edit | edit source]

The Env gene is highly variable, which poses a significant challenge for the development of vaccines and treatments. The high mutation rate of the Env gene allows the virus to evade the host's immune system by altering its surface proteins.

Clinical Significance[edit | edit source]

The Env protein is a major target for antiretroviral therapy and vaccine development. Inhibitors that block the interaction between gp120 and the CD4 receptor, or that prevent the fusion process mediated by gp41, are being actively researched.

Research and Development[edit | edit source]

Ongoing research aims to develop effective vaccines that can elicit a strong immune response against the Env protein. Additionally, monoclonal antibodies targeting gp120 and gp41 are being explored as potential therapeutic agents.

See Also[edit | edit source]

References[edit | edit source]

External Links[edit | edit source]


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Contributors: Prab R. Tumpati, MD