| Literature DB >> 26995697 |
Nora Kory1, Robert V Farese2, Tobias C Walther3.
Abstract
How proteins specifically localize to the phospholipid monolayer surface of lipid droplets (LDs) is being unraveled. We review here the major known pathways of protein targeting to LDs and suggest a classification framework based on the localization origin for the protein. Class I proteins often have a membrane-embedded, hydrophobic 'hairpin' motif, and access LDs from the endoplasmic reticulum (ER) either during LD formation or after formation via ER-LD membrane bridges. Class II proteins access the LD surface from the cytosol and bind through amphipathic helices or other hydrophobic domains. Other proteins require lipid modifications or protein-protein interactions to bind to LDs. We summarize knowledge for targeting and removal of the different classes, and highlight areas needing investigation.Entities:
Keywords: amphipathic α-helix; hydrophobic hairpin; lipolysis; organelle protein composition; triglyceride storage
Mesh:
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Year: 2016 PMID: 26995697 PMCID: PMC4976449 DOI: 10.1016/j.tcb.2016.02.007
Source DB: PubMed Journal: Trends Cell Biol ISSN: 0962-8924 Impact factor: 20.808