Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, 575 Science Drive, Madison, WI 53711, USA.
J Virol. 2011 Apr;85(7):3631-41. doi: 10.1128/JVI.01984-10. Epub 2011 Jan 19.
During virus particle assembly, the arenavirus nucleoprotein (NP) associates with the viral genome to form nucleocapsids, which ultimately become incorporated into new virions at the cell membrane. Virion release is facilitated by the viral matrix Z protein through its interaction with the cellular endosomal sorting complex required for transport (ESCRT) machinery. However, the mechanism of nucleocapsid incorporation into virions is not well understood. Here, we demonstrate that ALIX/AIP1, an ESCRT-associated host protein, is required for the incorporation of the NP of Mopeia virus, a close relative of Lassa virus, into Z-induced virus-like particles (VLPs). Furthermore, we show that the Bro1 domain of ALIX/AIP1 interacts with the NP and Z proteins simultaneously, facilitating their interaction, and we identify residues 342 to 399 of NP as being necessary for its interaction with ALIX/AIP1. Our observations suggest a potential role for ALIX/AIP1 in linking Mopeia virus NP to Z and the budding apparatus, thereby promoting NP incorporation into virions.
在病毒粒子组装过程中,沙粒病毒核蛋白(NP)与病毒基因组结合形成核衣壳,最终在细胞膜处整合到新的病毒粒子中。病毒粒子的释放是通过病毒基质 Z 蛋白与细胞内必需的内体分选复合物(ESCRT)机制相互作用来促进的。然而,核衣壳整合到病毒粒子中的机制尚不清楚。在这里,我们证明了 ESCRT 相关宿主蛋白 AIP1/ALIX 对于 Mopeia 病毒(与 Lassa 病毒密切相关)NP 整合到 Z 诱导的病毒样颗粒(VLPs)中是必需的。此外,我们还表明,AIP1/ALIX 的 Bro1 结构域可以同时与 NP 和 Z 蛋白相互作用,促进它们之间的相互作用,并且我们确定 NP 的 342 到 399 个残基对于其与 AIP1/ALIX 的相互作用是必需的。我们的观察结果表明,AIP1/ALIX 可能在将 Mopeia 病毒 NP 与 Z 和出芽装置连接,从而促进 NP 整合到病毒粒子中发挥作用。