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  2. Gp41 - Wikipedia

    en.wikipedia.org/wiki/Gp41

    Gp41 also known as glycoprotein 41 is a subunit of the envelope protein complex of retroviruses, including human immunodeficiency virus (HIV). Gp41 is a transmembrane protein that contains several sites within its ectodomain that are required for infection of host cells.

  3. Structure and genome of HIV - Wikipedia

    en.wikipedia.org/wiki/Structure_and_genome_of_HIV

    The genome and proteins of HIV (human immunodeficiency virus) have been the subject of extensive research since the discovery of the virus in 1983. [1] [2] "In the search for the causative agent, it was initially believed that the virus was a form of the Human T-cell leukemia virus (HTLV), which was known at the time to affect the human immune system and cause certain leukemias.

  4. HIV - Wikipedia

    en.wikipedia.org/wiki/HIV

    HIV can infect a variety of immune cells such as CD4 + T cells, macrophages, and microglial cells. HIV-1 entry to macrophages and CD4 + T cells is mediated through interaction of the virion envelope glycoproteins (gp120) with the CD4 molecule on the target cells' membrane and also with chemokine co-receptors. [26] [44]

  5. Nef (protein) - Wikipedia

    en.wikipedia.org/wiki/Nef_(protein)

    By down regulating cell surface expression of CD4 and Lck, Nef creates a narrow TCR response which likely optimizes HIV-1 viral production and generates a susceptible population of cells to further infect. Nef retargets kinase-active Lck away from the plasma membrane to early and recycling endosomes (RE) as well as the Trans-Golgi network (TGN).

  6. Lipid bilayer - Wikipedia

    en.wikipedia.org/wiki/Lipid_bilayer

    Phospholipids with certain head groups can alter the surface chemistry of a bilayer and can, for example, serve as signals as well as "anchors" for other molecules in the membranes of cells. [3] Just like the heads, the tails of lipids can also affect membrane properties, for instance by determining the phase of the bilayer.

  7. Pathophysiology of HIV/AIDS - Wikipedia

    en.wikipedia.org/wiki/Pathophysiology_of_HIV/AIDS

    The reason for the preferential loss of mucosal CD4 + T cells is that a majority of mucosal CD4 + T cells express the CCR5 coreceptor, whereas a small fraction of CD4 + T cells in the bloodstream do so. [5] HIV seeks out and destroys CCR5 expressing CD4 + cells during acute infection. A vigorous immune response eventually controls the infection ...

  8. HIV tropism - Wikipedia

    en.wikipedia.org/wiki/HIV_tropism

    HIV can infect a variety of cells such as CD4+ helper T-cells and macrophages that express the CD4 molecule on their surface. HIV-1 entry to macrophages and T helper cells is mediated not only through interaction of the virion envelope glycoproteins ( gp120 ) with the CD4 molecule on the target cells but also with its chemokine coreceptors.

  9. HIV vaccine development - Wikipedia

    en.wikipedia.org/wiki/HIV_vaccine_development

    Env is a protein on the HIV surface that enables to infect cells. Env extends from the surface of the HIV virus particle. The spike-shaped protein is "trimeric" — with 3 identical molecules, each with a cap-like region called glycoprotein 120 (gp120) and a stem called glycoprotein 41 (gp41) that anchors Env in the viral membrane.