Kory Nora, Farese Robert V, Walther Tobias C
Department of Genetics and Complex Diseases, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Department of Genetics and Complex Diseases, Harvard T.H. Chan School of Public Health, Boston, MA, USA; Department of Cell Biology, Harvard Medical School, Boston, MA, USA; Broad Institute of Massachusetts Institute of Technology (MIT) and Harvard, Cambridge, MA, USA.
Trends Cell Biol. 2016 Jul;26(7):535-546. doi: 10.1016/j.tcb.2016.02.007. Epub 2016 Mar 16.
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.
蛋白质如何特异性地定位于脂滴(LDs)的磷脂单分子层表面正在被逐步揭示。我们在此回顾蛋白质靶向LDs的主要已知途径,并基于蛋白质的定位起源提出一个分类框架。I类蛋白质通常具有膜嵌入的疏水“发夹”基序,在LDs形成过程中或形成后通过内质网(ER)-LD膜桥从内质网进入LDs。II类蛋白质从细胞质溶胶进入LD表面,并通过两亲性螺旋或其他疏水域结合。其他蛋白质需要脂质修饰或蛋白质-蛋白质相互作用才能与LDs结合。我们总结了针对不同类别蛋白质的靶向和去除的相关知识,并突出了需要研究的领域。