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Lipid signaling protocols

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    Book Overview
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    Chapter 1 Method for Assaying the Lipid Kinase Phosphatidylinositol-5-phosphate 4-kinase α in Quantitative High-Throughput Screening (qHTS) Bioluminescent Format
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    Chapter 2 Assaying Ceramide Synthase Activity In Vitro and in Living Cells Using Liquid Chromatography-Mass Spectrometry
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    Chapter 3 Lipid Signaling Protocols
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    Chapter 4 Identification of the Interactome of a Palmitoylated Membrane Protein, Phosphatidylinositol 4-Kinase Type II Alpha
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    Chapter 5 Measurement of Long-Chain Fatty Acyl-CoA Synthetase Activity
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    Chapter 6 Qualitative and Quantitative In Vitro Analysis of Phosphatidylinositol Phosphatase Substrate Specificity
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    Chapter 7 Luciferase Reporter Assays to Assess Liver X Receptor Transcriptional Activity
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    Chapter 8 Metabolically Biotinylated Reporters for Electron Microscopic Imaging of Cytoplasmic Membrane Microdomains
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    Chapter 9 Fluorescence Recovery After Photobleaching Analysis of the Diffusional Mobility of Plasma Membrane Proteins: HER3 Mobility in Breast Cancer Cell Membranes.
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    Chapter 10 Isolation and Analysis of Detergent-Resistant Membrane Fractions
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    Chapter 11 Detection of Isolated Mitochondria-Associated ER Membranes Using the Sigma-1 Receptor
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    Chapter 12 Using Surface Plasmon Resonance to Quantitatively Assess Lipid–Protein Interactions
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    Chapter 13 Analyzing Protein–Phosphoinositide Interactions with Liposome Flotation Assays
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    Chapter 14 High-Throughput Fluorometric Assay for Membrane–Protein Interaction
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    Chapter 15 Guidelines for the Use of Protein Domains in Acidic Phospholipid Imaging.
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    Chapter 16 Analysis of Sphingolipid Synthesis and Transport by Metabolic Labeling of Cultured Cells with [ 3 H]Serine
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    Chapter 17 Determination and Characterization of Tetraspanin-Associated Phosphoinositide-4 Kinases in Primary and Neoplastic Liver Cells
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    Chapter 18 Analysis of the Phosphoinositide Composition of Subcellular Membrane Fractions
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    Chapter 19 Single-Molecule Imaging of Signal Transduction via GPI-Anchored Receptors
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    Chapter 20 Measuring Phosphatidylinositol Generation on Biological Membranes
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    Chapter 21 Assay for CDP-Diacylglycerol Generation by CDS in Membrane Fractions
Attention for Chapter 15: Guidelines for the Use of Protein Domains in Acidic Phospholipid Imaging.
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Chapter title
Guidelines for the Use of Protein Domains in Acidic Phospholipid Imaging.
Chapter number 15
Book title
Lipid Signaling Protocols
Published in
Methods in molecular biology, January 2016
DOI 10.1007/978-1-4939-3170-5_15
Pubmed ID
Book ISBNs
978-1-4939-3169-9, 978-1-4939-3170-5
Authors

Platre, Matthieu Pierre, Jaillais, Yvon, Matthieu Pierre Platre, Yvon Jaillais

Abstract

Acidic phospholipids are minor membrane lipids but critically important for signaling events. The main acidic phospholipids are phosphatidylinositol phosphates (PIPs also known as phosphoinositides), phosphatidylserine (PS), and phosphatidic acid (PA). Acidic phospholipids are precursors of second messengers of key signaling cascades or are second messengers themselves. They regulate the localization and activation of many proteins, and are involved in virtually all membrane trafficking events. As such, it is crucial to understand the subcellular localization and dynamics of each of these lipids within the cell. Over the years, several techniques have emerged in either fixed or live cells to analyze the subcellular localization and dynamics of acidic phospholipids. In this chapter, we review one of them: the use of genetically encoded biosensors that are based on the expression of specific lipid binding domains (LBDs) fused to fluorescent proteins. We discuss how to design such sensors, including the criteria for selecting the lipid binding domains of interest and to validate them. We also emphasize the care that must be taken during data analysis as well as the main limitations and advantages of this approach.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 47 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 47 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 19 40%
Researcher 5 11%
Student > Master 5 11%
Student > Postgraduate 4 9%
Student > Doctoral Student 3 6%
Other 6 13%
Unknown 5 11%
Readers by discipline Count As %
Agricultural and Biological Sciences 17 36%
Biochemistry, Genetics and Molecular Biology 14 30%
Chemistry 4 9%
Immunology and Microbiology 1 2%
Medicine and Dentistry 1 2%
Other 3 6%
Unknown 7 15%