The intermembrane ceramide transport catalyzed by CERT is sensitive to the lipid environment

被引:20
作者
Tuuf, Jessica [1 ]
Kjellberg, Matti A. [1 ]
Molotkovslcy, Julian G. [2 ]
Hanada, Kentaro [3 ]
Mattjus, Peter [1 ]
机构
[1] Abo Akad Univ, Dept Biosci, FI-20520 Turku, Finland
[2] Russian Acad Sci, Shemyakin Ovchinnikov Inst Bioorgan Chem, Moscow, Russia
[3] Natl Inst Infect Dis, Dept Biochem & Cell Biol, Tokyo, Japan
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES | 2011年 / 1808卷 / 01期
基金
芬兰科学院; 俄罗斯基础研究基金会;
关键词
CERT; Ceramide; Resonance energy transfer; Substrate specificity; Phosphatidylinositol; 4-monophosphate; Lipid transfer; MEDIATED GLYCOLIPID TRANSFER; ANTIGEN-BINDING PROTEIN; PHASE-EQUILIBRIA; NONVESICULAR TRAFFICKING; ENDOPLASMIC-RETICULUM; MEMBRANE PENETRATION; GOODPASTURE ANTIGEN; DOMAIN FORMATION; CHOLESTEROL; PHOSPHOLIPIDS;
D O I
10.1016/j.bbamem.2010.09.011
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The in vitro activity of the ceramide transporter, CERT has been studied using a fluorescence assay. CERT is responsible for the in vivo non-vesicular trafficking of ceramide between the endoplasmic reticulum and Golgi. In this study we have examined how the membrane environment surrounding the ceramide substrate, the membrane packing density and the membrane charge, are affecting the ceramide transfer activity. To examine this we have used an anthrylvinyl-labeled ceramide analogue. We found that if ceramide is in a tightly packed environment such as in sphingomyelin or dipalmitoylphosphatidylcholine containing membranes, the CERT transfer activity is markedly reduced. Ceramide in fluid membranes on the other hand are available for CERT mediated transfer. CERT also favors membranes that contain phosphatidylinositol 4-monophospate, due to its binding capacity of the pleckstrin homology domain towards phosphatidylinositol 4-monophospate. From this study we conclude that the membrane matrix surrounding ceramide, that is ceramide miscibility, is largely affecting the transfer activity of CERT. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:229 / 235
页数:7
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