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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 4: Quantitative High-Throughput Luciferase Screening in Identifying CAR Modulators
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Chapter title
Quantitative High-Throughput Luciferase Screening in Identifying CAR Modulators
Chapter number 4
Book title
High-Throughput Screening Assays in Toxicology
Published in
Methods in molecular biology, January 2016
DOI 10.1007/978-1-4939-6346-1_4
Pubmed ID
Book ISBNs
978-1-4939-6344-7, 978-1-4939-6346-1
Authors

Caitlin Lynch, Jinghua Zhao, Hongbing Wang, Menghang Xia, Lynch, Caitlin, Zhao, Jinghua, Wang, Hongbing, Xia, Menghang

Abstract

The constitutive androstane receptor (CAR, NR1I3) is responsible for the transcription of multiple drug metabolizing enzymes and transporters. There are two possible methods of activation for CAR, direct ligand binding and a ligand-independent method, which makes this a unique nuclear receptor. Both of these mechanisms require translocation of CAR from the cytoplasm into the nucleus. Interestingly, CAR is constitutively active in immortalized cell lines due to the basal nuclear location of this receptor. This creates an important challenge in most in vitro assay models because immortalized cells cannot be used without inhibiting the high basal activity. In this book chapter, we go into detail of how to perform quantitative high-throughput screens to identify hCAR1 modulators through the employment of a double stable cell line. Using this line, we are able to identify activators, as well as deactivators, of the challenging nuclear receptor, CAR.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 6 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 6 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 2 33%
Researcher 2 33%
Student > Bachelor 1 17%
Other 1 17%
Readers by discipline Count As %
Pharmacology, Toxicology and Pharmaceutical Science 2 33%
Agricultural and Biological Sciences 1 17%
Computer Science 1 17%
Medicine and Dentistry 1 17%
Neuroscience 1 17%
Other 0 0%