Autophagy is a major pathway for the clearance of harmful material from the
cytoplasm. During autophagy, cytoplasmic material is delivered into the lysosomal
system by organelles called autophagosomes. Autophagosomes form in a de novo manner
and, in the course of their formation, isolate cargo material from the rest of the
cytoplasm. Cargo specificity is conferred by autophagic cargo receptors that
selectively link the cargo to the autophagosomal membrane decorated with ATG8 family
proteins such as LC3B. Here we show that the human cargo receptor p62/SQSTM-1 employs
oligomerization to stabilize its interaction with LC3B and linear ubiquitin when they
are clustered on surfaces. Thus, oligomerization enables p62 to simultaneously select
for the isolation membrane and the ubiquitinated cargo. We further show in a fully
reconstituted system that the interaction of p62 with ubiquitin and LC3B is
sufficient to bend the membrane around the cargo.DOI:
http://dx.doi.org/10.7554/eLife.08941.001
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.