Characterization of the Drosophila lipid droplet subproteome

被引:219
作者
Beller, Mathias
Riedel, Dietmar
Jaensch, Lothar
Dieterich, Guido
Wehland, Juergen
Jaeckle, Herbert
Kuehnlein, Ronald P.
机构
[1] Max Planck Inst Biophys Chem, Abt Mol Entwicklungsbiol, D-37077 Gottingen, Germany
[2] Max Planck Inst Biophys Chem, Abt Neurobiol, D-37077 Gottingen, Germany
[3] Gesell Biotechnol Forsch mbH, Abt Zellbiol, D-38124 Braunschweig, Germany
关键词
D O I
10.1074/mcp.M600011-MCP200
中图分类号
Q5 [生物化学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Lipid storage droplets are universal organelles essential for the cellular and organismal lipometabolism including energy homeostasis. Despite their apparently simple design they are proposed to participate in a growing number of cellular processes, raising the question to what extent the functional multifariousness is reflected by a complex organellar proteome composition. Here we present 248 proteins identified in a subproteome analysis using lipid storage droplets of Drosophila melanogaster fat body tissue. In addition to previously known lipid droplet-associated PAT (Perilipin, ADRP, and TIP47) domain proteins and homologues of several mammalian lipid droplet proteins, this study identified a number of proteins of diverse biological function, including intracellular trafficking supportive of the dynamic and multifaceted character of these organelles. We performed intracellular localization studies on selected newly identified subproteome members both in tissue culture cells and in fat body cells directly. The results suggest that the lipid droplets of fat body cells are of combinatorial protein composition. We propose that subsets of lipid droplets within single cells are characterized by a protein '' zip code,'' which reflects functional differences or specific metabolic states.
引用
收藏
页码:1082 / 1094
页数:13
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