Göttlinger H G, Dorfman T, Cohen E A, Haseltine W A
Division of Human Retrovirology, Dana-Farber Cancer Institute, Boston, MA 02115.
Proc Natl Acad Sci U S A. 1993 Aug 1;90(15):7381-5. doi: 10.1073/pnas.90.15.7381.
The Vpu protein of human immunodeficiency virus type 1 facilitates the release of virus particles from the surface of infected cells. The ability of the Vpu protein to facilitate release of Gag proteins from retroviruses that lack a Vpu-like protein was examined. The results of these experiments show that Vpu significantly increases the release of the Gag proteins of human immunodeficiency virus type 2, visna virus, and Moloney murine leukemia virus from HeLa cells. The results indicate that Vpu-mediated enhancement of particle release requires neither amino-terminal myristoylation of the Gag precursor nor cleavage of the Gag precursor by the viral protease. The results raise the possibility that Vpu modifies a cellular pathway common to the release of all retroviruses from the cell surface.
人类免疫缺陷病毒1型的Vpu蛋白有助于病毒颗粒从受感染细胞表面释放。研究了Vpu蛋白促进缺乏类似Vpu蛋白的逆转录病毒释放Gag蛋白的能力。这些实验结果表明,Vpu显著增加了人类免疫缺陷病毒2型、维斯纳病毒和莫洛尼鼠白血病病毒的Gag蛋白从HeLa细胞中的释放。结果表明,Vpu介导的颗粒释放增强既不需要Gag前体的氨基末端肉豆蔻酰化,也不需要病毒蛋白酶对Gag前体的切割。这些结果增加了Vpu修饰细胞从细胞表面释放所有逆转录病毒所共有的途径的可能性。