| Literature DB >> 31122169 |
Alf Håkon Lystad1, Sven R Carlsson2, Anne Simonsen1.
Abstract
The machinery that decorates autophagic membranes with lipid-conjugated LC3/GABARAP is not yet fully understood. We recently reported the purification of the full-length ATG12-ATG5-ATG16L1 complex, and in reconstitution experiments with purified ATG7, ATG3, and LC3/GABARAP in vitro, together with rescue experiments in knockout cells, important aspects of the complete lipidation reaction were revealed. Hitherto unobserved membrane-binding regions in ATG16L1 were found, contributing to properties that explain the crucial role of this protein in membrane targeting and LC3/GABARAP lipidation in macroautophagy/autophagy and other related processes.Entities:
Keywords: ATG16L1; Amphipathic helix; GABARAP; LAP; LC3; autophagy; endosome; lipidation; membrane
Year: 2019 PMID: 31122169 PMCID: PMC6613903 DOI: 10.1080/15548627.2019.1618100
Source DB: PubMed Journal: Autophagy ISSN: 1554-8627 Impact factor: 16.016