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Kinase Screening and Profiling

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Cover of 'Kinase Screening and Profiling'

Table of Contents

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    Book Overview
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    Chapter 1 HTRF Kinase Assay Development and Methods in Inhibitor Characterization
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    Chapter 2 Application of Eukaryotic Elongation Factor-2 Kinase (eEF-2K) for Cancer Therapy: Expression, Purification, and High-Throughput Inhibitor Screening
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    Chapter 3 Recombinant Kinase Production and Fragment Screening by NMR Spectroscopy.
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    Chapter 4 Bioluminescence Methods for Assaying Kinases in Quantitative High-Throughput Screening (qHTS) Format Applied to Yes1 Tyrosine Kinase, Glucokinase, and PI5P4Kα Lipid Kinase
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    Chapter 5 Using Bioluminescent Kinase Profiling Strips to Identify Kinase Inhibitor Selectivity and Promiscuity
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    Chapter 6 Measuring Activity of Phosphoinositide Lipid Kinases Using a Bioluminescent ADP-Detecting Assay.
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    Chapter 7 A High-Throughput Radiometric Kinase Assay
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    Chapter 8 A High-Content Assay to Screen for Modulators of EGFR Function
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    Chapter 9 Monitoring Protein Kinase Expression and Phosphorylation in Cell Lysates with Antibody Microarrays
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    Chapter 10 From Enzyme to Whole Blood: Sequential Screening Procedure for Identification and Evaluation of p38 MAPK Inhibitors.
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    Chapter 11 Genetically Encoded Fluorescent Indicators to Visualize Protein Phosphorylation in Living Cells
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    Chapter 12 Characterization of an Engineered Src Kinase to Study Src Signaling and Biology
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    Chapter 13 Screening One-Bead-One-Compound Peptide Libraries for Optimal Kinase Substrates
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    Chapter 14 Determination of the Substrate Specificity of Protein Kinases with Peptide Micro- and Macroarrays
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    Chapter 15 Rapid Identification of Protein Kinase Phosphorylation Site Motifs Using Combinatorial Peptide Libraries
Attention for Chapter 6: Measuring Activity of Phosphoinositide Lipid Kinases Using a Bioluminescent ADP-Detecting Assay.
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Chapter title
Measuring Activity of Phosphoinositide Lipid Kinases Using a Bioluminescent ADP-Detecting Assay.
Chapter number 6
Book title
Kinase Screening and Profiling
Published in
Methods in molecular biology, January 2016
DOI 10.1007/978-1-4939-3073-9_6
Pubmed ID
Book ISBNs
978-1-4939-3072-2, 978-1-4939-3073-9
Authors

Tai, Andrew W, Vidugiriene, Jolanta, Andrew W. Tai, Jolanta Vidugiriene

Abstract

Phosphatidylinositol (PI) and its phosphorylated derivatives, collectively called phosphoinositides, are important second messengers involved in a variety of cellular processes, including cell proliferation, apoptosis, metabolism, and migration. These derivatives are generated by a family of kinases called phosphoinositide lipid kinases (PIKs). Due to the central role of these kinases in signaling pathways, assays for measuring their activity are often used for drug development. Lipid kinase substrates are present in unique membrane environments in vivo and are insoluble in aqueous solutions. Therefore the most important consideration in developing successful lipid kinase assays is the physical state of lipid kinase substrates. Here we describe the preparation of lipid substrates for two major classes of lipid kinases, phosphatidylinositol 3-kinases (PI3Ks) and phosphatidylinositol 4-kinases (PI4Ks). Using PI4Ks as an example, we also provide a detailed protocol for small-scale kinase expression and affinity purification from transiently transfected mammalian cells. For measuring lipid kinase activity we apply a universal bioluminescent ADP detection approach. The approach is compatible with diverse lipid substrates and can be used as a single integrated platform for measuring all classes of lipid and protein kinases.

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The data shown below were compiled from readership statistics for 2 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 2 100%

Demographic breakdown

Readers by professional status Count As %
Professor > Associate Professor 1 50%
Student > Bachelor 1 50%
Readers by discipline Count As %
Neuroscience 1 50%
Medicine and Dentistry 1 50%