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Structure and function of lipid droplet assembly complexes
Affiliation:1. Cell Biology Program, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, USA;2. Howard Hughes Medical Institute, New York, NY 10065, USA;3. Pritzker School of Molecular Engineering, University of Chicago, Chicago, IL, 60637, USA;4. Department of Chemistry, Chicago Center for Theoretical Chemistry, James Franck Institute, and Institute for Biophysical Dynamics, University of Chicago, Chicago, IL, 60637, USA
Abstract:Cells store lipids as a reservoir of metabolic energy and membrane component precursors in organelles called lipid droplets (LDs). LD formation occurs in the endoplasmic reticulum (ER) at LD assembly complexes (LDAC), consisting of an oligomeric core of seipin and accessory proteins. LDACs determine the sites of LD formation and are required for this process to occur normally. Seipin oligomers form a cage-like structure in the membrane that may serve to facilitate the phase transition of neutral lipids in the membrane to form an oil droplet within the LDAC. Modeling suggests that, as the LD grows, seipin anchors it to the ER bilayer and conformational shifts of seipin transmembrane segments open the LDAC dome toward the cytoplasm, enabling the emerging LD to egress from the ER.
Keywords:Triacylglycerol  Sterol esters  Seipin  Endoplasmic reticulum  Lipid droplet  Phospholipids  Surface tension  Phase separation
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