ESCRT公司
内体
细胞生物学
生物
TSG101型
胞质分裂
脂质双层融合
溶酶体
膜泡运输蛋白质类
液泡
转运蛋白
内吞循环
液泡蛋白分选
微泡
内吞作用
细胞
细胞质
生物化学
细胞分裂
膜
细胞内
基因
小RNA
酶
作者
Christin Bissig,Jean Grüenberg
标识
DOI:10.1016/j.tcb.2013.10.009
摘要
In yeast and mammalian cells, endosomal sorting complexes required for transport (ESCRT) assist in sorting ubiquitinated proteins into intralumenal vesicles (ILVs) of multivesicular endosomes (MVEs) for degradation in the lysosome/vacuole. In mammalian cells, ESCRTs also drive other topologically identical membrane deformation processes, including cytokinesis, exosome release, and virus budding. Although the ESCRT-associated protein ALIX regulates these mammalian cell-specific functions, it was believed to be dispensable for receptor sorting into ILVs, unlike its yeast homolog Bro1. Despite these differences, recent evidence suggests ALIX and Bro1 share common properties in cargo sorting and ILV formation. We review these commonalities and discuss the role of ALIX in operating 'behind the mirror' during ILV back-fusion with the limiting membrane. We also propose models of how ALIX and some ESCRTs regulate the back-fusion process.
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