Microvesicles are a source of contaminating cellular proteins found in purified HIV-1 preparations

被引:185
作者
Bess, JW
Gorelick, RJ
Bosche, WJ
Henderson, LE
Arthur, LO
机构
[1] AIDS Vaccine Program, SAIC, Natl. Cancer Inst.-Frederick C., Frederick
关键词
D O I
10.1006/viro.1997.8499
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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.
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页码:134 / 144
页数:11
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