ESCRT ubiquitin-binding domains function cooperatively during MVB cargo sorting

被引:85
作者
Shields, S. Brookhart [2 ]
Oestreich, Andrea J. [1 ]
Winistorfer, Stanley [2 ]
Nguyen, Doris [1 ]
Payne, Johanna A. [1 ]
Katzmann, David J. [1 ]
Piper, Robert [2 ]
机构
[1] Mayo Clin, Coll Med, Dept Biochem & Mol Biol, Rochester, MN 55905 USA
[2] Univ Iowa, Dept Mol Physiol & Biophys, Iowa City, IA 52240 USA
关键词
MULTIVESICULAR BODY PATHWAY; TSG101 UEV DOMAIN; VACUOLAR HYDROLASES; EAP45-GLUE DOMAIN; STRUCTURAL BASIS; COMPLEX; PROTEIN; YEAST; BODIES; RECOGNITION;
D O I
10.1083/jcb.200811130
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Ubiquitin (Ub) sorting receptors facilitate the targeting of ubiquitinated membrane proteins into multivesicular bodies (MVBs). Ub-binding domains (UBDs) have been described in several endosomal sorting complexes required for transport (ESCRT). Using available structural information, we have investigated the role of the multiple UBDs within ESCRTs during MVB cargo selection. We found a novel UBD within ESCRT-I and show that it contributes to MVB sorting in concert with the known UBDs within the ESCRT complexes. These experiments reveal an unexpected level of coordination among the ESCRT UBDs, suggesting that they collectively recognize a diverse set of cargo rather than act sequentially at discrete steps.
引用
收藏
页码:213 / 224
页数:12
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