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G Protein-Coupled Receptors in Drug Discovery

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Cover of 'G Protein-Coupled Receptors in Drug Discovery'

Table of Contents

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    Book Overview
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    Chapter 1 Purification of Stabilized GPCRs for Structural and Biophysical Analyses
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    Chapter 2 Purification and Crystallization of a Thermostabilized Agonist-Bound Conformation of the Human Adenosine A 2A Receptor
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    Chapter 3 2D Projection Analysis of GPCR Complexes by Negative Stain Electron Microscopy
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    Chapter 4 Nuts and Bolts of CF 3 and CH 3 NMR Toward the Understanding of Conformational Exchange of GPCRs
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    Chapter 5 Single-Molecule Fluorescence Microscopy for the Analysis of Fast Receptor Dynamics
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    Chapter 6 Quantitative Multi-color Detection Strategies for Bioorthogonally Labeled GPCRs
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    Chapter 7 Approaches to Characterize and Quantify Oligomerization of GPCRs
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    Chapter 8 Monitoring G Protein Activation in Cells with BRET
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    Chapter 9 Use of Fluorescence Indicators in Receptor Ligands
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    Chapter 10 Detection and Quantification of Intracellular Signaling Using FRET-Based Biosensors and High Content Imaging
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    Chapter 11 The Measurement of Receptor Signaling Bias
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    Chapter 12 Approaches to Assess Functional Selectivity in GPCRs: Evaluating G Protein Signaling in an Endogenous Environment
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    Chapter 13 Bioluminescence Resonance Energy Transfer Approaches to Discover Bias in GPCR Signaling
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    Chapter 14 Virus-Mediated Expression of DREADDs for In Vivo Metabolic Studies
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    Chapter 15 High-Throughput Screening for Allosteric Modulators of GPCRs
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    Chapter 16 Radioligand Binding Assay for an Exon 11-Associated Mu Opioid Receptor Target
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    Chapter 17 Docking and Virtual Screening Strategies for GPCR Drug Discovery
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    Chapter 18 The Dynamic Process of Drug–GPCR Binding at Either Orthosteric or Allosteric Sites Evaluated by Metadynamics
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    Chapter 19 Experiment-Guided Molecular Modeling of Protein–Protein Complexes Involving GPCRs
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    Chapter 20 Interaction Fingerprints and Their Applications to Identify Hot Spots
Attention for Chapter 9: Use of Fluorescence Indicators in Receptor Ligands
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Chapter title
Use of Fluorescence Indicators in Receptor Ligands
Chapter number 9
Book title
G Protein-Coupled Receptors in Drug Discovery
Published in
Methods in molecular biology, January 2015
DOI 10.1007/978-1-4939-2914-6_9
Pubmed ID
Book ISBNs
978-1-4939-2913-9, 978-1-4939-2914-6
Authors

Kaleeckal G. Harikumar, Laurence J. Miller, Harikumar, Kaleeckal G., Miller, Laurence J.

Abstract

Fluorescence techniques can provide insights into the environment of fluorescence indicators incorporated within a ligand as it is bound to its receptor. Fluorescence indicators of different sizes and chemical characteristics can provide insights into the nature of the binding environment, the surrounding structures, and even into conformational changes associated with receptor activation. Methods for determining fluorescence spectral analysis, fluorescence quenching, fluorescence anisotropy, fluorescence lifetimes, and red edge excitation shifts of the ligand probes are described. The applications of these techniques to the CCK1 receptor occupied by alexa(488)-CCK and aladan-CCK, as examples of probes developed (1) by derivatization of an existing peptide and (2) by incorporation during peptide synthesis, are utilized as examples. These methods represent powerful tools to expand our understanding of the structure and molecular basis of ligand activation of G protein-coupled receptors.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 13 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Sweden 1 8%
Unknown 12 92%

Demographic breakdown

Readers by professional status Count As %
Researcher 5 38%
Student > Ph. D. Student 3 23%
Student > Master 2 15%
Lecturer > Senior Lecturer 1 8%
Unknown 2 15%
Readers by discipline Count As %
Agricultural and Biological Sciences 4 31%
Biochemistry, Genetics and Molecular Biology 3 23%
Medicine and Dentistry 3 23%
Chemistry 1 8%
Unknown 2 15%