Literature DB >> 32730754

Determinants of Endoplasmic Reticulum-to-Lipid Droplet Protein Targeting.

Maria-Jesus Olarte1, Siyoung Kim2, Morris E Sharp3, Jessica M J Swanson4, Robert V Farese5, Tobias C Walther6.   

Abstract

Lipid droplet (LD) formation from the endoplasmic reticulum (ER) is accompanied by the targeting and accumulation of specific hydrophobic, membrane-embedded proteins on LDs. The determinants of this process are unknown. Here, we study the hydrophobic membrane motifs of two Drosophila melanogaster proteins, GPAT4 and ALG14, that utilize this pathway, and we identify crucial sequence features that mediate LD accumulation. Molecular dynamics simulations and studies in cells reveal that LD targeting of these motifs requires deeply inserted tryptophans that have lower free energy in the LD oil phase and positively charged residues near predicted hairpin hinges that become less constrained in the LD environment. Analyzing hydrophobic motifs from similar LD-targeting proteins, it appears that the distribution of tryptophan and positively charged residues distinguishes them from non-LD-targeting membrane motifs. Our studies identify specific sequence features and principles of hydrophobic membrane motifs that mediate their accumulation on LDs.
Copyright © 2020 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  LiveDrop; UDP-N-acetylglucosaminyltransferase subunit; endoplasmic reticulum; glycerol-3-phosphate acyltransferase 4; lipid droplets; protein targeting

Year:  2020        PMID: 32730754      PMCID: PMC7696655          DOI: 10.1016/j.devcel.2020.07.001

Source DB:  PubMed          Journal:  Dev Cell        ISSN: 1534-5807            Impact factor:   12.270


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