Quantifying lipid changes in various membrane compartments using lipid binding protein domains

被引:40
|
作者
Varnai, Peter [2 ]
Gulyas, Gergo [2 ]
Toth, Daniel J. [1 ,2 ]
Sohn, Mira [1 ]
Sengupta, Nivedita [1 ]
Balla, Tamas [1 ]
机构
[1] NICHHD, Sect Mol Signal Transduct, Program Dev Neurosci, NIH, Bethesda, MD 20892 USA
[2] Semmelweis Univ, Dept Physiol, Fac Med, Budapest, Hungary
基金
美国国家卫生研究院;
关键词
Phospholipid; Phosphoinositide; Membrane; PH domain; Phospholipase C; PX domain; FYVE domain; Fluorescent imaging; TIRF microscopy; BRET analysis; FRET analysis; Confocal microscopy; PLECKSTRIN-HOMOLOGY-DOMAIN; IMAGING PHOSPHOINOSITIDE DYNAMICS; KINASE C-EPSILON; PLASMA-MEMBRANE; PHOSPHATIDIC-ACID; PHOSPHATIDYLINOSITOL 4,5-BISPHOSPHATE; PX DOMAIN; ER-PM; CRYSTAL-STRUCTURE; SUBCELLULAR-LOCALIZATION;
D O I
10.1016/j.ceca.2016.12.008
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
One of the largest challenges in cell biology is to map the lipid composition of the membranes of various organelles and define the exact location of processes that control the synthesis and distribution of lipids between cellular compartments. The critical role of phosphoinositides, low -abundant lipids with rapid metabolism and exceptional regulatory importance in the control of almost all aspects of cellular functions created the need for tools to visualize their localizations and dynamics at the single cell level. However, there is also an increasing need for methods to determine the cellular distribution of other lipids regulatory or structural, such as diacylglycerol, phosphatidic acid, or other phospholipids and cholesterol. This review will summarize recent advances in this research field focusing on the means by which changes can be described in more quantitative terms. Published by Elsevier Ltd.
引用
收藏
页码:72 / 82
页数:11
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