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Microvesicles Are a Source of Contaminating Cellular Proteins Found in Purified Hiv-1 Preparations

  1. Author:
    Bess, J. W.
    Gorelick, R. J.
    Bosche, W. J.
    Henderson, L. E.
    Arthur, L. O.
  2. Author Address

    Bess JW NCI FREDERICK CANC RES & DEV CTR AIDS VACCINE PROGRAM SAIC FREDERICK, MD 21702 USA
    1. Year: 1997
  1. Journal: Virology
    1. 230
    2. 1
    3. Pages: 134-144
  2. Type of Article: Article
  1. Abstract:

    Identification and quantitation of cellular proteins associated with HIV-1 particles are complicated by the presence of nonvirion-associated cellular proteins that copurify with virions. Many cellular proteins are associated with nonviral particles that bud from the surface of cells called microvesicles. Microvesicles band in sucrose gradients in a range of densities that includes the same density as retroviruses. To characterize these microvesicles, HIV-1-infected and uninfected human T-cell lines were propagated and Virus and microvesicles were purified from clarified cell culture supernatants by sucrose density gradient centrifugation or centrifugation through 20% sucrose pads. Microvesicles were found to contain Various proteins, including HLA DR and beta 2-M, and a substantial amount of RNA and DNA The concentrations of HIV-1 p24(CA), HLA DR, and beta 2-microglobulin (beta 2-M) were determined by radioimmunoassay. The ratios of HIV-1 p24(CA) to HLA DR and beta 2-M were found to vary with respect to the HIV-1 isolate, host cell, and other factors. Electron microscopic analysis of microvesicles revealed that they consisted of particles of various sizes and morphologies. Although HIV-1 particles are known to contain some cellular proteins, microvesicles from HIV-1 infected H9 cells appeared to contain little or no HIV-1 gp120(SU). (C) 1997 Academic Press. [References: 46]

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