4.4 Article

Binding to Any ESCRT Can Mediate Ubiquitin-Independent Cargo Sorting

期刊

TRAFFIC
卷 15, 期 2, 页码 212-229

出版社

WILEY-BLACKWELL
DOI: 10.1111/tra.12135

关键词

ESCRT; Multivesicular bodies; soluble MVB cargo; ubiquitin-independent cargo sorting

资金

  1. NIH [R01 GM074171]
  2. NSF-DMS [1122297]
  3. Direct For Mathematical & Physical Scien
  4. Division Of Mathematical Sciences [1160432] Funding Source: National Science Foundation
  5. Division Of Mathematical Sciences
  6. Direct For Mathematical & Physical Scien [1148230, 1122297] Funding Source: National Science Foundation

向作者/读者索取更多资源

The ESCRT (endosomal sorting complex required for transport) machinery is known to sort ubiquitinated transmembrane proteins into vesicles that bud into the lumen of multivesicular bodies (MVBs). Although the ESCRTs themselves are ubiquitinated they are excluded from the intraluminal vesicles and recycle back to the cytoplasm for further rounds of sorting. To obtain insights into the rules that distinguish ESCRT machinery from cargo we analyzed the trafficking of artificial ESCRT-like protein fusions. These studies showed that lowering ESCRT-binding affinity converts a protein from behaving like ESCRT machinery into cargo of the MVB pathway, highlighting the close relationship between machinery and the cargoes they sort. Furthermore, our findings give insights into the targeting of soluble proteins into the MVB pathway and show that binding to any of the ESCRTs can mediate ubiquitin-independent MVB sorting.

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