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Lipid signaling protocols

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Table of Contents

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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 20: Measuring Phosphatidylinositol Generation on Biological Membranes
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Chapter title
Measuring Phosphatidylinositol Generation on Biological Membranes
Chapter number 20
Book title
Lipid Signaling Protocols
Published in
Methods in molecular biology, January 2016
DOI 10.1007/978-1-4939-3170-5_20
Pubmed ID
Book ISBNs
978-1-4939-3169-9, 978-1-4939-3170-5
Authors

Mark G. Waugh

Abstract

Phosphatidylinositol (PI) is a phospholipid molecule required for the generation of seven different phosphoinositide lipids which have a diverse range of signaling and trafficking functions. The precise mechanism of phosphatidylinositol supply during receptor activated signaling and the cellular compartmentation of the synthetic process are still incompletely understood and remain controversial despite several decades of research in this area. The synthesis of phosphatidylinositol requires the activity of an enzyme called phosphatidylinositol synthase, also known as CDIPT, which catalyzes a reversible headgroup exchange reaction on its substrate liponucleotide CDP-diacylglycerol resulting in the incorporation of inositol to generate phosphatidylinositol and the release of CMP. This protocol describes a method for locating PI synthase activity in isolated, intact biological membranes and vesicles.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 5 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 5 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 3 60%
Student > Master 1 20%
Unknown 1 20%
Readers by discipline Count As %
Agricultural and Biological Sciences 3 60%
Medicine and Dentistry 1 20%
Unknown 1 20%