Wilk T, Gowen B, Fuller S D
Structural Biology Programme, European Molecular Biology Laboratory, 69117 Heidelberg, Germany.
J Virol. 1999 Mar;73(3):1931-40. doi: 10.1128/JVI.73.3.1931-1940.1999.
Recently, it was shown that actin molecules are present in human immunodeficiency virus type 1 (HIV-1) particles. We have examined the basis for incorporation and the location of actin molecules within HIV-1 and murine retrovirus particles. Our results show that the retroviral Gag polyprotein is sufficient for actin uptake. Immunolabeling studies demonstrate that actin molecules localize to a specific radial position within the immature particle, clearly displaced from the matrix domain underneath the viral membrane but in proximity to the nucleocapsid (NC) domain of the Gag polyprotein. When virus or subviral Gag particles were disrupted with nonionic detergent, actin molecules remained associated with the disrupted particles. Actin molecules remained in a stable complex with the NC cleavage product (or an NC-RNA complex) after treatment of the disrupted HIV-1 particles with recombinant HIV-1 protease. In contrast, matrix and capsid molecules were released. The same result was obtained when mature HIV-1 particles were disrupted with detergent. Taken together, these results indicate that actin molecules are associated with the NC domain of the viral polyprotein.
最近的研究表明,肌动蛋白分子存在于1型人类免疫缺陷病毒(HIV-1)颗粒中。我们研究了HIV-1和鼠逆转录病毒颗粒中肌动蛋白分子的掺入基础及其位置。我们的结果表明,逆转录病毒Gag多聚蛋白足以摄取肌动蛋白。免疫标记研究表明,肌动蛋白分子定位于未成熟颗粒内特定的径向位置,明显偏离病毒膜下方的基质结构域,但靠近Gag多聚蛋白的核衣壳(NC)结构域。当病毒或亚病毒Gag颗粒用非离子去污剂破坏时,肌动蛋白分子仍与破坏后的颗粒相关联。在用重组HIV-1蛋白酶处理破坏后的HIV-1颗粒后,肌动蛋白分子与NC裂解产物(或NC-RNA复合物)保持稳定的复合物。相比之下,基质和衣壳分子被释放。用去污剂破坏成熟的HIV-1颗粒时也得到了相同的结果。综上所述,这些结果表明肌动蛋白分子与病毒多聚蛋白的NC结构域相关联。