School of Medical Science, Menzies Health Institute Queensland, Griffith University (Gold Coast campus), Parklands Drive, Southport, QLD 4222, Australia.
School of Medical Science, Menzies Health Institute Queensland, Griffith University (Gold Coast campus), Parklands Drive, Southport, QLD 4222, Australia.
Int J Biol Macromol. 2019 Apr 15;127:1-11. doi: 10.1016/j.ijbiomac.2019.01.015. Epub 2019 Jan 4.
ESCRT (Endosomal Sorting Complex Required for Transport) machinery drives different cellular processes such as endosomal sorting, organelle biogenesis, vesicular trafficking, maintenance of plasma membrane integrity, membrane fission during cytokinesis and enveloped virus budding. The normal cycle of assembly and disassembly of some ESCRT complexes at the membrane requires the AAA-ATPase vacuolar protein sorting 4 (Vps4p). A number of ESCRT proteins are hijacked by clinically significant enveloped viruses including Ebola, and Human Immunodeficiency Virus (HIV) to enable enveloped virus budding and Vps4p provides energy for the disassembly/recycling of these ESCRT proteins. Several years ago, the failure of the terminal budding process of HIV following Vps4 protein inhibition was published; although at that time a detailed understanding of the molecular players was missing. However, later it was acknowledged that the ESCRT machinery has a role in enveloped virus budding from cells due to its role in the multivesicular body (MVB) sorting pathway. The MVB sorting pathway facilitates several cellular activities in uninfected cells, such as the down-regulation of signaling through cell surface receptors as well as the process of viral budding from infected host cells. In this review, we focus on summarising the functional organisation of ESCRT proteins at the membrane and the role of ESCRT machinery and Vps4p during MVB sorting and enveloped viral budding.
ESCRT(内体分选复合物必需的运输)机制驱动着不同的细胞过程,如内体分选、细胞器发生、囊泡运输、质膜完整性的维持、胞质分裂期间的膜裂变和包膜病毒出芽。一些 ESCRT 复合物在膜上的正常组装和拆卸循环需要 AAA-ATP 酶液泡蛋白分选 4(Vps4p)。许多 ESCRT 蛋白被临床上有意义的包膜病毒劫持,包括埃博拉病毒和人类免疫缺陷病毒(HIV),以实现包膜病毒出芽,Vps4p 为这些 ESCRT 蛋白的拆卸/回收提供能量。几年前,在 Vps4 蛋白抑制后,HIV 的末端出芽过程失败被发表;尽管当时对分子参与者缺乏详细的了解。然而,后来人们认识到 ESCRT 机制在细胞中包膜病毒出芽中起作用,因为它在多泡体(MVB)分选途径中的作用。MVB 分选途径促进未感染细胞中的几种细胞活动,如通过细胞表面受体的信号下调以及感染宿主细胞中病毒出芽的过程。在这篇综述中,我们重点总结了 ESCRT 蛋白在膜上的功能组织以及 ESCRT 机制和 Vps4p 在 MVB 分选和包膜病毒出芽中的作用。