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Updated: Jul 17, 2026

Studying the Stoichiometry of Epidermal Growth Factor Receptor in Intact Cells using Correlative Microscopy
Published on: September 11, 2015
Targeting of AMSH to endosomes is required for epidermal growth factor receptor degradation
Yu May Ma1, Emmanuel Boucrot1, Judit Villén2
1CBR Institute for Biomedical Research, Harvard Medical School, Boston, Massachusetts 02115; Department of Cell Biology, Harvard Medical School, Boston, Massachusetts 02115.
Abstract:
To reach the lysosomes, down-regulated receptors such as the epidermal growth factor receptor must first be sorted into internal vesicles of late endosomes (multivesicular bodies), a ubiquitin-dependent event that requires the coordinated function of the endosome sorting complex required for transport (ESCRT) proteins. Here we report that CHMP3, an ESCRT-III complex component, and associated molecule of SH3 domain of STAM (AMSH), a deubiquitinating enzyme, interact with each other in cells. A dominant-negative version of CHMP3, which specifically prevents targeting of AMSH to endosomes, inhibits degradation but not internalization of EGFR, suggesting that endosomal AMSH is a functional component of the multivesicular body pathway.
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