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High-Throughput Screening Assays in Toxicology

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Cover of 'High-Throughput Screening Assays in Toxicology'

Table of Contents

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    Book Overview
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    Chapter 1 Monitoring Ligand-Activated Protein–Protein Interactions Using Bioluminescent Resonance Energy Transfer (BRET) Assay
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    Chapter 2 Mitochondrial Membrane Potential Assay
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    Chapter 3 High-Throughput Screening Assays in Toxicology
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    Chapter 4 Quantitative High-Throughput Luciferase Screening in Identifying CAR Modulators
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    Chapter 5 Transactivation and Coactivator Recruitment Assays for Measuring Farnesoid X Receptor Activity
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    Chapter 6 Cell-Based Assay for Identifying the Modulators of Antioxidant Response Element Signaling Pathway
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    Chapter 7 Study Liver Cytochrome P450 3A4 Inhibition and Hepatotoxicity Using DMSO-Differentiated HuH-7 Cells
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    Chapter 8 Determination of Histone H2AX Phosphorylation in DT40 Cells
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    Chapter 9 High-Throughput and High-Content Micronucleus Assay in CHO-K1 Cells
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    Chapter 10 High-Throughput Screening Assays in Toxicology
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    Chapter 11 High-Throughput Screening Assays in Toxicology
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    Chapter 12 A Quantitative High-Throughput Screening Data Analysis Pipeline for Activity Profiling
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    Chapter 13 Correction of Microplate Data from High-Throughput Screening
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    Chapter 14 CurveP Method for Rendering High-Throughput Screening Dose-Response Data into Digital Fingerprints
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    Chapter 15 Accounting Artifacts in High-Throughput Toxicity Assays
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    Chapter 16 Accessing the High-Throughput Screening Data Landscape
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    Chapter 17 Curating and Preparing High-Throughput Screening Data for Quantitative Structure-Activity Relationship Modeling
Attention for Chapter 1: Monitoring Ligand-Activated Protein–Protein Interactions Using Bioluminescent Resonance Energy Transfer (BRET) Assay
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Chapter title
Monitoring Ligand-Activated Protein–Protein Interactions Using Bioluminescent Resonance Energy Transfer (BRET) Assay
Chapter number 1
Book title
High-Throughput Screening Assays in Toxicology
Published in
Methods in molecular biology, January 2016
DOI 10.1007/978-1-4939-6346-1_1
Pubmed ID
Book ISBNs
978-1-4939-6344-7, 978-1-4939-6346-1
Authors

Carlos Coriano, Emily Powell, Wei Xu, Coriano, Carlos, Powell, Emily, Xu, Wei

Editors

Hao Zhu, Menghang Xia

Abstract

The bioluminescent resonance energy transfer (BRET) assay has been extensively used in cell-based and in vivo imaging systems for detecting protein-protein interactions in the native environment of living cells. These protein-protein interactions are essential for the functional response of many signaling pathways to environmental chemicals. BRET has been used as a toxicological tool for identifying chemicals that either induce or inhibit these protein-protein interactions. This chapter focuses on describing the toxicological applications of BRET and its optimization as a high-throughput detection system in live cells. Here we review the construction of BRET fusion proteins, describe the BRET methodology, and outline strategies to overcome obstacles that may arise. Furthermore, we describe the advantage of BRET over other resonance energy transfer methods for monitoring protein-protein interactions.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 15 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 15 100%

Demographic breakdown

Readers by professional status Count As %
Student > Master 4 27%
Student > Bachelor 3 20%
Professor 2 13%
Student > Doctoral Student 1 7%
Other 1 7%
Other 0 0%
Unknown 4 27%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 3 20%
Agricultural and Biological Sciences 2 13%
Pharmacology, Toxicology and Pharmaceutical Science 2 13%
Medicine and Dentistry 2 13%
Chemical Engineering 1 7%
Other 1 7%
Unknown 4 27%